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1-10 of 15 jobsHertfordshire
Company: Flame PharmaSalary: 1
America (US and Canadian IND etc). For more information please contact Flame Pharma on 0800 --- ---8 or email ----@----.com Key Words Regulatory Affairs, Senior Regulatory Affairs Consultant, Pharmacovigilance, Drug Safety... , Director, Manager, Management, Clinical Research, Clinical Trials, Medical, Clinical, CRO, Study Management, Clinical Management, Pharmaceutical, Career, Research, Berkshire, Job, Recruitment , Job Role: Other
Jobs similar to "cro ind": senior cro ind, senior director cro, senior flame cro
Hatfield
Salary: ??70,000-80,000 pa
America (US and Canadian IND etc). For more information please contact Flame Pharma on 0800 --- ---8 or email ----@----.com Key Words Regulatory Affairs, Senior Regulatory Affairs Consultant, Pharmacovigilance, Drug Safety... , Director, Manager, Management, Clinical Research, Clinical Trials, Medical, Clinical, CRO, Study Management, Clinical Management, Pharmaceutical, Career, Research, Berkshire, Job, Recruitment Start date: ASAP. Location
Contract: Permanent
for documents such as clinical study reports, Investigator Brochures and regulatory submission documents (IND... area training to internal and vendor (CRO) clinical project teams • Contribute to the development... , Immunology or Haemato-Oncology medicine, applicants must have pharmaceutical industry or CRO experience... and CRO sectors. An exclusive or preferred provider for many companies, only medics is established
Requirements: A leading Australian pharmaceutical company is looking for Clinical Research Physicians with industry experience to contribute to the medical management of R&D studies and development programs by providing medical and scientific leadership to cross-functi
Switzerland
Company: SEC RecruitmentSalary: NEGOTIABLE
research components of regulatory documents e.g., IND annual updates, IND safety updates, Investigator's... recruitment organisation working within the Pharmaceutical, Biotech and CRO industries SEC Recruitment Limited
Contract: Permanent
recommendations on the clinical research components of regulatory documents e.g., IND annual updates, IND safety... and CRO industriesSEC Recruitment Limited is acting as an Employment Agency and or Employment Business
Contract: Permanent
Geneva Basel Zurich Lausanne Bern Dijon Lyon London
Company: Key PeopleSalary: 70000 - 75000 Per Year
clinical trial related submission activities (e.g., IND, protocol submissions, amendments, response... of interaction with health authorities (Europe, US) and knowledge of regulatory submission formats (CTA, IND, CTD... " "pharmaceutical" "pharmaceutics" "cro" "clinical research organisation" "biotech" "small molecules" "translational
Experience: Manager (Manager/Supervisor of Staff)
Contract: Employee
Jobs similar to "cro ind": cro education europe
Authorization Applications (MAA) in the EU, IND annual reports, EMEA/CHMP documents, and scientific white papers... or international equivalent degree preferred and 5+ years of PK/Clin Pharm experience in Pharmaceutical R&D, CRO... or other relevant experience, or M.S. and 10+ years of PK/Clin Pharm experience in Pharmaceutical R&D, CRO
Experience: 5 years
Contract: Permanent
like Investigators' Brochures, briefing books, safety updates, IND/NDA submission documents, responses to Health Authorities questions. Accountable that program specific standards (e.g., CRFs, outsourcing specifications, data... organisation" "cro" "biotech" "clinical research" "clinical director" "tropical diseases" "switzerland" Start date: ASAP. Location: Basel, Bern, Zurich, Freiburg.
Contract: Permanent
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and regulatory registration. She/He will be responsible for the quality and adequacy of the tabular and written summaries and prepare in a timely fashion of data and documents (non-clinical part of IB, CTX, IMPD, IND, Briefing documents... , Expert reports etc.) of high quality for submission to Regulatory Authorities. The ideal candidate A minimum of 7 years experience in the Pharmaceutical industry or in a CRO Ideally a Doctorate level in Toxicology plus DVM
Requirements: Reporting directly to the Toxicology Director, the Senior Project Manager Toxicology will define, establish and sign-off the content of the preclinical safety studies to be performed from the selection of a lead candidate to registration.
Jobs similar to "cro ind": senior cro ind manager, senior ind impd, ind impd manager, toxicology cro director manager
standardization across studies within the project * Work on several clinical trials at the same time and/or manage safety poolings for IND updates, ISS/ISE icludingall trials ever done. Prepare or supervise preparation of Tables, Figures... , Biostatistics or related subject you should have a minimum of 3-4 years specific work experience within the pharmaceutical, biotechnology or CRO industry. Pharmaceutical, clinical trials, statistician, statistics, statistical, SAS
Requirements: Pharmaceutical, clinical trials, statistician, statistics, statistical, SAS, programmer, programming, statistics, statistician, biostatistics, biostatistician
Contract: Contract 6 months+