Life Sciences jobs

• South San Francisco
• $140/HR - $200/HR
• Posted about 10 hours 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...

• Cambridge
• $195,000
• Posted 1 day ago

Associate Director, Clinical Operations Cambridge, MA Clinical Development / A growing biotech organization is seeking a resourceful and collaborative Associate Director to join its Clinical Operations team and support programs across a diverse portfolio of programs revolutionizing the field of o...

• San Francisco
• $80.00-$100.00 per hour
• Posted 1 day 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...

• Cambridge
• $220,000
• Posted 1 day ago

Associate Director, Clinical Science Cambridge, MA A growing biotech organization is seeking a resourceful and collaborative Associate Director/Director as the first Clinical Science member of the Medical team, to support programs across a diverse portfolio of programs revolutionizing the field o...

• San Francisco
• $85.00- $125.00 per hour
• Posted 1 day 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...

• Massachusetts
• 0
• Posted 1 day ago

Senior Manager, Medical Writing Job Description The Senior Manager, Medical Writing is a key member of the Clinical Development organization, responsible for independently authoring, managing, and delivering high-quality clinical documents across all phases of development. In addition to hands-on...

• Boston
• $175K - $195K
• Posted 1 day 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...

• Cranbury
• 300000
• Posted 1 day ago

Join our team dedicated to curing rare diseases! We value our team members' growth and well-being as much as our scientific progress. We seek collaborative, hands-on individuals passionate about making a difference for patients. This is an opportunity to be part of a small, dynamic team and contr...

• Gaithersburg
• $200,000 - $250,000 a year
• Posted 1 day 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 1 day 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 1 day 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 1 day 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 1 day 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 1 day 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 ...