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 +0000200311Clinical 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 +0000197477The 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 +0000197471Senior 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/pre-clinical-project-leader-pre-clinical-project-director-pre-clinical-project-manager-switzerland-zurich-200645810.htmFri, 20 Nov 2009 17:38:12 +0000197324The 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 +0000197210Experienced 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 +0000197201Statistician - 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/biostatistician-sas-programmer-paramount-clinical-research-berkshire-200645736.htmFri, 20 Nov 2009 17:00:53 +0000197194Biostatistician - 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/senior-project-manager-reading-clinical-research-berkshire-200645726.htmFri, 20 Nov 2009 16:53:41 +0000197152Senior 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/clinical-research-clinical-research-associate-jobs-portugal-unspecified-200645493.htmFri, 20 Nov 2009 16:29:31 +0000196984Flame Pharma Clinical Research Jobs - Clinical Research Associate Job - Portugal Flame Pharma are currently working alongside global expert Clinical Research Organisation in recruiting a Clinical Research Associate to be based in their innovative, state of the art facilities in Portugal. With over twenty year’s experience, this world class, therapeutically focused company are leaders in Cardiovascular Drug Development. If you are keen to progress within the field of clinical research this company will offer continuous training in order for you to realise your career goals. The Role: As a Clinical Research Associate the successful candidate will be responsible for site qualification, initiation, interim monitoring, site management and study close out visits for studies in accordance with Good Clinical Practices (GCP’s), local and international regulations and Standard Operating Procedures (SOP’s) In addition, you will ensure the quality of data submitted from study sites and assure a timely submission of data. The Person: Candidates must be qualified to degree level in a relevant discipline, combined with proven previous experience working as a CRA. Basic knowledge of three to five therapeutic areas including cardiovascular is required, as is a thorough understanding of standard operating procedures. Excellent interpersonal skills are also expected in communicating both internally within project teams, and also in liaising with clients externally. Candidates must be able to demonstrate a flexible attitude in their approach to the role as travel may be required. Fluency in both English and Portuguese are also essential. A competitive salary is on offer adjusted according to your qualifications and experience. For more information please contact Flame Pharma on 0800 085 0858 or email careers@flamepharma.com . http://www.newscientistjobs.com/jobs/job/clinical-research-associate-cra-home-based-clinical-research-united-kingdom-200645604.htmFri, 20 Nov 2009 16:06:45 +0000196864Clinical Research Associate ( CRA) - Home Based - Clinical Research A large, growing global Clinical Research Organisation (CRO) currently has opportunity available for a talented Clinical Research Associate (CRA) to be based from home. As a CRA you will be working on studies from phases II- IV. You will be responsible for: * Adhering to SOP's, ICH-GCP and other local regulations. * Assisting the project manager * Contributing to documentation design. * Performing initiation visits. * Performing monitoring visits. * Mentoring less experienced Clinical Research Associates. * Collecting data. Ideal candidates will be experienced in all phases of clinical trials and have a science related degree. You will need to have the ability to work well under pressure and to tight deadlines. In return the company offers continuous career development and training with every employee being assigned a mentor. The company have won a host of industry awards across the world and are continuing to grow year on year. Don't miss out on this opportunity to join a global service provider! For more information on the role and company please call Marie Tucker on 0121 616 3470 Keywords: CRA, Clinical Research Associate, Home based, home working, London, Wales, Scotland, England, UK, Birmingham, Manchester, CRO 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-associate-cra-hampshire-clinical-research-hampshire-200645558.htmFri, 20 Nov 2009 15:59:08 +0000196785Clinical Research Associate ( CRA) - Hampshire - Clinical Research A growing global Clinical Research Organisation (CRO) based in Hampshire currently has opportunity available for a talented Clinical Research Associate (CRA). As a CRA you will be working on studies from phases II- IV. You will be responsible for: * Adhering to SOP's, ICH-GCP and other local regulations. * Assisting the project manager * Contributing to documentation design. * Performing initiation visits. * Performing monitoring visits. * Mentoring less experienced Clinical Research Associates. * Collecting data. Ideal candidates will be experienced in all phases of clinical trials and have a science related degree. You will need to have the ability to work well under pressure and to tight deadlines. In return the company offers continuous career development and training with every employee being assigned a mentor, the opportunity to transfer to offices worldwide and long service awards. The company have won a host of industry awards across the world and are continuing to grow year on year. Don't miss out on this opportunity to join a global service provider! For more information on the role and company please call Marie Tucker on 0121 616 3470 Keywords: CRA, Clinical Research