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The Director of Clinical Affairs is responsible for managing the analysis of clinical studies and work closely with Research/Development, Engineering, and RA/QA personnel on clinical studies. Responsibilities: Evaluate the progress of research programs. Manage clinical research12/5/2014 Fremont, CA Save This Job
Summary of Position The Director, Regulatory Affairs is the regulatory representative on the Product Development Teams providing regulatory support and advice. The Director will facilitate regulatory strategy development and implementation, take the lead on regulatory10/19/2014 Gaithersburg, MD Save This Job
SUMMARY: The Medical Directors, Medical Affairs, will lead a broad range of medical affairs activities to plan for and support the launch of patiromer. Reporting to the VP, Medical Affairs and working closely with both the Commercial and Clinical Development groups, the Medical10/21/2014 Redwood City, CA Save This Job
Description: Reporting to the Vice President of Regulatory Affairs, the successful candidate will provide expertise in translating regulatory requirements into practical, workable plans for development stage oncology related drugs and biologics. Candidate will have primary11/10/2014 San Francisco, CA Save This Job
SUMMARY: The core focus for the appointee will be both the strategic and tactical execution of new clinical trials for patiromer and/or the development and execution of a clinical development plan to support a European MAA and to support a pediatric indication. Ideally, the10/21/2014 Redwood City, CA Save This Job
Merrimack is a biopharmaceutical company discovering, developing and preparing to commercialize innovative medicines paired with companion diagnostics for the treatment of cancer. Merrimack seeks to gain a deeper understanding of underlying cancer biology through its systems10/27/2014 Cambridge, MA Save This Job
Department: Regulatory Affairs Location: Emeryville, CA Position Summary This position is primarily responsible for developing, coordinating and implementing regulatory strategies for new product development registrations, postmarketing change and maintenance requirements,12/8/2014 Emeryville, CA Save This Job
About Acceleron: Acceleron is a publicly traded, clinical stage biopharmaceutical company focused on the discovery, development and commercialization of novel protein therapeutics for cancer and rare diseases. The company is a leader in understanding the biology of the TGF-?11/16/2014 Cambridge, MA Save This Job
This Associate Medical Director level position requires the ability to work with supervision, in responsibilities associated with all aspects of design, setup, monitoring, and analysis of Phase 1 - 3 clinical trials. This person must have the ability to interact effectively with11/16/2014 Mountain View, CA Save This Job
We are seeking a highly experienced candidate with an advanced medical and science degree, preferably in oncology, to lead our effort into the clinical development of the company immunodiagnostic assay pipeline, and provide strategic guidance in regulatory affairs and compliance.10/15/2014 Emeryville, CA Save This Job
The position is responsible for providing Regulatory Affairs direction for FORUM?s products. They will author, review and edit regulatory submissions, develop regulatory strategy in conjunction with business objectives and functional management, and drive timelines and10/20/2014 Brighton, MA Save This Job
ID 2014-1250 # of Openings 1 Department Clinical Affairs Posted Date 10/15/2014 Job Location US-MA-Marlborough More information about this job: Overview: The Director of Medical Affairs will report to the Chief Medical Officer, Oxford Immunotec, and will be based at the USA11/17/2014 Marlborough, MA Save This Job
SUMMARY: Senior Manager/Associate Director, Pharmaceutical Development is responsible for the design, development and optimization of formulation and process for drug candidates to support the manufacture of pre-clinical, clinical, registration and commercial manufacturing. The10/21/2014 Santa Clara, CA Save This Job
Department: Regulatory Affairs Job Title: Director-, Drug Safety Job Location: Operations Description: Cytokinetics, Inc. is a clinical-stage biopharmaceutical company dedicated to the discovery and development of novel small molecule therapeutics that modulate muscle function10/14/2014 South San Francisco, CA Save This Job
Department: Project Management Job Title: Associate Director, Project Management Job Location: South San Francisco Description: Cytokinetics, Inc. is a clinical-stage biopharmaceutical company dedicated to the discovery and development of novel small molecule therapeutics that10/14/2014 South San Francisco, CA Save This Job
Position Overview The Senior Director, HEOR will be responsible for setting the HEOR strategy and for the successful execution of HEOR projects and deliverables through partnership with the following functional areas: the Commercial organization, the Managed Markets-assigned11/20/2014 Santa Clara, CA Save This Job
Department: Corporate Communications/ Investor Relations Job Title: Director/Sr. Director, Corporate Communications & Investor Relations Job Location: South San Francisco Description: Cytokinetics, Inc. is a clinical-stage biopharmaceutical company dedicated to the discovery and10/14/2014 South San Francisco, CA Save This Job
SUMMARY: Reporting to the Chief Medical Officer, the Executive Director will serve as the Head of Drug Safety and Pharmacovigilance (PV) Department and will have primary responsibility for the operational and strategic assessment of safety information and the implementation of10/21/2014 Redwood City, CA Save This Job
Region: Texas (Texas, Oklahoma, Arkansas, Louisiana) Position Overview The Medical Science Director (MSD) will participate in the strategic development and tactical execution of plans to engage scientific thought leaders and act as a conduit for providing accurate and updated11/20/2014 TX Save This Job
Region: TBD SUMMARY: The Medical Science Director (MSD) will participate in the strategic development and tactical execution of plans to engage scientific thought leaders and act as a conduit for providing accurate and updated clinical, scientific and medical information to11/20/2014 Redwood City, CA Save This Job