http://www.newscientistjobs.com/jobsNew Scientist Jobshttp://www.newscientistjobs.com/jobs/job/clinical-sas-programmer-homebased-surrey-200645894.htmSat, 21 Nov 2009 08:00:52 +0000199238Clinical SAS Programmer Homebased Fantastic opportunities are now available for experienced SAS programmers to work for a market leading Clinical Research Organisastion. This rapidly expanding CRO is on the lookout for Clinical SAS Programmers with a solid background of CDISC to join their established biostatistics department. Successful candidates will have the option of being based in a variety of European offices or working from home depending on your individual situation. As the SAS programmer you will be expected to provide SAS programming support on a variety of team projects, within all phases of the drugs development process. This will include supporting the production of statistical summaries for clinical trials, patient data listings, summary tables and figures using SAS tools. In addition you will be expected to ensure the quality of these statistical summaries, data listings and graphs, monitoring them for any inconsistencies and implementing the validation process. You will also ensure that all projects meet with the client's specific time lines and budgets. The ideal candidate will have a strong bachelor's degree in statistics or quantitative discipline with a minimum of 2 years SAS programming experience for a clinical research organisation or pharmaceutical company. You will be expected to have a good knowledge or ICP-GCP alongside excellent interpersonal and communication skills. Please note: This role is a homebased opportunity and previous experience in SAS programming within a CRO is essential. In return you will receive a generous salary and competitive benefits packages, including flexible working hours and much more. For more information please call Kieron Mcdaid on 0121 616 3462 Keywords: SAS, Programming, Clinical, Life Science, Biostatistics, Drug Development Paramount Recruitment Limited provides services as an agency and an employment business. We regularly have similar roles in this area. Please see our website for details or send your CV in to us to find out the latest opportunities. http://www.newscientistjobs.com/jobs/job/clinical-research-nurse-204951-ca-california-200645879.htmFri, 20 Nov 2009 22:11:28 +0000196404The Henry M. Jackson Foundation (HJF) is seeking a Clinical Research Nurse to support the Clinical Investigation Department located at the Naval Medical Center in San Diego (NMCSD), California. HJF provides administrative and management support to NMC. Naval Medical Center San Diego (NMCSD) is the most technologically advanced Navy medical treatment facility. Nicknamed, Balboa, the Pride of Navy Medicine, the hospital has played a vital role in the history of San Diego for more than 80 years. From the original tent dispensary established in 1917, to the high-tech, ultra modern facility of the 1990's, the mission has remained constant to provide the finest medical care in a family-centered care environment to the operational forces, their families, and to those who served their country in the past. Responsibilities: 1. Studies document creation, including protocols, amendments, consent forms, data collection and date collection forms. 2. Conducts patient interviews, patient recruitment, enrollment, and verifies patient eligibility for the clinical investigative studies. 3. Observes patients after administration of study medication for adverse events, takes and properly records vital signs, performs venipuncture, and specimen collection and processing. 4. Completes case report forms, maintains data research logs, schedules appointments, prepares patient recruitment letters, and various other study correspondence. 5. Maintains weekly/monthly status reports on all patients. 6. Educates patients about clinical research protocols, study requirements and expectations. 7. Adheres to legal, professional and ethical codes with respect to confidentiality and privacy. 8. Recruits, manages and schedules all study site personnel as required and assists in the department’s clinical activities as required to support the research effort. 9. May analyze and interpret data. 10. Travels for project meetings, related conferences, and site visits, as required. 11. Performs other duties as needed. Required Knowledge, Skills, and Abilities: Knowledge of procedures and techniques necessary for performing research tasks; ability to learn and become proficient in data acquisition and clinical responsibilities related to research protocols; excellent interpersonal skills. Minimum Education/Training Requirements: Bachelor's degree in nursing Minimum Experience: 2 to 4 years nursing experience, at least 1 year in clinical research care. Physical Capabilities: Long periods of sitting, standing, escorting patients, carrying light items; may encounter patients who are confused, agitated, or abusive Required Licenses, Certification or Registration: Licensed as a Registered Nurse, certified in basic cardiac life support Work Environment: Office and clinical patient care area; possible evening and/or weekend hours. Please apply on-line at www.hjf.org/careers Click “Advanced Search” and enter job number 204951 in the Job Opening ID box. OR fax your resume to 240-314-7334. Please specify title and job number on fax. HJF is a nonprofit medical research organization that provides support services to the military medical community and offers a competitive salary and generous benefits package. AA/EEO For a comprehensive list of our benefits, please visit: http://www.hjf.org/careers/benefits.html HJF administers innovative medical research, supports education and training, and facilitates collaborations between the military and private medical communities. We provide comprehensive management and scientific services for more than 1,000 basic, clinical and applied research projects conducted around the globe. We also support continuing medical education programs for more than 160 military medical research and treatment facilities, and military medical organizations. http://www.newscientistjobs.com/jobs/job/senior-research-associate-philadelphia-pa-pa-pennsylvania-200631302.htmFri, 20 Nov 2009 22:08:16 +0000196398Senior Research Associate, Philadelphia, PA No relocation! For consideration, applicants must be located near the Philadelphia, PA area. Description: Under the direction of the Director of the Immunology Laboratory, to promote and coordinate the multiple aspects of the growing research