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Senior Manager, Regulatory Affairs
Sagent Pharmaceuticals
Department: Regulatory Affairs Classification: Exempt Reports To: Sr. Director, Regulatory Affairs Job Summary / Overview: Serves as the primary regulatory interface with FDA, Partners and internal team. Ensure the business needs for the assigned products are met by
3/19/2013 Schaumburg, IL Save This JobSr. Associate, Regulatory Affairs
Sagent Pharmaceuticals
Department: Regulatory Affairs Classification: Exempt Reports To: Sr Manager, Regulatory Affairs AND/OR Associate Director Regulatory Affairs Job Summary / Overview: The role is primarily responsible for the management and support of Pre and Post approval regulatory
3/19/2013 Schaumburg, IL Save This JobManager, Regulatory Affairs, Labeling
Sagent Pharmaceuticals
Department: Regulatory Affairs Classification: Exempt Reports To: Associate Director Regulatory Affairs Job Summary / Overview: This role is primarily responsible for managing the development of labeling and managing key labeling systems and processes to support labeling
3/19/2013 Schaumburg, IL Save This JobSr. Manager, Quality Assurance and Regulatory Affairs
Promega
Tracking Code 1864 Job Description JOB OBJECTIVES: Responsible for all aspects of the PBS quality system, encompassing product quality as well as the quality of processes and services throughout the organization. ACCOUNTABILITIES: ? Accountable for the development and
4/29/2013 Sunnyvale, CA Save This JobDirector of Regulatory Affairs
TeraRecon
Description About the Company: TeraRecon ushered in the genre of thin-client advanced visualization for CT and MRI with the invention of the AquariusNET Server in 2001 and has since grown to be the premier provider of volumetric image management and decision support solutions.
3/12/2013 Foster City, CA Save This JobSenior Manager/Associate Director, Regulatory Affairs (13-120)
FibroGen
Description: Review, provide comments on, and prepare documents for submission to FDA and international regulatory authorities including protocols, investigator brochures, nonclinical and CMC amendments, and other regulatory documents. Lead teams on the preparation, review and
5/16/2013 San Francisco, CA Save This JobDirector/Manager Veterinary Support
Putney
Description Putney is seeking an experienced Director/Manager Veterinary Support to support delivery of Putney?s educational and financial goals and generate awareness of Putney?s companion animal pharmaceuticals; this will be done in collaboration with the veterinary support,
4/16/2013 Portland, ME Save This JobManager, R&D (#13-8004)
AccessClosure
JOB DESCRIPTION ( 13-8004) TITLE: Manager, Research & Development FLSA: Exempt LOCATION: Mountain View, CA POSTING DATE: 1/14/2013 SUMMARY/RESPONSIBILITIES: SUMMARY: Plans, directs, and coordinates activities of designated project to ensure that goals or objectives
5/6/2013 Mountain View, CA Save This JobClinical Trial Manager
Theraclone Sciences
Theraclone Sciences is a Seattle-based biotechnology company focused on the development of novel, therapeutic, human-antibodies for the treatment of infectious disease and cancer, and as a basis for vaccine development. Theraclone is a privately held company with venture
4/3/2013 Seattle, WA Save This JobSr Marketing Manager, Molecular
Diagnostic Hybrids
ategory: Marketing Description: Join a growing, innovative healthcare diagnostics leader! We have an opportunity for a Senior Marketing Manager in our Molecular business unit. The ideal candidate will have experience in molecular diagnostics and a strong understanding of the
5/10/2013 San Diego, CA Save This JobSenior Manager, Clinical Operations
Acceleron Pharma
About Acceleron: Founded in 2003, Acceleron Pharma, Inc. is a privately-held biopharmaceutical company committed to discover, develop, manufacture and commercialize novel protein therapeutics for orphan diseases and cancer. We have internally discovered and developed 4 products
4/10/2013 Cambridge, MA Save This JobManager, Operations
OmniSYS
Position based in Greenville Operations Facility Job Description Provides guidance to the operational activities of the audit and compliance teams with the objective of maximizing growth and profitability. Strong leader with proven operational experience. Position reports to
3/26/2013 Greenville, TX Save This JobProject Manager
Outcome Software, Inc.
Description Purpose: With supervision from Management, the Project manager (PM) role is to implement agreed upon strategies for the management of national or international internet-based outcome studies with pre-specified timelines and budgets. The PM leads the project team and
3/30/2013 Cambridge, MA Save This JobProject Manager
Outcome Software, Inc.
Description Purpose: With supervision from Management, the Project manager (PM) role is to implement agreed upon strategies for the management of national or international internet-based outcome studies with pre-specified timelines and budgets. The PM leads the project team and
3/30/2013 Cambridge, MA Save This JobSenior Contracts Manager
DriveCam
Job Code: 13-028 Position Summary: DriveCam is seeking an experienced contracts manager to assist the Legal Department on strategic transactions, contracts review, compliance and other matters. The Senior Contracts Manager will have significant responsibility for providing
5/10/2013 San Diego, CA Save This JobTax Manager
DriveCam
Job Code: 13-019 Position Summary: The Tax Manager will be responsible for the Company?s tax compliance, tax planning, accounting for income taxes and coordinating any required tax audits. The Company operates in most states and internationally. Responsibilities: ?
4/10/2013 San Diego, CA Save This JobProduct Specialist
Tactile Systems Technology
Department: Sales Reporting Relationship: Regional Sales Manager Scope of Supervision: Not applicable Other Key Relationships: Marketing, Product Strategy, Regulatory Affairs, Reimbursement Operations, Payer Relations, Clinical Specialists, Patients, Physicians,
4/6/2013 Minneapolis, MN Save This JobClinical Data Monitor
Globus Medical
Description Clinical Data Monitor The position is responsible for performing monitoring activities associated with all ongoing Class III FDA-related clinical studies. This individual will need to perform site monitoring visits by adhering to the schedule established in
3/26/2013 Audubon, PA Save This JobMedical Writer
CoreLab Partners
Overview: Main responsibility involves reviewing protocols, writing Charters and Imaging Manuals, and reviewing the technical and medical components of study-related documents. Responsibilities: Author Independent Review Charters (Charters), Imaging Manuals (if applicable)
2/5/2013 Princeton, NJ Save This Job