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Clinical Affairs Manager Jobs

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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?

8/1/2016  Boston, MA  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

8/28/2016  Cambridge, MA  Save This Job

Regulatory Affairs Manager

Alder Biopharmaceuticals

The responsibilities of this newly created position will focus on supporting the development and implementation of regulatory strategies for Alder BioPharmaceuticals development programs. This includes responsibility for preparation and submission of regulatory documentation to

8/30/2016  Bothell, WA  Save This Job

Regulatory Affairs Specialist (U.S.)

Globus Medical

Location:Audubon, PA Job Code:RAPMKB0515 Description The Regulatory Affairs Specialist assists in writing, submitting and gaining clearance for 510(k) submissions and approval for IDE/PMA submissions to the Food and Drug Administration (FDA) for class II and class III products.

8/29/2016  Audubon, PA  Save This Job

Manager - Regulatory Affairs

Sciformix Corporation

Manager - Regulatory Affairs (United States; Russia; Egypt; Turkey; UAE; Israel; Saudi Arabia) Responsibilities Manager positions will be responsible for administering the day-to-day Regulatory Affairs operations. Responsibilities may include: Directly or indirectly managing

8/23/2016  Westborough, MA  Save This Job

Group Manager, Regulatory Affairs

Globus Medical

Location:Audubon, PA Job Code:GMRALB0816 Description The Group Manager, US Regulatory, is responsible for preparing, filing and gaining approval of 510(k), IDE, and PMA submissions to the U.S. Food and Drug Administration (FDA) for class II and class III products. This position

8/29/2016  Audubon, PA  Save This Job

Manager, Educational Affairs

Cleveland HeartLab

CLEVELAND HEARTLAB SEPTEMBER 9, 2016 JOB OPENINGS Cleveland HeartLab, Inc. (CHL) is a premier next-generation clinical reference laboratory committed to advancing cardiovascular risk assessment through unique and proprietary diagnostic tests. We focus on novel inflammatory and

9/27/2016  Cleveland, OH  Save This Job

Medical Director, Regulatory Affairs

Sagent Pharmaceuticals

Application Deadline: August 31, 2016 Location: Schaumburg, IL Job Summary / Overview: In the capacity of Medical expert, the Medical Director is responsible for bringing greater medico-clinical based product insights to the organization. In addition, this role provides greater

8/23/2016  Schaumburg, IL  Save This Job

Manager - GCP Quality Assurance

Argos Therapeutics

Manager ? GCP Quality Assurance About Us Manager ? GCP Quality Assurance Description Argos Therapeutics is a biopharmaceutical company focused on the development and commercialization of fully personalized immunotherapies for the treatment of cancer and infectious diseases

8/15/2016  Durham, NC  Save This Job

Program Manager, Surgeon Education and Training

Globus Medical

Location:Audubon, PA Job Code:PMSEJL0816 Description The Program Manager is responsible for the strategic plan development and tactical execution of medical education programs for assigned business segment(s). Responsible for the creation, implementation, promotion and

8/29/2016  Audubon, PA  Save This Job

Senior Manager/Associate Director, Pharmaceutical Development

ChemoCentryx, Inc.

Working with CCXI Senior Management, Contract Development Organizations and selected Consultants, this individual is responsible for the development and overseeing the execution of all the technical activities associated with product development in support of Clinical Development

9/8/2016  Mountain View, CA  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

7/31/2016  Bothell, WA  Save This Job

Senior Manager/Associate Director, Commercial Strategy

Alder Biopharmaceuticals

This position will report to the Vice President of Commercial Strategy who overseas New Product Marketing, Market Research, Forecasting, Analytics and Competitive Intelligence functions for the company. The role will be primarily responsible for forecasting Alder?s lead

7/31/2016  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

7/31/2016  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

7/27/2016  New York, NY  Save This Job

Director of Quality Assurance and Regulatory Affair

TeraRecon

Location:USA - CA Company Order Number:397 # of openings:1 Description About the Company TeraRecon is the largest independent, vendor neutral medical image viewing solution provider with a focus on advanced image processing innovation. TeraRecon iNtuition and iNteract+ solutions

7/30/2016  San Mateo, CA  Save This Job