program of immunology Laboratory. The job involves performing diverse and complex clinical research activities including, but not limited to, writing study protocols and other research related documents, maintaining IRB and GCRC approval of study protocols, creating and instituting quality assurance procedures, performing research quality bone age and bone mineral density determinations, data management and quantitative analysis, collaborating in developing innovative research and educational programs, writing manuscripts and grant proposals, coordinating activities in multi-center studies, and serving as an educational resource for the laboratory and the Institution. This position has the potential for the candidate to develop into an independent investigator. Qualifications: MD or Ph.D. or equivalent in Immunology or related field with 2 years of experience in pediatric stress/psychometric biomarkers. Previous experience in cell culture, Elisa and PCR preferred. Ability to function independently in a clinical research setting. Excellent writing skills. Excellent communication skills to interact with staff, parents and children. Ability to handle confidential materials. Ability to handle multiple, time dependent tasks. Excellent organizational skills. Ability to use computers, learn new software applications. Ability to manage data and perform quantitative analysis. Ability to write progress reports and scientific manuscripts. To apply please send your CV and three letters of recommendation to Wendy Rochlin by clicking Apply Now. http://www.newscientistjobs.com/jobs/job/technical-delivery-manager-md-maryland-200642313.htmFri, 20 Nov 2009 22:00:00 +0000196373My company shares my passion for helping to improve human health around the world. This is My MedImmune. Those who join MedImmune feel a sense of ownership about their future. They thrive with a recognized leader in the biotechnology industry and the wholly-owned subsidiary of AstraZeneca plc. Here, you will join passionate professionals who advance science, technology and medicine to develop products designed to help people live better lives. You will excel in an environment characterized by respect, integrity and growth opportunities that encourages both individual contribution and collaborative entrepreneurial thinking. Our products and/or product candidates are designed to address areas of need in infection, oncology, respiratory disease and inflammation, cardiovascular/gastrointestinal disease and neuroscience. Explore a MedImmune career as we strive to better more lives, more often, around the world. Title: Technical Delivery Manager Location: MD, Gaithersburg - Corporate Headquarters Req: 02109 Job Description Position will work in IT addressing the business technology needs within the area of Medical and Regulatory Affairs. Position will be responsible for understanding business problems and working with relationship managers, business analysts and technical teams to develop technology solutions in support of business needs. In addition, position will be responsible for overseeing technology solutions; implementing system-based solutions; and managing vendor partners and internal resources in the delivery and support of technology to satisfy MedImmune's business capability needs. Position will be responsible for technical oversight and management of projects. Position will own technical requirements definition based on functional requirements and taking the solution blueprint, in conjunction with the user requirements, and turning it into a detailed design or configuration. Position will assess the scope of new project efforts by estimating the work involved, resources required and time line for technical delivery efforts. Position owns solution prototyping and change management, blueprinting (fit/gap) and quality assurance; manages the development and delivery activities within SDD in support of project and non-project activities. Has direct responsibility for the overall success of the assigned project and deliverables, either through direct participation or oversight. Projects may include new applications and modules, major or minor enhancements to existing applications or modules and product upgrades. Position will work with business owners, relationship managers and IT to manage the development to production and the production to operations activities following established methodology. Activities include internal code reviews, testing, supporting user acceptance testing, developing a support approach, application training, disaster recovery plans, application process maps and others as defined by the IT PMO. Position will keep customers (to include business owners, relationship managers, and internal IT management) apprised of progress, issues, and risks in a timely manner. Position will practice risk management strategies to ensure that project commitments are realistic and met. Position will participate in the establishment and implementation of SDLC methodologies, ITIL processes and IT PMO processes and ensure that IT projects adhere to those standards and meet customer expectations International travel may be required. Additional requirements for Medical and Regulatory Affairs include: Experience with Medical and Regulatory Affairs in a pharmaceutical or biotech environment. Clinical trials knowledge. Experience with data warehousing and data mining. Skills: Demonstrated ability to manage software development teams, implementation of off the shelf software packages, and interdependencies within an IT development organization. Demonstrated ability to manage cost, schedule, and performance of IT development projects and departments. Demonstrated ability to manage different development resources to include, internal, external, contracted staff augmentation resources, and outsourcing partners. Ability to collaborate and engage IT stakeholders including IT security, Validation/QA, IT Infrastructure, and Enterprise Architecture as needed. Proven ability to identify, manage and mitigate issues and risks. Demonstrated oral and written communication skills. Experience presenting project information in a formal and informal setting. Demonstrated focus on meeting customer expectations and working with a customer service mindset. Demonstrated interpersonal skills with experience managing diverse teams. Demonstrated ability to staff and develop individuals and teams. Demonstrated commitment to staff development and retention. Demonstrated ability to conduct facilitated sessions with end users and business owners in order