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Director/Associate Director - Regulatory Affairs (United States; Russia; Egypt; Turkey; UAE; Israel; Saudi Arabia) Responsibilities Setting regulatory strategy and translating these strategies into executable plans for specific departments/areas of responsibility Providing8/23/2016 Westborough, MA Save This Job
TARIS Biomedical is a unique therapeutically-focused urology company developing drug-device combination products for the treatment of genitourinary diseases. This individual will provide leadership and expertise for regulatory activities that support assigned TARIS? pipeline8/27/2016 Lexington, MA Save This Job
Department: Regulatory Affairs Position Type / FLSA Status: Full Time / Exempt Location: Emeryville, CA Position Summary This position is primarily responsible for developing, coordinating and implementing regulatory strategies for new product development registrations,8/1/2016 Emeryville, CA Save This Job
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 greater8/23/2016 Schaumburg, IL Save This Job
Intra-Cellular Therapies, Inc. (ITI) is an equal opportunity employer. Applicants may send their CV/resume and cover letter in plain text or as Microsoft Word attachments by e-mail to firstname.lastname@example.org/14/2016 New York, NY Save This Job
Department: Regulatory Affairs Job Title: Regulatory Affairs Associate Reports To: Senior Director, Regulatory Affairs Description: Position Overview: This position is responsible for the preparation, archival and tracking of regulatory submissions prepared in support of its8/24/2016 Philadelphia, PA Save This Job
Tracking Code 273-093 Job Description We are seeking a bright, driven and motivated individual to join our team as Senior Director, Clinical Affairs. Responsibilities: Provide oversight of clinical studies performed for product registration purposes, research, and/or marketing8/6/2016 Lexington, MA Save This Job
SENIOR DIRECTOR, GLOBAL REGULATORY AFFAIRS We have an exciting newly created opportunity for an outstanding Head of Regulatory Affairs in our dynamic, successful and fast growing pharmaceutical company. ABOUT ENANTA Enanta Pharmaceuticals is a research and development-focused7/31/2016 Watertown, MA Save This Job
Application Deadline: October 31, 2016 Location: Schaumburg, Illinois, United States Job Summary: Leads the Quality Systems team and provides guidance and direction to all after-market Sagent product quality issues. Partners with Sagent?s Global Alliance Management9/22/2016 Schaumburg, IL Save This Job
Company Overview Relypsa, Inc. is a biopharmaceutical company focused on the discovery, development and commercialization of polymeric medicines for patients with conditions that are often overlooked and undertreated and can be addressed in the gastrointestinal tract. The8/24/2016 Redwood City, CA Save This Job
Assoc. Director, Clinical Operations? Help Please fill in the information below and use the navigational buttons to continue. Warning: Using your browser's Back and Forward buttons may produce undesirable results. Associate Director, Clinical Operations About Acceleron:8/9/2016 Cambridge, MA Save This Job
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 Development9/8/2016 Mountain View, CA Save This Job
TARIS Biomedical is a unique therapeutically-focused urology company developing drug-device combination products for the treatment of genitourinary diseases. The Associate Director of Clinical Quality Assurance will provide leadership and expertise to support TARIS? pipeline8/27/2016 Lexington, MA Save This Job
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 Project7/31/2016 Bothell, WA Save This Job
Reports to: Vice President, Clinical Development Education: Board certification in Internal Medicine, and preferably additional Board Certification in Pulmonary Medicine or Oncology Job Description This role represents a unique opportunity for a physician experienced in8/1/2016 Boston, MA Save This Job
JOB OVERVIEW The Statistician will provide statistical leadership in design, analysis, interpretation, and reporting of clinical trials and predictive modeling of pharmacogenomics data that help build the business. This position is in the Medical Affairs and Clinical9/1/2016 Mason, OH Save This Job