All jobs near California in the Life Sciences sector

• South San Francisco
• $80 - 120/Hour
• Posted about 2 months ago

Vendor Oversight Manager Contractor POSITION SUMMARY The Vendor Oversight Manager Contractor is responsible for developing and executing Vendor Governance Oversight process and strategies within Clinical Development Operations, considering vendor performance and business risk.  The candidate will...

• San Francisco
• $175000-190000
• Posted about 2 months ago

The Associate Director is responsible for the development and approval of all US promotional materials and serving as the promotional regulatory expert with marketing, legal, and medical teams to ensure that promotional practices are consistent with regulatory guidelines and support business obje...

• San Francisco
• $260,000 - $310,000 a year
• Posted 2 months ago

Senior Director, Biostatistics Full Time Onsite 4 days per week. Relocation assistance is available.   Summary: The Senior Director, Biostatistics will lead Biostatistics and Biometrics, overseeing statistical support for therapeutic development. Collaborating with Clinical Development, Regulator...

• South San Francisco
• $95 - $120 per hour
• Posted 3 months 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...

• South San Francisco
• $190,000 - $215,000
• Posted 4 months ago

POSITION SUMMARY Reporting to the Sr. Dir., Clinical Outsourcing, this position will be responsible as required for supervising staff in the Clinical Outsourcing group. This position will work with internal teams (e.g. Clinical Development, Clinical Science, Legal, Finance and Procurement Departm...

• San Francisco
• $290,000 - $350,000
• Posted 5 months 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 5 months 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 ...

• San Francisco
• $255,000 - $300,000
• Posted 5 months ago

POSITION SUMMARY Guide the overall CMC regulatory strategy globally and manage the required resources to meet an aggressive regulatory submission schedule, ensuring the effective fulfillment of company goals and objectives.  This will be an individual contributor role reporting to Sr. VP, Regulat...

• San Francisco
• $90,000 - $120,000
• Posted 5 months ago

POSITION SUMMARY The Sr. CTA acts as a central contact for the designated clinical study team and in this key support role supports the team in the planning, implementation, and completion of clinical studies both outsourced or in-house, through interaction with investigative sites, vendors, and ...

• San Francisco
• $110,000 - $120,000
• Posted 5 months ago

POSITION SUMMARY The Senior Clinical Research Associate (Sr CRA) will independently manage all clinical aspects of a small to medium-sized clinical study or, with supervision, assume significant management responsibilities on a large-scale study. This position works closely with a cross-functiona...

• San Francisco
• $160,000 - $190,000
• Posted 5 months ago

Sr. Clinical Trial Manager San Francisco, California POSITION SUMMARY Seeking a highly motivated Senior Clinical Trial Manager (Sr. CTM) to be a part of our Clinical Operations team. This is a unique opportunity to join a growing company committed to converting biologics and peptides into life-ch...

• San Diego
• $167,000.00-$241,925.00
• Posted 7 months ago

Responsible for contributing to the strategy and execution of regulatory CMC plans for emerging gene therapy portfolio. Will require relocation to Southern California with primarily onsite working policy. Your Role Responsible for the regulatory CMC strategy and execution for assigned commercial ...