to define requirements and review project progress. Demonstrated skills in problem identification, isolation and resolution through the use of analysis, troubleshooting and other like techniques. Experience coaching staff on problem resolution techniques Functional Knowledge is necessary in the following areas: Biotech or Pharmaceuticals; Validated Systems Environments; Sarbanes-Oxley Requirements; Data and Application Security; Business Intelligence Processes and Methodology knowledge is necessary in the following areas: Familiarity with ITIL; SDLC processes to include rapid and waterfall development; Project management of multiple development projects; Data Analysis. Experience with electronic publishing processes (e.g. eCTD and other formats), document management (Documentum, LiveLink, etc) is highly desirable. Technical Skills are necessary in the following areas: Application Platforms (SharePoint, SharePoint Portal Server, SharePoint Server 2007, Web Logic, IIS). Application Development (XML, WebServices, Middleware such as BizTalk or BEA Aqua Logic); MS Office Suite of Products; Database and Business Intelligence (Data warehousing, Oracle, TOAD or other similar, SQL Server, MS Access); Development Applications (Visual Studios Team Services, Development management tool such as Rational or visual studio, etc.); Programming Languages (SQL, PL/SQL, Transact-SQL, C#) JOB REQUIREMENTS: Job Requirements Education: Bachelor's degree from accredited college or university is required. Bachelor's or master's degree in computer-related curriculum is desired. Experience: 6+ years of work experience; 4-5+ years of IT work experience, with progressively more responsibility; Proven track record of managing and coordinating several projects simultaneously while delivering on time, on schedule, and meeting customer expectations; Experience project planning from project inception through transition to operational support; 1-2 years in a pharmaceutical, biotech, or consumer goods environment; 2-3 years of managing technical resources to include internal and vendor partners; Ability to provide leadership, management and technical expertise to a culturally diverse, technically-oriented staff If you are interested in this position please click the Apply Now button below and search for Req #. 02109. MedImmune is an Equal Opportunity Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, veteran status, or any other characteristic protected by federal, state or local law. http://www.newscientistjobs.com/jobs/job/medical-physicist-2194247-united-states-200644439.htmFri, 20 Nov 2009 21:35:08 +0000196372We’re Brigham and Women’s Hospital and we’re ready to show you what makes us the best place for your career. Tenth on the 2009 U.S. News & World Report honor roll of top hospitals, here you’ll find more options to expand your expertise in an environment that offers you state-of-the-art facilities, robust development programs, innovative research, and outstanding collaboration opportunities. The Medical Physics and Biophysics Division is seeking a PhD level Physicist at the Assistant or Associate Professor level to join our dynamic Physics staff of 50 people, including 12 faculty physicists. This role will support our clinical physics operation and pursue a vigorous Research and Development program at the Department of Radiation Oncology. Research areas of special interest include use of functional imaging (PET, SPECT, CT, MRI) for radiation target definition and/or treatment follow-up; SBRT treatment delivery and associated biological modeling; pre-clinical models for SBRT irradiation and functional imaging; image-guided brachytherapy; and biophysics. The division currently provides services at Brigham and Women’s Hospital, Dana-Farber Cancer Institute, Children’s Hospital at Harvard Medical School, as well as the new outreach Cancer Centers in the surrounding communities at Milford and South Shore. Our cutting-edge facilities are home to 2 Varian Novalis-Tx, 6 Varian iX/EX, 1 Novalis 6500SR, 1 HDR unit with dedicated CT scanner, a TBI unit, and 5 CT-simulators. Establishment of state-of-the art pre-clinical facilities is currently underway, as well. The ideal candidate will have a strong record of academic/or clinical achievement; board certification in Therapeutic Radiology; and a minimum 5 years of radiation oncology experience. Past leadership in the implementation of innovative technologies, high quality publications, and evidence of external funding, as well as a strong record of academic and/ or clinical achievement are highly regarded. To find out why Brigham is a better place to belong, pleas send your cover letter, CV, and a list of 3+ references to: G. Mike Makrigiorgos, PhD, Chief of Medical Physics and Biophysics, Department of Radiation Oncology, Brigham and Women’s Hospital, Harvard Medical School, 75 Francis Street, Boston, MA 02115; E-mail by clicking Apply Now or find the full mailing address below by clicking View Contact Details. Brigham and Women’s Hospital is an EEO, AA and VEVRAA employer. http://www.brighamandwomens.org/careers http://www.newscientistjobs.com/jobs/job/scientist-ii-statistician-newark-delaware-healthcare-company-de-delaware-200617896.htmFri, 20 Nov 2009 21:20:12 +0000196370Scientist II - Statistician - Newark, Delaware - Healthcare company At Nemours, we're dedicated to achieving higher standards in children's health. We've made a promise to do whatever it takes to prevent and treat even the most disabling childhood conditions. It's a promise that extends beyond our nationally recognized clinical treatment to an entire integrated spectrum of research, advocacy, education and prevention. Nemours cares for approximately a quarter of a million children annually. And we begin by caring for every child as if they were our own. For more than 70 years, this has been the Nemours Way. Nemours Health and Prevention Services (NHPS), headquartered in Newark, Delaware, works with families and communities to help children grow up healthy, both physically and emotionally. It is a division of Nemours, a non-profit organization dedicated to children's health and health care that offers treatment services, research and training programs in Delaware, New Jersey, Pennsylvania and Florida. Health and Prevention is Nemours' newest division, created to expand its reach beyond clinical care and to consider the health of the whole child within his or her family and community. NHPS' work currently focuses on health topics such as healthy eating and physical activity and on