Life Sciences jobs

• San Diego
• $110/hr
• Posted about 11 hours ago

Senior Manager, Regulatory Operations (Contractor) Job Summary A leading biopharmaceutical organization is seeking a seasoned Senior Manager of Regulatory Operations to support global regulatory submission processes and systems. This role will focus heavily on Regulatory Information Management (R...

• South San Francisco
• $140/HR - $200/HR
• Posted 21 days ago

Position Summary – GCP Quality Assurance Lead We’re seeking an experienced GCP Quality Assurance professional to provide strategic and operational leadership across all aspects of clinical QA. This role will ensure high standards of GCP compliance, patient safety, and data integrity from early de...

• Boston
• $175K - $195K
• Posted 22 days ago

Position: Associate Director, Regulatory Affairs Location: Hybrid in Lexington, MA or Remote (UK option available) Overview: An innovative biotechnology organization is seeking a strategic and experienced regulatory affairs professional to support the advancement of a growing RNA-based therapeuti...

• Gaithersburg
• $200,000 - $250,000 a year
• Posted 22 days ago

Head of Quality Position Overview: This position will be responsible for planning, organizing, and overseeing the Quality strategy to ensure the timely delivery of safe and effective products that meet all regulatory and compliance requirements. This role will ensure that processes required for t...

• Waltham
• $320,000-$358,000
• Posted 22 days ago

The Senior Medical Director/Global Safety Officer (GSO) will work closely with the DSPV leadership team and will provide strategic safety oversight, for the assigned investigational and/or marketed products, for Neuroscience portfolio.  Demonstrated prior career success as a product safety physic...

• San Francisco
• $290,000 - $350,000
• Posted 22 days ago

Reporting to the Senior Vice President of Global Regulatory Affairs and Quality Assurance, this position will serve as an in-house champion on GxP compliance as well as establish, maintain, and ensure effectiveness of quality programs and documentation to assure compliance in a GxP international ...

• San Francisco
• $250,000 - $300,000
• Posted 22 days ago

ESSENTIAL DUTIES AND RESPONSIBILITIES Support the preparation and implementation of regulatory strategies, for new drug Lead Clinical Quality oversight, including creation and revision of SOPs and training programs for GCP compliance Ensure involvement of Quality from early phases of development ...

• Waltham
• $200,00-$225,000
• Posted 22 days ago

Director, Clinical Quality Assurance, Pharmacovigilance The Director of CQA-PV is the supervisor of the Clinical Quality Assurance Department with responsibilities for quality oversight of the Post Marketing Good Pharmacovigilance Practices (GPvP) and Commercial Operations that contribute to the ...