Associate, Hampshire, Southampton, Winchester, Eastleigh 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/publishing-manager-buckinghamshire-permanent-35000-45000-south-east-200645497.htmFri, 20 Nov 2009 15:50:18 +0000196693Publishing Manager, Buckinghamshire, Permanent £35,000-£45,000 My client is currently recruiting for a Publishing Manager to join their Global Publishing team, based in Buckinghamshire. This role will provide effective management and coordination for all publishing work undertaken. Main Responsibilities include: * Provide guidance to ensure documentation is complete, accurate, of high quality and electronically functional * Provide document advice and support for regulatory authority submissions and electronic publishing requirements * Identify potential submission problem areas * Develop new document and publishing process solutions * Oversee and perform specialized global publishing work Required Experience and Qualifications: * Degree Qualified * Good knowledge of Documentum and Coredossier * Excellent knowledge of submission guidance documents and regulations If this role is of interest please contact Vicky on 01189 594 990 or email vmara@clinicalprofessionals.co.uk Key Words: Publishing Documentation Document Submission Regulatory Affairs Documentum Core Dossier Buckinghamshire Berkshire Oxfordshire Relocatable http://www.newscientistjobs.com/jobs/job/cra-clinical-research-associate-buckinghamshire-clinical-buckinghamshire-200645454.htmFri, 20 Nov 2009 15:30:05 +0000196621CRA (Clinical Research Associate) - Buckinghamshire - Clinical Research One of the most impressive and highly desirable Clinical Research Organisations (CRO) to work for has an opportunity available for a talented Clinical Research Associate (CRA). As a CRA you will be working on studies from phases II- IV. You will be responsible for: * Adhering to SOP's, ICH-GCP and other local regulations. * Assisting the project manager * Contributing to documentation design. * Performing initiation visits. * Performing monitoring visits. * Mentoring less experienced Clinical Research Associates. * Collecting data. Ideal candidates will be experienced in all phases of clinical trials and have a science related degree. You will need to have the ability to work well under pressure and to tight deadlines. In return the company offers continuous career development and training with every employee being assigned a mentor, the opportunity to transfer to offices worldwide and long service awards. The company have won a host of industry awards across the world and are continuing to grow year on year. Don't miss out on this opportunity to join a global service provider! For more information on the role and company please call Marie Tucker on 0121 616 3470 Keywords: CRA, Clinical Research Associate, Buckinghamshire, High Wycombe, Reading, Maidenhead, Slough, 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/contract-regulatory-affairs-12-months-maternity-cover-berkshire-200645448.htmFri, 20 Nov 2009 15:27:49 +0000196612My client, a leading Biotechnology company situated in Berkshire are seeking a Regulatory Affairs Manager for a period of 12 months. This maternity cover requires candidates to work 22.5 hours per week, on site. The Regulatory Affairs Manager will join my clients team for 12 months (maternity cover) on a part-time basis (22.5hrs approx), to manage the regulatory requirements for our early stage clinical trials and oversee the MAA for our licensed product. Based at their corporate headquarters in Berkshire, you will be responsible for the preparation, submission and maintenance of INDs and Canadian and European CTAs and work closely with Clinical Project and Quality teams to ensure all regulatory requirements are met. You'll lead a small team and manage all regulatory timelines, budgets and external consultants as well as provide expert advice on legislative procedures when required. You will hold a life science degree and have considerable work experience in Regulatory Affairs and dealing with early stage clinical trials in the EU & US, preferably within small to mid-size Pharma. A pro-active and clear-thinking team player, you'll be used to working in a multi-disciplinary environment and have the strong interpersonal skills and adaptability needed to deal with tight deadlines and changing priorities Please note that this role requires applicants to work on site during the 22.5 hours. If you feel you have the credentials for this position, please submit your CV accordingly. (Keywords: Regulatory Affairs, Freelance Regulatory Affairs, Contract Regulatory Affairs, Clinical Trials, Sumbissions, Contract Regulatory Affairs Manager, Regulatory Team Leader, IND's Regulatory Affairs)) 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/contract-statistical-sas-programmer-contract-south-west-south-west-200645447.htmFri, 20 Nov 2009 15:27:49 +0000196611Leading Pharmaceutical company, situated in the South West are seeking a Contract Statistical SAS Programmer for a period of 12 months + The Contract Statistical SAS Programmer will; Consult with project team on statistical programming requirements for clinical trials projects sponsored by pharmaceutical or biotechnology companies. Designs SAS programs that develop data into prototypes/models to meet design specifications. Responsible for working on clinical trial projects sponsored by pharmaceutical, biotechnology, or medical device companies. Utilizes SAS and other analytical software in the creation of tables, figures and listings. Works closely with project managers and statisticians and participates as a project team member. Mentors less experienced statistical programmers. ESSENTIAL JOB FUNCTIONS 1. Consults with statisticians and sponsor to determine functional specifications for each project and prototype. 