http://www.newscientistjobs.com/jobsNew Scientist Jobshttp://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/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/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/postdoctoral-positions-with-interest-in-protein-structure-function-high-ca-california-200633780.htmFri, 20 Nov 2009 16:29:31 +0000195920Postdoctoral position(s) are immediately available for candidates with interest in protein structure-function, high density lipoproteins (HDL), or lipid metabolism. The focus of our group is on HDL, namely HDL metabolism and the structure -function of HDL's main protein component, apolipoprotein A-I. We are leaders in the field of apolipoprotein structure-function, utilizing this understanding to describe the role of HDL in the prevention of atherosclerosis and towards the improvement of hydrophobic drug delivery. Projects include examination of cellular and physiological processes that govern HDL biogenesis, characterization of genes involved in HDL formation and cholesterol mobilization, analysis of apolipoprotein structure, functional analysis of structural features of apolipoproteins, and investigation into the effect of incorporation of hydrophobic drugs onto HDL. Experience in cell biology, protein chemistry and/or lipid metabolism is encouraged. Position qualifications: The candidate should have completed a PhD, MD or PhD/MD and be available to relocate to the SF Bay Area. Emphasis will be placed on candidates with a background in protein chemistry, genetic analysis, RNA knockdown, o fluorescence microscopy. Furthermore, those with history of team-work and group coordination will be prioritized. PHYSICAL REQUIREMENTS: Sit: Up to 8 hours/day Stand/Walk: Up to 6 hours/day Bend/Stoop: Up to 6 hours/day Reach: Up to 6 hours Rep Use of UE/Grasp: Up to 8 hrs Lift/Push/Pull: 25lbs, over 25# with assistance or equipment This job requires the ability to hear alarms clients and/or instruction. The ability to see accurately from 20 inches to 20-ft. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential function of this position. TO APPLY CLICK APPLY NOW BELOW AND REFERENCE POSITION 5262 http://www.newscientistjobs.com/jobs/job/postdoctoral-positions-in-immunobiology-ca-california-200633781.htmFri, 20 Nov 2009 16:29:14 +0000195921This is a position in a immunobiology laboratory performing basic and pre-clinical research related to vaccines against disease caused by bacterium Neisseria meningitidis. Duties will include performing various immunobiological assays, including assays involving live N. meningitidis organisms, processing of human blood samples, and potentially animal work. BACKGROUND AND ACCOMPLISHMENTS: the successful candidate will have a theoretical and practical understanding of molecular biology and microbiology. A Ph.D. in microbiology. molecular biology, or a related field is essential. Previous experience with transcriptional profiling by quantitative RT-PCR and/or microarrays, gene cloning, protein expression, purification and characterization is preferred. Attention to detail and strong organizational and communication skills are required. INTERPERSONAL SKILLS AND MANAGEMENT SKILLS/GOALS: 1. Promotes a constructive and positive atmosphere within the work area by cooperating with and assisting investigators and other staff. 2. Is an effective problem solver through active problem identification and collaboration with investigators and other staff. Interacts with others in a courteous, professional manner with appropriate confidentiality. 3. Uses appropriate organizational skills in setting priorities for work and meeting deadlines. 4. Is able to resolve conflicts in a pro-active manner that demonstrates a high level of understanding of and interest in conflict resolution. 5. Contributes to Institutional affairs as appropriate.Postdoctoral Fellow 0-3 years experience; Ph.D. or MD Learns new and/or advanced research skills and techniques. Participates in design of experiments and interpretation of results. Originates publication and presentation of data from laboratory. May seek and obtain external grant funding Senior Postdoctoral Fellow 3+ years experience; Ph.D. or MD In addition to Postdoctoral Fellow responsibilities, may supervise staff member(s). May obtain grant or fellowship funding. Shows potential for independent research through continued publications and presentations PHYSICAL REQUIREMENTS: Sit: Up to 8 hours/day Stand/Walk: Up to 6 hours/day Bend/Stoop: Up to 6 hours/day Reach: Up to 6 hours Rep Use of UE/Grasp: Up to 8 hrs Lift/Push/Pull: 25lbs, over 25# with assistance or equipment This job requires the ability to hear alarms clients and/or instruction. The ability to see accurately from 20 inches to 20-ft. