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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
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
Catabasis Pharmaceuticals, Inc. is dedicated to the discovery and development of innovative, effective and safe medicines to treat inflammatory and metabolic diseases. We are assembling a team of highly motivated and experienced professionals who are committed to improving the11/16/2014 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
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
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
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
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
Provides CMC regulatory direction and strategic technical regulatory input across all programs to ensure that all CMC regulatory requirements/commitments are met with respect to development and approval of all Forum products. This is a key, new regulatory role in a rapidly10/20/2014 Brighton, MA Save This Job
More information about this job: The right job isn?t about location or benefits or responsibilities. The right job is about personality, character, motivation, and fulfillment. It?s about what inspires us, what we?re passionate about. At Fluidigm, we?re passionate about life.10/28/2014 South San Francisco, CA Save This Job
Department:Regulatory, Clinical and Quality Job Reports To:Director, Quality Assurance & Regulatory Compliance FLSA:Exempt POSITION OVERVIEW Job Purpose: The Regulatory Affairs Manager facilitates the initial approval and continued regulatory support necessary CardioFocus11/26/2014 Marlborough, MA 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
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
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
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
Job Description This position is responsible for facilitating oversight, evaluation and performance of all equipment, facilities, systems, utilities and product/process validation for Protein Sciences Corp. The encumbant will be the SME (subject matter expert) and help11/17/2014 Meriden, CT 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 ? that10/26/2014 Fremont, CA Save This Job
Department: Global Alliance Management Reports To: Vice President, Global Alliance Management Job Summary / Overview: This position is responsible for overseeing the execution of all product development activities from initiation of the project through product launch11/18/2014 Schaumburg, IL Save This Job
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