2. Uses SAS/GRAPH, SAS/BASE, SAS/MACRO, and SAS/STAT and other analysis software to design tables, listings and figures for the statistical reports to be generated and submitted to the sponsor. 3. Assists in the creation of Oracle or Oracle Clinical databases, as required. 4. Uses data step, merge/set array processing, formats/informats and functions (including numerical, character, date time and datetime functions, etc.) to develop and validate data. 5. Uses appropriate tools for customized report writing. 6. Develops, analyzes and creates well-formatted tables, listing and plots per specifications, and analyzes reports for consistency between text tables, listing and plots, and modifies same. 7. Performs quality control review of programs and command files. 8. Performs exploratory analyses using the prototype model provided by the statistician 9. Mentors and supports less experienced SAS programmers to design, develop, analyze, modify and create statistical prototypes with the system. EDUCATION/SKILL/EXPERIENCE REQUIREMENTS: Requires a BA/BS in math, science, biotechnology, or equivalent related experience, with very strong statistical programming experience in a Contract Research Organization (CRO), biotechnology, pharmaceutical or medical devices clinical trial experience. Strong SAS programming skills and experience in UNIX and/or personal computer environment are essential. Experience in Oracle/Oracle Clinical databases a plus. Requires strong modeling and analytical/conceptual skills. Ability to handle multiple tasks to meet deadlines in a high stress environment is essential. Requires strong organizational, presentation, documentation and interpersonal skills as well as a team-oriented approach. If you feel you have the credentials for this position, please get in contact ((KEYWORDS: SAS Programmer, Statistical Programmer, Statistical SAS Programmer, SAS Base, SAS Macro, Tables, Listings, Pharmaceutical, CRO, Oracle, Oracle Clinial)) 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-trial-administrator-north-west-200645437.htmFri, 20 Nov 2009 15:20:51 +0000196592Clinical Trial Administrator A fantastic opportunity to work for a young, fast growing company based in the North West. They are now looking for someone to be office based in their offices for a fixed term contract of 1 year which is highly likely to role. Ideally you will have 6 months experience as a CTA but this is not essential, you may be a recent graduate who can demonstrate your knowledge of Clinical Trials and the CTA role. Ideally you may have Phase III Renel therapy area experience. Key Responsiblities: • To provide comprehensive support to the clinical team for the set up and administration of clinical trials ensuring adherence to protocols and quality of information received. • Facilitating submissions of NHS R&D/PCT and ethics committee applications ( e.g. copying and filing regulatory documents and providing administrative support) • The efficient and accurate administrative processing of forms concerning data collection, payments and other materials with regard to clinical trials. Activities are based on the guidelines as described in company SOPs • Set up and maintenance of the trial documentation files, study records and tracking systems including electronic documents in accordance with ICH GCP and the company SOPs in such a way that any relevant information can be presented promptly during internal or external audits. • Be an internal focal point for Clinical Team, ensuring appropriate dissemination of information to team members • Communicate with all relevant internal and external contacts on a professional level: provide adequate information, consult the appropriate persons in case of problems and make a positive contribution to the decision making process. • Co-ordination of investigator meetings and related activities • Co-ordination of Clinical Trial supplies, dispatch and tracking Key Words: Clinical Trial Administrator Entry Level Graduate North West Renal CTA Contract http://www.newscientistjobs.com/jobs/job/clinical-project-director-spain-200644742.htmFri, 20 Nov 2009 14:16:51 +0000196317PROJECT DIRECTOR Experience * Minimum ten years experience in clinical biomedical research required * Minimum five years progressive employment-related experience in project scheduling, managing resources, and coordinating team activities required * Demonstrated experience with clinical development process, including clinical plan development, regulatory compliance, data management, and reporting through regulatory submissions, required * Thorough knowledge of regulatory requirements and ICH-GCP required * Prior project profit and loss management responsibility required; experience working with budgets, identifying out-of-scope project work and assessing in a timely manner the need for change order * Minimum of two years of experience managing professional staff or comparable project management experience required * Minimum of four years experience using computerized information systems required; experience with PC-Windows and word processing preferred * Read, write, and speak fluent English; in Europe, fluency in the language of the host country is also required Education * An undergraduate degree in health sciences from an accredited institution or equivalent degree plus required experience * An advanced degree (M.S., Ph.D., Pharm.D., M.D.) preferred * Targeted coursework in business issues (management, marketing, accounting), budgets, personnel management, negotiation skills, etc. required; Masters of Business Administration from an accredited institution or related coursework with employment experience is preferred Essential Functions * As a member of the region's management team, schedules and supervises clinical projects, provides leadership