emotional/behavioral health. This work targets integration of program, practice, and policy change in four sectors in the state of Delaware: child care, schools, primary health care and communities. BENEFITS: Nemours Associates enjoy our comprehensive Total Rewards package. Here are just a few examples of the Total Rewards available to our full-time employees: *Unique to Nemours: premium-free medical and prescription drug coverage to eligible dependents of full-time Associates. *Excellent retirement plan options. *Generous continuing education (CME) program. *A broad range of specialty programs. *Competitive salaries. *Excellent health and dental benefit plans. *Tuition reimbursement. Nemours is seeking a Scientist II - Statistician to join our team in Newark, Delaware. *Perform complex computer systems analyses, including quality control, data validation and data diagnostics. *Design, document, implement and maintain complex SAS programs involving the integration of current and legacy data from a variety of file types. *Design the scope and structure of SAS datasets, Web-based applications, and electronically transmitted and hard-copy reports. *Conduct quantitative/qualitative analyses using the SAS programming language and other tools. *Maintain and refine data files and reports. *Participate in the design, development, implementation and maintenance of indicators, methodologies, processes and procedures that enable the analyses of complex data, e.g., clinical data, vital statistics data and survey data. *Analyze and interpret data, and prepare summary reports. *Participate in the ongoing monitoring of the effectiveness of evaluation and research processes. *Work with researchers within the Division, within the larger Nemours organization, and at other organizations (e.g., state data repositories and universities) to develop and implement health-related analyses. *Position has no direct reports, but may serve lead and directive roles on a project-specific basis. *Respond to ad hoc requests for information from both internal and external customers. *Prepare written reports and documentation of analytic plans and processes. *Inform internal and external customers of the technical components involved in current/proposed projects, initiatives and analyses. Requirements: *Master's degree with 3-5 years of direct experience. Apply online by clicking Apply Now Nemours is an equal opportunity employer. http://www.newscientistjobs.com/jobs/job/salk-institute-and-fondation-ipsen-present-the-4th-annual-symposium-on-biological-complexity-ca-california-200645877.htmFri, 20 Nov 2009 21:00:11 +0000196368Abstract submission deadline: December 1, 2009 Registration deadline: December 18, 2009 Salk Institute and Fondation IPSEN present The 4th Annual Symposium on Biological Complexity: Sensory Systems: Smell, Taste, Touch, Hearing and Vision January 13-15, 2010 Salk Institute, La Jolla, CA Register today! by clicking Apply Now below Each sensory system has peripheral receptors and specialized cells to translate the physical stimulus into patterns of electrical signals. Sensory systems then perform a series of common functions that allow the specific information to be integrated by the brain. This symposium brings together leaders who will discuss and compare the molecular events and higher cognition that occurs in the chemosensory, somatosensory, auditory and the visual systems. Speakers: The Sydney Brenner Nobel Lecture: Martin Chalfie Tom Albright (Salk Institute) Richard Axel (Columbia) Jean Bennett (University of Pennsylvania) Linda Buck (Fred Hutchinson Cancer Research Center) M. Catherine Bushnell (McGill) Constance Cepko (Harvard) David Corey (Harvard) Stefan Heller (Stanford) David Julius (UC San Francisco) Andrew King (Oxford) Ching Kung (University of Wisconsin) Nikos Logothetis (Max Planck) Markus Meister (Harvard) Cynthia F. Moss (University of Maryland) Hitoshi Sakano (University of Tokyo) Kristin Scott (UC Berkeley) Leslie Ungerleider (NIMH) Leslie Vosshall (Rockefeller) Stephen Waxman (Yale) Charles Zuker (Columbia) For more information and to register visit our site by clicking Apply Now below. http://www.newscientistjobs.com/jobs/job/formulation-scientist-225337-nj-new-jersey-200645875.htmFri, 20 Nov 2009 20:59:35 +0000196366A leader in therapeutic antibodies, ImClone Systems is committed to advancing oncology care by developing a portfolio of novel targeted biologic treatments designed to address the medical needs of patients with a variety of cancers. Founded 25 years ago, ImClone Systems has a rich culture of biotechnology innovation and leading-edge medical science. Our deep expertise in molecular biology, oncology, genomics and antibody engineering has helped us establish a robust pipeline of products that are in various stages of clinical development and span virtually all major solid tumor types. ESSENTIAL DUTIES AND RESPONSIBILITIES 1. Assists in the development of formulations for protein therapeutics. 2. Operation of analytical instrumentation including: HPLC, Electrophoresis (SDS-PAGE and IEF), Spectrophotometer, CD, Fluorimeter, DSC, FTIR, HIAC, DLS, pH meter, Conductivity Meter, Osmometer and Freeze Dryer. 3. Execute experiments, analyze data, and report results to supervisor within timelines. 4. Active participation with supervisor in planning and executing experiments. 5. Write SOP’s, study protocols and technical reports. 6. Sample management and monitoring of stability samples. 7. Assay development and trouble shooting. 8. Assist in the development of final drug dosage forms. 9. Maintain Laboratory and Laboratory Records. 10. Work in a safe manor compliant to ImClone Systems policies and procedures. ESSENTIAL KNOWLEDGE, SKILLS, EXPERIENCE 1. BS in Biochemistry/Pharmaceutical Science with 8-12 years of relevant industry experience or MS in Biochemistry/Pharmaceutical Science with 4-8 years of relevant industry experience. 2. Knowledge of the use of and experience with Spectrophotometer, CD, Fluorimeter, DSC and HPLC is preferable. 3. Must have good written and oral communication skills. 4. Must have good organization and documentation skills. 