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Regulatory Affairs Program Manager Jobs

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Senior Manager, Regulatory Affairs

Relypsa

Company Overview Relypsa, Inc. is a late clinical-stage pharmaceutical company leading the discovery and development of novel non-absorbed polymeric drugs for important applications in cardiovascular and renal diseases. Relypsa's lead product candidate is patiromer, a

5/17/2016  Redwood City, CA  Save This Job

MANAGER, FP&A: CLINICAL RESEARCH & DEVELOPMENT, REGULATORY AFFAIRS &

Cytokinetics

COMPLIANCE Department: Finance Job Location: South San Francisco Cytokinetics is a late-stage biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators as potential treatments for debilitating diseases in which muscle

5/9/2016  South San Francisco, CA  Save This Job

Senior Regulatory Program Manager

Ossia, Inc.

Engineering ? Bellevue, Washington The Role: As an Ossia Senior Regulatory Program Manager, you will be responsible for spearheading certification effort for this new breakthrough technology. This role requires expertise in US and international regulatory processes, RF and

6/13/2016  Bellevue, WA  Save This Job

Sr. Clinical Supply Manager

Merrimack Pharmaceuticals

Clinical Operations Cambridge, MA, United States Merrimack is a fully integrated biopharmaceutical company that views cancer as a complex engineering challenge. Through systems biology, which brings together the fields of biology, computing and engineering, Merrimack aims to

6/21/2016  Cambridge, MA  Save This Job

Clinical Trial Manager

Promedior

Job Description The Clinical Trial Manager in collaboration with the Clinical Project Manager, contributes to the operational execution of clinical studies to ensure delivery on time, within budget, and of high quality in compliance with ICH/GCP, Regulatory Authorities?

5/29/2016  Boston, MA  Save This Job

Senior Manager, GCP Compliance

Alder Biopharmaceuticals

This newly created position reports to the Director, Quality Assurance Compliance and is responsible for assuring GCP compliance with Alder SOPs, ICH and FDA/EMA regulations. Specific responsibilities will include: Provide GCP compliance support: participate in Clinical Project

6/24/2016  Bothell, WA  Save This Job

Senior Project Manager

Alder Biopharmaceuticals

This newly created position will work closely with the VP Program & Portfolio Management (PM) to provide specialized cross-functional PM leadership for Alder?s drug development programs through expert planning, risk mitigation and execution. Collaborates with functional project

5/25/2016  Bothell, WA  Save This Job

Rare Disease Manager - NY Metro (3541)

Aegerion Pharmaceuticals, Inc.

Career Opportunities: Rare Disease Manager - NY Metro (3541) Req Id 3541 - Posted 06/15/2016 - United States - New York - New York City - Sales The field based Rare Disease Manager will be responsible for preparing the market, educating customers and ultimately performing

6/22/2016  New York, NY  Save This Job

Rare Disease Manager - NJ/Phila/Staten Island (3621)

Aegerion Pharmaceuticals, Inc.

Req Id 3621 - Posted 05/05/2016 - United States - New Jersey - Newark - Sales ? Job Description Print Preview Apply Apply using LinkedIn? Save Job Email Job to Friend Return to List The field based Rare Disease Manager will be responsible for preparing the market,

6/22/2016  Newark, NJ  Save This Job

Quality Assurance Complaint Specialist

Sagent Pharmaceuticals

Application Deadline: May 31, 2016 Location: Schaumburg, Illinois, USA Job Summary / Overview: To provide Quality Assurance support and guidance for customer complaints received by managing the Sagent customer complaint program. Proactively support the existing quality systems

5/15/2016  Schaumburg, IL  Save This Job