Life Sciences jobs

• Madison
• $225,000
• Posted 2 days ago

Head of Commercial Manufacturing - Xenotransplantation Location: Madison Wisconsin Level: Senior / Vice President An innovative biotechnology company is redefining the future of organ transplantation through cutting-edge xenotransplantation. We are seeking a seasoned executive with a track record...

• San Francisco
• $120/hr
• Posted 3 days ago

Program Director, Clinical Operations (Contract) Location: South San Francisco/San Diego, CA or Remote This is a 6-month contract. Pay rate range is $120s A dynamic biotech organization is seeking a seasoned Program Director of Clinical Operations to provide strategic leadership across one or mor...

• South San Francisco
• Targeting $110/hr
• Posted 3 days ago

Associate Director, Data Standard & Statistical Programming (Contractor) Location: Remote Job Summary A fast-paced biotech organization is seeking an experienced Associate Director of Data Standards & Statistical Programming (DSSP) to lead statistical programming efforts across clinical programs....

• San Diego
• $110/hr
• Posted 3 days 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 23 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...

• San Francisco
• $80.00-$100.00 per hour
• Posted 24 days ago

POSITION SUMMARY: The Statistical Programming Consultant will be the lead programmer for multiple clinical studies and collaborating with study statistician, data managers and the other functions in the clinical study team. This will be a remote opportunity.  ESSENTIAL DUTIES AND RESPONSIBILITIES...

• San Francisco
• $85.00- $125.00 per hour
• Posted 24 days ago

POSITION SUMMARY: The Biostatistics Consultant is the lead statistician for all phases of the clinical development studies in collaborating across all functions within clinical development and CMC. This will be a remote opportunity.  ESSENTIAL DUTIES AND RESPONSIBILITIES: Effectively lead all sta...

• Boston
• $175K - $195K
• Posted 24 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 24 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 24 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...

• South San Francisco
• $95 - $120 per hour
• Posted 24 days ago

SR CTM Experience  Minimum of 7 years of related industry experience in Clinical Operations with increasing responsibility and scope  Minimum of 2 years study management experience in clinical operations at a Sponsor company  Experience in selecting, managing, and overseeing sites, CROs, specialt...

• San Francisco
• $290,000 - $350,000
• Posted 24 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 24 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 24 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 ...