5. Must have the ability to accurately prepare solutions, perform experiments and analyze data. 6. Must be detail orientated and have demonstrated time management skills. To apply please visit http://www.imclone.com/careers_imclone.php,Requisition #225337. http://www.newscientistjobs.com/jobs/job/research-scientist-imclone-systems-110490-new-york-ny-ny-new-york-200641018.htmFri, 20 Nov 2009 20:54:25 +0000196364A leader in therapeutic antibodies, ImClone Systems is committed to advancing oncology care by developing a portfolio of novel targeted biologic treatments designed to address the medical needs of patients with a variety of cancers. Founded 25 years ago, ImClone Systems has a rich culture of biotechnology innovation and leading-edge medical science. Our deep expertise in molecular biology, oncology, genomics and antibody engineering has helped us establish a robust pipeline of products that are in various stages of clinical development and span virtually all major solid tumor types. ImClone Systems is recruiting for a skilled and experienced individual to join our team of drug discovery as a Research Scientist. The successful candidate will be a highly motivated team player with a commitment to quality, and attention to detail, strong problem solving skills, and the ability to work productively. ESSENTIAL DUTIES AND RESPONSIBILITIES 1. ELISA and in vitro assays that measure antigen-specific cellular immunity 2. In vitro cell binding, flow cytometry, and pharmacological assays 3. Lymphocyte isolation and culture 4. Hands-on experience in running animal experiments 5. Basic molecular biology knowledge ESSENTIAL KNOWLEDGE, SKILLS, EXPERIENCE 1. BS or MS degree with strong background in immunology and tumor biology. 2. 3+ years for BS and 2+ years for MS with hands-on laboratory research experience. 3. Tumor Immunology, Immunohistology and animal handling experience a must. 4. Working knowledge of cell culture, immunology and related assays. http://www.newscientistjobs.com/jobs/job/research-faculty-computational-and-systems-biology-ny-new-york-200645874.htmFri, 20 Nov 2009 20:25:10 +0000196361Research Faculty Computational and Systems Biology The Computational Biology Program (cbio.mskcc.org) at MSKCC (ski.edu) seeks innovative investigators for tenure-track positions at the Assistant, Associate, or Full Professor level. Pursue basic research, solve biological problems with major emphasis on computational methods, and build active bridges to experimental and clinical research. Actively participate in building out research programs at one of the best clinical-scientific institutions in the world. Work in MSKCC’s new Zuckerman Research Center, on Manhattan’s Upper East Side, in close proximity to Rockefeller University and the Cornell Weill Medical College. Train graduate students in the Gerstner Sloan-Kettering Graduate School (sloankettering.edu), the Weill Cornell Graduate School of Medical Sciences and in tri¬-institutional graduate programs. Areas of special interest include chemical biology, physiology, developmental biology, neurobiology, genetics and cancer biology. Applicants should have a doctoral-level degree and the potential to develop an independent, interdisciplinary research program. MSKCC offers a highly interactive, supportive and dynamic research environment with programs in Computational Biology, Developmental Biology, Molecular Pharmacology & Chemistry, Cancer Biology & Genetics, Structural Biology, Immunology, Cell Biology, Molecular Biology, and Human Oncology and Pathogenesis, as well as unparalleled clinical programs in cancer research, treatment and prevention. E-mail your application (PDF) by clicking Apply Now below as soon as possible in December 2009 but no later than January 10, 2010. Detailed instructions at cbio.mskcc.org/faculty-search/. Need more information? E-mail Dwana Agosto: agostod@mskcc.org Department Chair: Chris Sander. MSKCC is an affirmative action, equal opportunity employer. http://www.newscientistjobs.com/jobs/job/research-associate-iii-ca-california-200645870.htmFri, 20 Nov 2009 19:22:09 +0000196352My company shares my passion for helping to improve human health around the world.” “This is My MedImmune.” Those who join MedImmune feel a sense of ownership about their future. They thrive with a recognized leader in the biotechnology industry and the wholly-owned subsidiary of AstraZeneca plc. Here, you will join passionate professionals who advance science, technology and medicine to develop products designed to help people live better lives. You will excel in an environment characterized by respect, integrity and growth opportunities…that encourages both individual contribution and collaborative entrepreneurial thinking. Our products and/or product candidates are designed to address areas of need in infection, oncology, respiratory disease and inflammation, cardiovascular/gastrointestinal disease and neuroscience. Explore a MedImmune career as we strive to better more lives, more often, around the world. Title: Research Associate I/II Location: CA, Santa Clara - NON SALES Req: 02076 Major Duties and Responsibilities (including supervising others): Development and/or optimization of virus upstream processes (from cell thaw through viral harvest). This includes designing experiments, analyzing data, developing batch records, SOPs and protocols, and writing and/or reviewing technical reports. This may also include the evaluation of alternative methodologies and/or materials for various process operations and steps. Serve as a member of the team responsible for the technology transfer of processes to large scale manufacturing sites. This includes writing and/or review of batch records and contract manufacturing staff, and providing the necessary technical support to the contract manufacturer once the process has been transferred and cGMP manufacturing has begun. Maintenance of upstream process development equipment including bioreactors, cell counters, metabolite analyzers, pumps and gauges. Maintenance of inventory for commonly used lab supplies. Other responsibilities as required by the department or team. JOB REQUIREMENTS: Requirements/Qualifications: Education: B.S. in Engineering Experience: 2-5 years Special Skills/Abilities: Bioreactor operation Job Complexity: Cell culture in Biolevel 2 labs Supervision: Supervision required If you are interested in this position please click the Apply Now button below. Req #. 