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential function of this position. TO APPLY CLICK APPLY NOW BELOW AND REFERENCE POSITION 5206 http://www.newscientistjobs.com/jobs/job/assistant-associate-or-full-professor-new-york-ny-new-york-200644071.htmFri, 20 Nov 2009 15:15:42 +0000195485A position is available at the SUNY Downstate Medical Center to develop a cutting-edge research program in proteomics, lipidomics and metabolomics. The appointment will be made on the level of assistant, associate or full professor depending on experience, publications and past and current extramural funding. In addition to developing an independent and extramurally funded research program, the successful individual will be expected to direct a newly established, institutional proteomic core facility that has a strong focus on biomarker discovery of translational significance. The successful candidate will be responsible for developing and implementing protocols and data processing for our existing LC/MS/MS and MALDI technologies. Preference will be given to applicants with demonstrated interest in and ability to participate in a wide spectrum of multi-disciplinary research in a collaborative setting. Expertise in FACS analyses and ongoing extramural research support will be considered advantageous, but is not a requirement. Please submit your C.V. and letters of recommendation to: Alan Gintzler, Ph.D., SUNY Downstate Medical Center. Full mailing address can be found by clicking View Contact Details. Or apply via email by clicking Apply Now. http://www.newscientistjobs.com/jobs/job/manager-project-management-tx-texas-200644512.htmFri, 20 Nov 2009 14:43:15 +0000195384The statements below reflect the general responsibilities and requirements of the identified position but may not describe all the work requirements that may be inherent in the job. It is the responsibility of each employee to comply with all applicable regulations e.g. Good Clinical Practice, Good Manufacturing Practice, Good Laboratory Practice in the performance of their role. Job Summary: Responsible for management, administration, and organization of the Project Management department. The group provides Clinical Study Management of Phase I Clinical Trials. Position is responsible for ensuring efficient utilization of all resources, both human and physical. Duties and Responsibilities: . Responsible for Clinical Operation's Project Management team, including coordination and study management staff. . Ensure all work is carried out in strict accordance with the relevant protocols, Standard Operating Procedures, and in compliance with Good Clinical Practices. . Meet the scientific and medical standards laid down by the Scientific and Medical Directors. . Ensure that the safety, welfare and dignity of volunteers are not compromised. . Ensure that the highest levels of client service are maintained. . Assist Client Services in developing client proposals and attend client meetings as needed. . Assist Client Services with client visits and interactions as appropriate. . Initiates collaborative relationships with other Covance Business Units when required. . Initiates procurement of external resources, consultants, or equipment when protocol required. . Develops strategies for efficient study conduct, data collection, subject management, and safety monitoring. Coordinates efforts interdepartmentally to accomplish these strategies. . Assumes role of Study Manager or co-manager when necessary. . Ensure that appropriate training and career development takes place so that staff can adequately perform their duties to the forecasted workload and develop to their fullest career potential. . Keeps up to date on current developments in all aspects of his/her job and initiate improvements where and when appropriate. . Responsible for compliance with all applicable regulations relating to the conduct of clinical trials. . Continuously seeks out new and better ideas, driving best practices and benchmarking externally. . Performs other related duties as assigned. Principal Contacts . Internal: Any level of individual across the business units and throughout the Covance organization. . External: Interacts routinely with Study volunteers, clients, vendors, and peers in the industry. Travel Requirements: . Yes, occasional travel Language Skills Required: . Speaking: Yes, English . Writing/Reading: Yes, English Working Conditions: . Mandatory immunizations and screening as required. . Handling of biologically hazardous and radiolabeled material is necessary. . Must be able to see (distinguish colors) and hear to meet, if necessary, the job requirements. . Must have excellent command of the English language, both oral and written. . Must be able to use hands to finger, handle, or touch objects, tools or controls, including a computer keyboard, for up to 6 hours per day. . Must be able to stand and/or bend for up to 6 hours per day. . Must be able to distinguish colors. Special Factors: . Overtime and weekend work as required. Education/Qualifications Required: . Bachelor of Science (BS) in medical or science or related field. Experience Required: . 6-8 years clinical research or related experience. . 4-5 years of progressive and proven leadership responsibilities in clinical research project management. . Six Sigma Green Belt is preferred. . Additional experience may be substituted for education requirements. Start time 07:30 Days per week Mon - Fri (weekends as necessary) http://www.newscientistjobs.com/jobs/job/faculty-positions-cancer-biology-fl-florida-200645280.htmFri, 20 Nov 2009 13:34:56 +0000195084The Donald A. Adam Comprehensive Melanoma Research Center at the Moffitt Cancer Center is seeking laboratory-based faculty members with a Ph.D., M.D. or M.D.