in the delivery of services to clients; reviews work produced by the project team; ensures staff fulfill their responsibilities in accordance with project contract and in-house policies, procedures and Standard Operating Procedures (SOPs) * As key participant in the team selling process, shares responsibility for growing business with existing clients and for identifying and closing projects with new clients; participates in presentations to the client and provides input to the project bid process * Takes lead role in day-to-day management of strategic projects such as clinical development programs and major domestic or international studies, and ensures that projects are delivered on time, within budget and according to client expectations * Provides significant input into pre-clinical data assessments, IND preparation, regulatory approval strategies, development program plans, clinical protocols, project plans and investigator brochures * As a senior member of the professional staff, keeps up with current industry practices and regulatory requirements; participates in the design and implementation of high-value solutions for clients on a billable basis; and provides leadership in the definition and delivery of well-managed clinical research projects * Ensures all internal and external issues regarding clinical research projects are properly addressed * As an experienced member of the client's professional staff, is an active mentor to one or more junior staff members and provides formal classroom as well as in-service training as requested by his/her functional leader * If assigned direct reports, schedules and reviews project tasks; provides leadership in the delivery of services to clients; ensures that staff fulfill their responsibilities in accordance with the client's policies, procedures, and SOPs; and ensures HR processes are properly implemented Responsibilities and Additional Duties To clients and prospective clients: * Takes a lead role in interfacing with clients and prospective client organizations, providing both technical and business credibility; is responsive to the client while assuring comprehensive management of quality clinical research projects * Maintains active, personalized, professional relationships with key client accounts through regular contact and value added consultation; monitors client satisfaction with project * For all assigned projects, works with client to develop a thorough and unambiguous understanding of tasks, project scope, and schedules To Project Teams: * Ensures each team is staffed with qualified personnel; complies with all contract provisions, ICH-GCPs, and regulatory requirements related to the project * Ultimately assures all project administration, study documentation, and reporting requirements are met in a timely manner * Participates in the development, review, and critique of key documents such as protocols, CRFs, analysis plans, reports, and regulatory submissions, and ensures review of same by appropriate team member(s) To the Regional Director and Business Management Team: * Is responsible for recommending, implementing, and achieving assigned objectives and budgets for all assigned project teams * In coordination with each functional leader for project team members, is responsible for the efficient and effective planning, implementation, and monitoring of project status to ensure optimal utilization of billable staff To Project Management team: * Passes on information to keep other project team leaders apprised of current events and status of managed projects, client relationships, communication with functional groups, and project teams within region * Provides clear team and individual goals and expectations and ensures that each member of the project management staff understands her/his responsibility to know and follow all SOPs and corporate policies To Other Regions: * Participates in the review and update of project management SOPs and the client's business processes; ensures operational consistency with defined company-wide practices Only successful applications will be responded to. http://www.newscientistjobs.com/jobs/job/clinical-project-director-netherlands-200644740.htmFri, 20 Nov 2009 14:16:39 +0000196315PROJECT DIRECTOR Experience * Minimum ten years experience in clinical biomedical research required * Minimum five years progressive employment-related experience in project scheduling, managing resources, and coordinating team activities required * Demonstrated experience with clinical development process, including clinical plan development, regulatory compliance, data management, and reporting through regulatory submissions, required * Thorough knowledge of regulatory requirements and ICH-GCP required * Prior project profit and loss management responsibility required; experience working with budgets, identifying out-of-scope project work and assessing in a timely manner the need for change order * Minimum of two years of experience managing professional staff or comparable project management experience required * Minimum of four years experience using computerized information systems required; experience with PC-Windows and word processing preferred * Read, write, and speak fluent English; in Europe, fluency in the language of the host country is also required Education * An undergraduate degree in health sciences from an accredited institution or equivalent degree plus required experience * An advanced degree (M.S., Ph.D., Pharm.D., M.D.) preferred * Targeted coursework in business issues (management, marketing, accounting), budgets, personnel management, negotiation skills, etc. required; Masters of Business Administration from an accredited institution or related coursework with employment experience is preferred Essential Functions * As a member of the region's