01889 MedImmune is an Equal Opportunity Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, veteran status, or any other characteristic protected by federal, state or local law. http://www.newscientistjobs.com/jobs/job/associate-scientist-iiscientist-i-md-maryland-200645868.htmFri, 20 Nov 2009 19:16:57 +0000196350My company shares my passion for helping to improve human health around the world.” “This is My MedImmune.” Those who join MedImmune feel a sense of ownership about their future. They thrive with a recognized leader in the biotechnology industry and the wholly-owned subsidiary of AstraZeneca plc. Here, you will join passionate professionals who advance science, technology and medicine to develop products designed to help people live better lives. You will excel in an environment characterized by respect, integrity and growth opportunities…that encourages both individual contribution and collaborative entrepreneurial thinking. Our products and/or product candidates are designed to address areas of need in infection, oncology, respiratory disease and inflammation, cardiovascular/gastrointestinal disease and neuroscience. Explore a MedImmune career as we strive to better more lives, more often, around the world. Title: Associate Scientist II/Scientist I Location: CA, Mountain View - NON SALES Req: 02056 Position Summary: Major Duties and Responsibilities (including supervising others): We are seeking a highly motivated independent individual to join our formulation team aimed at formulation development for biologics including protein and live viruses. The individual will be working with the team focusing on formulation studies and characterizations for liquid or solid dosage formulations. The essential responsibilities will include planning and executing pre-formulation and formulation studies, developing and performing biophysical, biochemical and biological analyses. An ability to work independently and have effective organization and communication skills is essential. Special Skills/Abilities: Expertise in pre-formulation and formulation of proteins and antibodies required. Hands on expertise in analytical techniques including HPLC-SEC, RP-HPLC, FTIR, fluorescence assays, DSC/mDSC are required. A prior experience in ajuvant formulation development is a plus. Experiences with solid state analyses such as Karl-Fischer, TGA, DVS, particle sizing desired. Excellent oral and written skills required. Job Complexity: Medium-High. JOB REQUIREMENTS: Supervision: Work is performed with minimal supervision. (supervision required, level of independence) Requirements/Qualifications: Education: Degree in Chemistry, Chemical Engineering, Pharmaceutical Sciences, Biochemistry, Biophysics. Experience: Ph.D. + 0-3 yrs, M.S. + 8-10 yrs, B.S. + 10-13 yrs. If you are interested in this position please click the Apply Now button below. Req #. 02005 MedImmune is an Equal Opportunity Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, veteran status, or any other characteristic protected by federal, state or local law. http://www.newscientistjobs.com/jobs/job/pre-clinical-project-leader-pre-clinical-project-director-pre-clinical-project-manager-switzerland-zurich-200645810.htmFri, 20 Nov 2009 17:38:12 +0000196251The oppportunity exists for a Pre-clinical Project Leader to develop their skills at one of Switzerland's top Biotechs. This role will involve: - Defining research and development plans - Planning and performing of experiments to identify drug candidates - Building and coordinating the scientific project team - Coordinating and supervising CROs With a profound knowledge of biochemistry and cell biology the ideal candidate will have over five years experience in working within oncology studies and supervising animal experience Please contact me for further details. At RBW Consulting Ltd, every one of our consultants has the benefit of five years experience in helping Pharmaceutical Professionals find the jobs they are looking for in the industry. With unrivalled industry knowledge and excellent links with hiring managers in Biotechs, Pharmas and CROs throughout the UK, Europe and across the world, we would be delighted to speak with you about the role you are looking for. Call +44 (0)1293 584 300 or email howard.johnson@rbwconsulting.com for a confidential discussion about your options for progression. Keywords: Pre-clinical Project Leader, Pre-clinical Project Director, Pre-clinical Project Manager, Clinical Research Associate, CRA, Clinical Research, Clinical Research Scientist, International Monitoring, Project Manager, Clinical Project Manager, Clinical Project Director, Director of Clinical Operations, Clinical Study Manager, Oncology, CNS, Junior Project Manager, Lead CRA, Pharma, Biotech, International, CRO http://www.newscientistjobs.com/jobs/job/experienced-data-manager-south-coast-clinical-research-slough-200645751.htmFri, 20 Nov 2009 17:06:13 +0000196137Experienced Data Manager - South Coast - Clinical Research An excellent opportunity has arisen for an experienced Clinical Data Manager to work in a Mid Sized Clinical Research Organisation in an outstanding rural location. As the senior clinical data manager (CDM), you will be expected to lead and coordinate all aspects of clinical trials data, working on phases I to IV studies. You will insure that all tasks are carried out efficiently according the clients specific budgets and deadlines, maintaining constant communication with the clients via telephone, email and video conferences. You will attend information and presentations on behalf of the clinical data management team, these will include workshops and project planning meetings as appropriate. Your technical duties will include identify errors and inconsistencies in CRF data and ensuring their resolution in order that databases can be declared clean and locked according to ICH GCP standards. In return you will receive a generous salary, competitive benefits package and an outstanding relocation package!!! For further information or to apply to this role, please contact Marie Tucker on 0121 616 3470 KEYWORDS: Clinical Data Manager, CDM, Senior, Clinical Research Organisation, Paramount Recruitment Limited provides services as an agency and an employment business. We regularly have similar roles in this area. Please see our website for details or send your CV in to us to find out the latest opportunities. http://www.newscientistjobs.com/jobs/job/statistician-clinical-buckinghamshire-sas-buckinghamshire-200645745.htmFri, 20 Nov 2009 17:03:51 +0000196128Statistician - Clinical - Buckinghamshire - SAS Experienced Clinical Statistician required in Buckinghamshire - A fantastic opportunity has arisen for an experienced Statistician to join a mid-sized Clinical Research Organisation (CRO) within their Buckinghamshire offices. Working alongside a team of high calibre senior biostatisticians, you will help provide statistical support for clinical studies including: study design, sample size calculations, patient randomization, statistical analyses, interpretation of data and reporting of results. In addition, you