-Ph.D. with an interest in melanoma research. The prospective candidates will be appointed at the Assistant, Associate or Senior Member level, and it is expected that they would establish an independent funded laboratory research program concentrating on translational investigation in the fields of cancer stem cells, angiogenesis, metastasis, tumor microenvironment, apoptosis or the cell cycle. While candidates working on any cancer type will be considered, preference will be given to those with an interest in melanoma research. An outstanding start-up package is available, as well as a highly competitive salary and excellent lab space. A specific attraction is the opportunity to interact with ongoing well-funded research programs in molecular oncology, drug discovery, population science and translational immunology/immunotherapy. The Comprehensive Melanoma Research Center brings together clinicians, basic and translational scientists at Moffitt to aggressively pursue new ideas in the etiology, treatment and prevention of melanoma. The Moffitt Research Institute is comprised of approximately 140 Principal Investigators, 58 laboratories, and 306,000 square feet of research space. Outstanding Core Facilities are available to the investigators. The Cancer Center is comprised of a large ambulatory care facility, a 206-bed hospital, with a 36-bed blood and marrow transplant program, 12 state of the art operating suites, a 30 bed intensive care unit, a high volume screening program, and a basic science research facility. The Moffitt Cancer Center is affiliated with the University of South Florida. Primary and secondary University appointments are available, as applicable. Academic rank is commensurate with qualifications and experience. For inquiries about the position, contact Dr. Srikumar Chellappan at 813-745-6892 or Dr. Jeffrey Weber, Director, Donald A. Adam Comprehensive Melanoma Research Center, at 813-745-2007. Moffitt Cancer Center provides a tobacco-free work environment. It is an equal opportunity, affirmative action employer and a drug free workplace. http://www.newscientistjobs.com/jobs/job/associate-director-study-management-bioanalytical-wi-wisconsin-200644649.htmFri, 20 Nov 2009 09:31:51 +0000194060Imagine working in one of the most exciting and professionally satisfying industries anywhere. Imagine being involved in cutting-edge projects on a daily basis. At Covance, your imagination, your dedication, and your drive to find solutions to challenging projects begin on your very first day. Covance is one of the world's largest and most respected contract research organizations. Our clients are a Who's Who of the pharmaceutical and biotechnology industry. If you're looking for a diverse and stimulating work environment, you'll find it at Covance. It is a great time to join Covance! Covance is currently looking for an Associate Director in our global Bioanalytical Services organization. This role is located in Madison, WI and has responsibility for the Principal Investigation team at our Madison WI and Indianapolis IN bioanalytical locations. The Associate Director is responsible for: . Directing a staff responsible for the scientific conduct of bioanalytical projects. . Assure scientific quality and client service targets are achieved. . Consult with clients on studies placed with the Bioanalytical Services Department. . Develop and execute a strategic plan, in consultation with the Director, which identifies the areas in which the department will concentrate its Study Management efforts. . Initiate, plan and implement staff development programs within the Study Management group. Develop capabilities and resources to meet both present and future needs within this group. Education/Qualifications . Ph.D. in Analytical Chemistry or related field and 8 years of experience. . Experience may be substituted for education. Experience . Prior experience in a Bioanalytical field is preferred. . Prior experience working in a regulatory environment is needed. . Skilled in performing presentations. . Skilled time management, planning and budgeting. . Experienced in leading and developing people. Covance offers extraordinary career opportunities to our employees. Here you will find a place to learn, grow, and achieve . a place to call your professional home. We provide the opportunity for a career with purpose in an environment that values achievement and supports a balance between personal and professional lives. We invite you to join us at Covance and to work with us in bringing hope to millions of patients around the world. We believe this decision may be the most rewarding career move you will ever make. Covance is committed to diversity in the workplace and is an equal opportunity employer. (M/F/D/V). Your confidentiality and privacy are important to us. http://www.newscientistjobs.com/jobs/job/sample-management-supervisor-in-indiana-200644646.htmFri, 20 Nov 2009 09:30:41 +0000194022To supervise the activities of operational staff responsible for sample management of biological samples. Responsible for data review and data management. All activities are conducted in compliance with appropriate SOPs and regulatory agency guidelines. Education/Qualifications . BS/BA degree in Science, or equivalent degree plus 3-4 years related experience. Experience may be substituted for education. . Knowledge