management team, schedules and supervises clinical projects, provides leadership in the delivery of services to clients; reviews work produced by the project team; ensures staff fulfill their responsibilities in accordance with project contract and in-house policies, procedures and Standard Operating Procedures (SOPs) * As key participant in the team selling process, shares responsibility for growing business with existing clients and for identifying and closing projects with new clients; participates in presentations to the client and provides input to the project bid process * Takes lead role in day-to-day management of strategic projects such as clinical development programs and major domestic or international studies, and ensures that projects are delivered on time, within budget and according to client expectations * Provides significant input into pre-clinical data assessments, IND preparation, regulatory approval strategies, development program plans, clinical protocols, project plans and investigator brochures * As a senior member of the professional staff, keeps up with current industry practices and regulatory requirements; participates in the design and implementation of high-value solutions for clients on a billable basis; and provides leadership in the definition and delivery of well-managed clinical research projects * Ensures all internal and external issues regarding clinical research projects are properly addressed * As an experienced member of the client's professional staff, is an active mentor to one or more junior staff members and provides formal classroom as well as in-service training as requested by his/her functional leader * If assigned direct reports, schedules and reviews project tasks; provides leadership in the delivery of services to clients; ensures that staff fulfill their responsibilities in accordance with the client's policies, procedures, and SOPs; and ensures HR processes are properly implemented Responsibilities and Additional Duties To clients and prospective clients: * Takes a lead role in interfacing with clients and prospective client organizations, providing both technical and business credibility; is responsive to the client while assuring comprehensive management of quality clinical research projects * Maintains active, personalized, professional relationships with key client accounts through regular contact and value added consultation; monitors client satisfaction with project * For all assigned projects, works with client to develop a thorough and unambiguous understanding of tasks, project scope, and schedules To Project Teams: * Ensures each team is staffed with qualified personnel; complies with all contract provisions, ICH-GCPs, and regulatory requirements related to the project * Ultimately assures all project administration, study documentation, and reporting requirements are met in a timely manner * Participates in the development, review, and critique of key documents such as protocols, CRFs, analysis plans, reports, and regulatory submissions, and ensures review of same by appropriate team member(s) To the Regional Director and Business Management Team: * Is responsible for recommending, implementing, and achieving assigned objectives and budgets for all assigned project teams * In coordination with each functional leader for project team members, is responsible for the efficient and effective planning, implementation, and monitoring of project status to ensure optimal utilization of billable staff To Project Management team: * Passes on information to keep other project team leaders apprised of current events and status of managed projects, client relationships, communication with functional groups, and project teams within region * Provides clear team and individual goals and expectations and ensures that each member of the project management staff understands her/his responsibility to know and follow all SOPs and corporate policies To Other Regions: * Participates in the review and update of project management SOPs and the client's business processes; ensures operational consistency with defined company-wide practices Only successful applications will be responded to. http://www.newscientistjobs.com/jobs/job/faculty-positions-cancer-biology-fl-florida-200645280.htmFri, 20 Nov 2009 13:34:56 +0000196157The 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/research-assistant-institute-of-metabolic-science-cambridge-200644754.htmFri, 20 Nov 2009 10:53:18 +0000195289Metabolic Research Laboratories Department of Clinical Biochemistry Limit of tenure: 30th September 2014. Applications are invited for a Research Assistant position funded by the Medical Research Council to start on 4th January 2010 or as soon as possible thereafter. You will join an existing team headed by Dr Sadaf Farooqi to work in the Genetics of Obesity with a particular emphasis on the identification and functional characterisation of novel human mutations. Applicants should have a BSc in Biochemistry, Genetics or a related discipline. You will be required to have thorough experience of PCR, sequencing and molecular biology techniques including cloning, mutagenesis and cell culture. You will have good communication skills, flexibility to meet deadlines and the ability to work independently. Applications including CV, covering letter, names and addresses of three referees and a completed PD18 form including parts I, II and III (available by clicking the Apply Now button) should be sent to Ms Sue Barry at the address listed within the 'View Contact Details' section below. Formal enquiries may be made to Dr Sadaf Farooqi, email: sb770@medschl.cam.ac.uk. Telephone: 01223 762634. Please quote reference: RG05954. Closing date: 11 December 2009. The University values diversity and is committed to equality of opportunity.