will help assist in the writing of statistical analysis plans and the design of statistical tables, figures, and data listings for clinical summary reports. The ideal candidate will be educated to a MSc level in statistics, biostatistics or related discipline. To succeed in this role it is essential that you have a strong SAS programming background with prior knowledge in applied parametric and nonparametric statistics. You should be confident in your ability to translate clients' needs into statistical practice and educate clients in the use of statistics. This opportunity is ideal for a biostatistician/clinical statistician with 2 years plus experience looking for that next step in their career. In return you will receive a generous salary, fantastic benefits package and much, much more! For more information on this role please call Kieron McDaid 0121 616 3462 Keywords: Biostatistics, statistician, clinical research organisation, pharmaceutical, CRO, SAS, R, Biostatistician. Paramount Recruitment Limited provides services as an agency and an employment business. We regularly have similar roles in this area. Please see our website for details or send your CV in to us to find out the latest opportunities. http://www.newscientistjobs.com/jobs/job/research-scientist-hertfordshire-200645742.htmFri, 20 Nov 2009 17:03:26 +0000196125Lab Support is recruiting Resarch Scientists within a small product development group of an exciting new biotechnology company. The role will be to develop a novel PCR-based medical device for the detection of live cells in clinical samples and will also encompass development of the device to improve sensitivity. MAIN DUTIES AND RESPONSIBILITIES • Sample preparation handling clinical samples, including bacterial and fungal cell culture. • Device development using PCR • Validation studies prior to launch. Minimum Requirements/Qualifications: • BSc/MSc/PHD or equivalent qualifications in a Biosciences subject is required. • Either microbiological or molecular (PCR) based laboratory experience essential. • Experience of working in NHS environment and familiarity with current microbiological testing in hospitals essential. • Experience of working to ISO 9001 and ISO13485 is hihgly desirable. The ideal candidate will be qualified to PhD level or equivalent with substantial microbiological or molecular (PCR) experience. NHS experience and knowledge of current microbiological testing in hospitals is essential. Please apply with full CV outlining your experience in this field and quoting ref CAM-LZG-2011. Please note that candidates without the relevant experience may not be contacted. To apply for this role please call 01223 451021 or email your CV to cambridge@labsupport.co.uk quoting reference number CAM-LZG-2011. Lab Support is unable to employ any candidates requiring a sponsorship to work in the UK and all applicants must be in a position to accept employment without infringement of their immigration status. Lab Support is working as an Employment Business in relation to this role. http://www.newscientistjobs.com/jobs/job/biostatistician-sas-programmer-paramount-clinical-research-berkshire-200645736.htmFri, 20 Nov 2009 17:00:53 +0000196121Biostatistician - SAS Programmer Paramount Clinical Research CRO A multicultural global Clinical Research Organisation is seeking a Clinical Database and SAS Programmer to join their expanding team in Berkshire As the Biostatistician or SAS Programmer you will be providing SAS programming and technical support to a range of projects, in accordance to client's allocated timelines and budgets. You will regularly be expected to communicate with the clinical data manager in regards to programming related issues and assist them with data reviews. Your technical duties will include designing and building clinical databases and performing database validations. Inputting data into CRF's, programming and validating electronic data checks will also be required. If successful, you will help carry out ad hoc programming tasks and maintain coding dictionaries. This opening will require you to review and update SOPs, mentor other members of the team when required and interact with external suppliers for the delivery of electronic data. The ideal candidate will be educated to at least BSc level in Statistics or similar discipline. You will have over twelve months SAS/ Database programming experience with in a pharmaceutical or clinical research organisation. An ability to work as part of a team alongside excellent interpersonal skills is essential for this post. In return you can expect to receive a generous salary and a competitive benefits package. This is a fantastic opportunity for career progression, within a continuously expanding biometrics team. For further details about this opportunity contact Kieron Mc Daid on +44(0)121 616 3462 Paramount Recruitment Limited provides services as an agency and an employment business. We regularly have similar roles in this area. Please see our website for details or send your CV in to us to find out the latest opportunities. http://www.newscientistjobs.com/jobs/job/validation-officer-kent-200645727.htmFri, 20 Nov 2009 16:54:15 +0000196080We are currently looking for a Validation Officer to join a leading Biotechnology company based in the Kent region. Purpose of the role To undertake various validation activities assigned by Validation Manager. Key Responsibilities To prepare, execute and report validation protocols Responsibilities include the validation of: * Equipment (Protocol Writing, Execution, Report Writing / Approval) * Production Processes (Protocol & Report Writing / Approval) * Analytical Methods (Protocol & Report Writing / Approval) * Facilities and Utilities (Protocol & Report Writing / Approval) * Computer Systems (Protocol & Report Writing / Approval) * Cleaning Studies (Protocol & Report Writing / Approval) * Shipping Studies (Protocol & Report Review/ Approval) Establish and maintain the re-qualification schedule for validated equipment. To perform temperature mapping of refrigerators, freezers and incubators. Liaise with Engineering, Quality Assurance and User Departments to ensure that validation is conducted in a timely manner with minimal disruption to production. Ensure that the necessary documentation in place and current to control all aspects of validation. Review of Manufacturing Procedures to ensure that appropriate validation work has been completed prior to approval of the procedure. Co-ordinate validation documentation systems in conjunction with QA. Attend