Life Sciences jobs

• San Francisco
• $215,000 - $280,000
• Posted 3 days ago

  Position Description: The Director of Regulatory Affairs will serve as the global regulatory lead (GRL) on several immunology programs and will be responsible for developing the global regulatory strategy in collaboration with key internal stakeholders, as well as tactical implementation of tha...

• Boston
• $180,000-215,000
• Posted 15 days ago

The Clinical Project Manager / Sr. Clinical Project Manager (CPM) provides operational leadership of one or more clinical trials from protocol development through clinical study report, and ensure activities are executed in accordance with the protocol, ICH/GCP guidelines, applicable regulations,...

• San Diego
• $167,000.00-$241,925.00
• Posted 16 days ago

Serves as the lead reviewer for medical education and commercial advertising and promotional materials for product, disease state, and training/education programs. Leads cross-functional collaboration to ensure appropriate reviews take place and timely submissions are made to OPDP. Work closely w...

• Waltham
• $200,00-$225,000
• Posted 21 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 ...

• Cranbury
• 285000
• Posted about 1 month ago

Senior Director, Global Regulatory Lead    Our client is growing, rare genetic disease company based in the Princeton area, dedicated to developing treatments across hematology, cardiology, and other undisclosed diseases. With a pipeline of multiple late-stage programs and BLAs slated for the com...

• Boston
• $180,000-$240,000
• Posted about 1 month ago

Position Overview: As the Associate Director / Director of Regulatory Strategy, you will play a critical role in driving the development and execution of regulatory strategies for our rare disease therapeutic programs. Your expertise and leadership will be instrumental in navigating the complex r...

• San Carlos
• TBA. Estimated range: 200-235K base
• Posted about 2 months ago

Director, Regulatory Affairs Location: San Mateo, CA Position Overview: The Director of Regulatory Affairs will lead global regulatory activities with a focus on clinical filings. This role involves guiding regulatory strategy, managing submissions, supporting clinical trial applications, and ens...

• South San Francisco
• 230000
• Posted 2 months ago

Company Overview The Company’s lead product candidate has received Fast Track Designation and Orphan Drug Designation from the U.S. Food and Drug Administration for both idiopathic pulmonary fibrosis (IPF) and primary sclerosing cholangitis (PSC) and Orphan Drug Designation from the European Medi...

• Boston
• $180,000-$230,000
• Posted 2 months ago

AD/Director, Regulatory Operations & Affairs About the Role We are seeking a highly skilled, and experienced AD/Director of Regulatory to join our growing clinical team. This hands-on position will be responsible for overseeing and managing all global regulatory activities to ensure compliance wi...

• New Jersey
• $207,000.00 to $289,867.00 per year
• Posted 3 months ago

Overview Reporting to the Executive Director Quality GMP Compliance, the Director, Quality Operations will play a key role in managing QA oversight activities. He/she will be responsible for Quality related activities for commercial products including transition from development (Phase III) into ...

• Lexington
• $130,000-$140,000
• Posted 5 months ago

Manager, Clinical Supply Chain Management Reporting to the Director, Clinical Supply Chain the Manager, Clinical Supply Chain Management will be responsible for establishing and managing the end to end clinical supply for clinical studies/programs in various phases. Successful candidates will pos...