of appropriate regulatory agency guidelines. . Working knowledge of laboratory operations and an understanding of the technical aspects of the laboratory and/or computers and computer software systems. . Demonstrates strong organizational and communication skills. Start time 8 AM End time 5 PM Days per week 5 http://www.newscientistjobs.com/jobs/job/research-technician-tx-texas-200644504.htmFri, 20 Nov 2009 09:00:36 +0000193820The postion of a study tech 1 includes: *Performing practical/administrative actitives of clinical trials. * Maintain protocol and regulatory requirements in Clinical Pharmacology. *Perform basic study procedures such as ECG's, and Vital Signs. Education/Qualifications *Must have a High School Diploma. *Must have 1-2 years of phlebotomy experience. Experience Highly desirable candidates will have 1-2 years of experience in a doctors office. http://www.newscientistjobs.com/jobs/job/professional-healthcare-representative-york-pa-pa-pennsylvania-200643882.htmThu, 19 Nov 2009 12:27:29 +0000192293The Professional Healthcare Representative may have a variety of roles, such as the responsibility for sales targets and physician relationships within a specific geography. The Professional Healthcare Representative must demonstrate a strong understanding of necessary disease states and possess a solid ability to communicate necessary technical, scientific, and product and disease management information to customers. The Professional Healthcare Representative will provide the most current information pertaining to Pfizer products and their approved indications in a manner which will ensure the appropriate use of these products and achieve the business potential of the territory. Qualifications: • Bachelors Degree • Demonstrated business acumen • Proficiency using sales data/call reporting software/applications • Outside sales experience preferred Functional / Technical Skills can include: • Promotes broad portfolio of products (up to 9 total); Strong knowledge of disease states, therapeutic areas, and products • Drives sales in assigned accounts/with assigned physician targets • Cultivates relationships with KOLs; build lasting relationships with priority doctors • Assesses needs of target physicians; Addresses needs with responsive approach, targeted skills, and appropriate resources • Develops superior selling, technical and relationship building skills • Executes priorities of District Business Manager Throughout our 153 years, a legacy of caring for others has been at the heart of everything we do at Pfizer. This commitment is no less important when it comes to our employees. Pfizer wants to ensure that employees have resources to help them develop and succeed both in their careers and personal lives. One way we can achieve this is through our comprehensive benefits program, which offers employees and their eligible dependents the variety and flexibility to help address their needs at different stages in life. Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must have authorization to work for Pfizer in the U.S. In certain circumstances it may be advantageous to Pfizer to support the application(s) for temporary visa classification and/or sponsor applications for permanent residence so that a foreign national colleague can accept or remain in a work assignment in the U. S. For certain classes of temporary visas, the resulting work authorization may be specific to Pfizer and the specific job and/or work site. Pfizer may at its business discretion decide to or refrain from obtaining, maintaining and/or extending the temporary visa status and/or sponsoring a colleague for permanent residence and /or employment eligibility, considering factors such as availability of qualified U.S. workers and the colleague's long-term prospects for securing lawful permanent residence, among other reasons. Employment applicants requiring immigration sponsorship must disclose, when initial application for employment is made, whether or not they are legally authorized to work for Pfizer in the U.S. and, if so, whether that authorization permits them to work in the job they seek. In no case should Pfizer's support of a colleague's temporary visa application or sponsorship of a colleague for permanent residence be construed to guarantee success of that application or amend or otherwise invalidate the "at-will" employment relationship between the colleague and Pfizer. HOW TO APPLY: Please copy and paste the following URL into your browser address bar: http://posttrak.arbita.net/cgi-bin/PostTrak.cgi?RefCode=R6442125807948 http://www.newscientistjobs.com/jobs/job/become-a-biology-teacher-in-new-york-city-ny-new-york-200642973.htmThu, 19 Nov 2009 09:42:03 +0000191679The New Visions-Hunter College Urban Teacher Residency is a 14 month teacher-training program that fully integrates the graduate coursework of the aspiring teacher (resident) with intensive, hands-on experiences in New York City schools. Within a strong public school, residents collaborate one-on-one with an expert mentor teacher around all aspects of teaching. At the same time, residents take graduate courses at Hunter College specifically designed to align with experiences in urban schools. Residents are awarded a stipend of $22,500 plus health benefits during