meetings, both internal and external, representing the department in a professional manner. Participate in audits by customers and regulatory authorities. To ensure that safe working methods and practices are adopted at all times and in accordance with Company policy for the safety of the postholder and others within the working environment. To be responsible for housekeeping, tidiness and general cleanliness of all areas in which the post holder is working. To assist in training of other staff as required. Scope/Impact Works independently under general supervision and direction. Work is reviewed for soundness of judgment and overall adequacy and accuracy. Performs work that consistently requires independent decision making and the exercise of independent judgment and discretion. It is important that the post holder is self motivated and can manage multiple tasks. Knowledge, skills and experience required Degree level, preferably in Chemistry, Biology, Engineering or a Related Subject Understanding of ISO 9000 Quality System Knowledge of cGMP General understanding of IQ, OQ, PQ, PV. Temperature mapping. Understanding of Cleaning validation. Ability to author and execute validation reports. Ability to write validation related procedures. Understanding of calibration principles. Use of Microsoft Word, PowerPoint and Excel. To apply for this position, candidates must be eligible to live and work in the UK Matchtech Group Plc is acting as an Employment Agency in relation to this vacancy. http://www.newscientistjobs.com/jobs/job/senior-project-manager-reading-clinical-research-berkshire-200645726.htmFri, 20 Nov 2009 16:53:41 +0000196079Senior Project Manager - Reading - Clinical Research Due to expansion a fantastic opportunity has arisen for a Senior Project Manager within a global pharmaceutical organisation based in Reading. This particular division provides pharmaceuticals with pioneering computerised evidence-based services and solutions used throughout the drug development process, from first-man trials to large worldwide phase IV trials. As Senior Project Manager you will be responsible for managing and developing training events and service projects for clients. Your duties will include: * Managing several projects at a time * Managing more junior members of the project team * Identifying new opportunities * Building and managing client relationships * Assisting with the development of new clients This position would be ideal for candidates with a degree in a business related subject, with around seven years professional business experience. You will need to have previous project staff management and project management experience. Entrepreneurial spirit is a must. This is an opportunity to become part of a forward thinking culture where high performance is rewarded. There are extensive training and progression opportunities, giving you the chance to move up the career ladder. They also offer a host of other benefits including healthcare, bonus scheme and life assurance. For more information on the role and company please call Marie Tucker on 0121 616 3470 Keywords: Project Manager, Project Management, Clinical Research, Clinical Trials, Reading, Berkshire, Project Specialist, CRA, Senior Project Manager, Lead Project Manager Paramount Recruitment Limited provides services as an agency and an employment business. We regularly have similar roles in this area. Please see our website for details or send your CV in to us to find out the latest opportunities. http://www.newscientistjobs.com/jobs/job/national-sales-manager-sales-director-designate-it-sales-manager-united-kingdom-200645724.htmFri, 20 Nov 2009 16:53:26 +0000196077National Sales Manager – Sales Director Designate – IT Sales Manager Zest Medical is currently working in partnership with a leading provider of medical transcription, digital dictation and speech recognition services in order to recruit a highly accomplished IT Sales Manager to lead a national team of sales specialists. My clients bespoke technology and services have been designed specifically for the medical sector; delivering solutions to NHS Trusts, GP practices and private medical groups. Widely recognised within the industry for providing excellent value at all levels, exceeding the expectations of clinicians, administrators and management, my client is well positioned to execute an aggressive growth strategy. This role provides an excellent platform for a talented, ambitious IT Sales Manager to demonstrate their value, with clear career pathway into the Sales Director role. The IT Sales Manager will play an integral role in developing, maintaining and implementing a UK sales strategy to support business positioning. Incorporating product and key account plans linked to strategic company goals, incorporating the plan into sales team objectives and goal setting. The IT Sales Manager will continually measure personal and team successes against the national sales plan, implementing the necessary challenges, interventions and decisions to successfully deliver or exceed plan expectations. The management and development of the abilities and successes of the sales team is fundamental to the post. The IT Sales Manager will provide role model leadership and management activity including coaching, goal setting and effective delegation to stretch and develop team competencies. Through regular observation, appraisal and monitoring you will encourage and identify excellent performance, additionally, intervene where performance or compliance is below expectation. The ideal candidate will be educated to degree level (minimum) with a proven track record, successfully managing IT Sales teams. Strong leadership skills are essential coupled with polished presentation / communication skills. The role requires hands on leadership with the capacity to drive change, motivating and encouraging in order to develop a culture of excellence within the organisation. A good working knowledge of the principles and methodology of the National Programme for IT (NPfIT) is advantageous; however, not essential as my client is receptive to reviewing candidates from other complex sectors. The successful candidate will be rewarded with a highly competitive remuneration package with a basic salary ranging from £60,000 - £80,000 (DOE) + Uncapped Bonus (100% Target/£125,000) and a range of additional benefits. In order to discuss this opportunity in greater depth contact Zest Medical today on 0114 2381724 or alternatively forward an updated version of your CV to matthew.morland@zestmedical.com