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SUMMARY: The Senior Director of Regulatory Affairs reports directly to the Executive Director, Regulatory Affairs. This position coordinates departmental planning, manages multiple project teams and provides the regulatory strategies to ensure appropriate implementation of key9/17/2014 Redwood City, 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 regulatory10/15/2014 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 Medical10/17/2014 Redwood City, CA Save This Job
Description: Cytokinetics, Inc. is a clinical-stage biopharmaceutical company dedicated to the discovery and development of novel small molecule therapeutics that modulate muscle function for the potential treatment of serious diseases and medical conditions. Working9/9/2014 South 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, the10/17/2014 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 systems10/21/2014 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,8/13/2014 Emeryville, CA 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 with9/1/2014 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.9/13/2014 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 and9/16/2014 Brighton, MA Save This Job
SUMMARY: The Senior Director, Medical Science Liaison (MSL) Team Leader will be responsible for building the Company?s MSL team and for developing both strategies and tactical execution plans to engage scientific thought leaders and to develop partnerships with key scientific9/17/2014 Redwood City, CA Save This Job
Description: FibroGen seeks a goal driven, dynamic individual in the Regulatory Affairs department. This position provides proactive support and technical assistance to more experienced regulatory personnel and reports directly to either an Associate Director or Director of9/7/2014 San Francisco, CA 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. The10/17/2014 Santa Clara, CA Save This Job
Department: Regulatory Affairs Job Title: Manager/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 muscle10/9/2014 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 that9/9/2014 South San Francisco, CA Save This Job
Position Description This position is to participate in pricing and market access activities, including value demonstration for Aegerion product(s). This position will design and conduct analyses that demonstrate the relative economic and humanistic value of Aegerion medicines.8/24/2014 Cambridge, MA 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 and9/9/2014 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 of9/17/2014 Redwood City, CA Save This Job
Job code: 2014-04 Zosano Pharma, Inc. is a specialty pharmaceutical company creating better products utilizing innovative drug delivery technology. We have developed a user-friendly, simple, and needle-free transdermal delivery system consisting of a patch and applicator ? that9/20/2014 Fremont, CA Save This Job
Dynamic pharmaceutical known for scientific excellence, located in MA, seeks a professional with at least a BS in Health Sciences (MS preferred) with 10+ yrs. experience in clinical quality assurance including 5 years of supervisory background. Comprehensive knowledge of GCP10/16/2014 Brighton, MA Save This Job