their residency year. Successful completion of the program results in a master’s degree in education and certification to teach in New York City. Graduates of UTR are hired within New Visions’ network of 76 public schools and are asked to commit to four years of teaching in New Visions schools after their residencies. For the 2010-2011 residency, UTR will be preparing 48 residents in English, biology, mathematics and special education for grades 7-12. For more information about the program, information sessions, and how to apply, please click Apply Now. http://www.newscientistjobs.com/jobs/job/postdoctoral-fellow-tufts-medical-center-boston-ma-united-states-200642985.htmWed, 18 Nov 2009 18:57:12 +0000190088NIH-funded position available in vascular biology, investigating the role of innate immunity in atheroclerosis. Ph.D in physiology, cell biology, immunology or related field required. Applicant must be a U.S. resident. The successful applicant will: • Conduct research on the role of Toll-like receptors and vascular progenitor cells in arterial disease. • Analyze data and prepare manuscripts for publication. • Assist in preparing and writing grant applications. Skills required: • Proficiency in general laboratory techniques including cell culture, use of transgenic mice, Western Blot analysis, PCR, and ELISA. • Experience in confocal microscopy or flow cytometry are desirable. • Ability to develop new techniques. • 1-2 years experience desirable. Please send CV and a statement of research interests by clicking Apply Now below Debbie Beasley, Ph.D. Associate Professor of Medicine Molecular Cardiology Research Institute Tufts Medical Center http://www.newscientistjobs.com/jobs/job/sallie-rosen-kaplan-fellowship-for-women-in-basic-clinical-epidemiological-or-prevention-science-md-maryland-200564268.htmWed, 18 Nov 2009 18:12:48 +0000190076Sallie Rosen Kaplan Fellowship for Women in Basic, Clinical, Epidemiological or Prevention science National Cancer Institute Sallie Rosen Kaplan Fellowship for Women in Basic, Clinical, Epidemiological Or Prevention Science The Sallie Rosen Kaplan Fellowship for Women Scientists in Cancer Research is made possible by a generous bequest to the Foundation for NIH (FNIH). This is a competitive program for female postdoctoral fellows applying to train in any of the National Cancer Institute’s intramural research settings, including basic, clinical, epidemiological, and prevention science. The postdoctoral fellowship experience at the NCI can serve as a first postdoctoral training assignment, or offer more experienced postdoctoral scientists an opportunity to further their training in more advanced methods, to acquire new research capabilities, to make changes in the direction of their research, or to receive training in fundamental sciences and clinical disciplines for the purpose of enhancing the transfer of biotechnology to cancer clinical programs. Program duration is normally 2 to 5 years. Fellows will be supported by a Cancer Research Training Award (CRTA), with an augmented stipend in the first year provided by the FNIH. The CRTA Fellowship stipend range is $44,600 to $82,400 commensurate with level of experience. Standard self and family health insurance is provided and high option coverage is available. Candidates for the Sallie Rosen Kaplan Fellowship must be female, must possess a doctoral degree, and must have less than 5 years postdoctoral research experience. U.S. citizenship or U.S. permanent residency (green card) is required. Finalists for the Kaplan fellowship will be notified by March 2010 and winners announced by May 2010. To be eligible for the Sallie Rosen Kaplan Fellowship award, the starting date of any NCI fellowship must be no earlier than December 14, 2009. Applicants are required to apply online at http://www.training.nih.gov/apps/publicForms/postdoctoral/forms/adIndex.aspx by December 11, 2009. Additional information about the Kaplan Fellowship can be found at http://www.cancer.gov/researchandfunding/training/srk DHHS, NIH and NCI are Equal Opportunity Employers http://www.newscientistjobs.com/jobs/job/research-associate-cincinnati-oh-academic-oh-ohio-200580542.htmWed, 18 Nov 2009 15:44:27 +0000189822A Research Associate position is available immediately in the Department of Cancer and Cell Biology at the University of Cincinnati Genome Research Institute. The candidate selected for this position will examine therapeutic targeting of the mTOR pathway in a mouse model in which c-myc and E2F1 transgenes are expressed in the liver. Cohorts of c-myc/E2F1 mice will be treated either with RAD001, BEZ235, the two both drugs in combination or novel mTOR kinase competitive ATP inhibitors. Sera and tissue extracts will be analyzed by Western-immunoblotting for signaling pathway activation, proliferation and apoptosis. The concentrations of RAD001 or BEZ235 in serum and in tissues will be measured by high-performance liquid chromatography/mass spectrometry (HPLC/MS/MS) to determine whether mTOR kinase competitive ATP inhibitors are more efficacious as single agents in the treatment of hepatocellular carcinoma than BEZ235 alone or in combination with RAD001. All qualified candidates should submit a CV to position number 29UC5115 via the UC jobs website by clicking Apply Now below.