Life Sciences jobs

• Gaithersburg
• $200,000 - $250,000 a year
• Posted about 17 hours 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...

• Lakewood
• $110,000 to $1150,000
• Posted 6 days ago

Title: Laboratory Systems Supervisor Status: Full-time direct hire Location: Onsite Monday-Friday Compensation: $110,000 to $115,000 annual salary   The laboratory systems manager is responsible for creating and reviewing business processes, identifying and addressing operational functionality of...

• South San Francisco
• $80 - 120/Hour
• Posted 6 days 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...

• South San Francisco
• $100 - $150/hour
• Posted 6 days ago

GCP SOP Writer Contractor (20-30 hours/week) POSITION SUMMARY The GCP SOP writer is responsible for drafting, editing and performing quality control review of Clinical Operations procedures.  The candidate will work with process owners, subject matter experts and relevant stakeholders to develop ...

• South San Francisco
• $45 - $75/hour
• Posted 6 days ago

rial Master File (TMF) Manager Contractor POSITION SUMMARY The TMF Manager Contractor will support day-to-day management of Trial Master File (TMF) operations, including TMF projects, key performance indicators (KPIs), electronic TMF (eTMF) systems, vendor TMF activities, and functional subject m...

• Lakewood
• $120,000 to $140,000
• Posted 7 days ago

Job Title: Automation Engineer Location: US-NJ-Lakewood Compensation: $120,000 to $140,000 DOE   Overview: Individuals will be responsible for installing, maintaining, and troubleshooting the automation systems for automated utility, processing, filling, inspection, and packaging equipment.  The ...

• San Francisco
• $175000-190000
• Posted 11 days 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...

• Boston
• $300,000 - $350,000
• Posted 13 days ago

Key Responsibilities: Design and lead clinical development strategies for oncology programs (typically Phase I–II). Oversee study startup, site selection, vendor management (e.g., CROs, labs). Ensure trial timelines, budgets, and quality targets are met. Build and scale the Clinical Operations te...

• Waltham
• $320,000-$358,000
• Posted 14 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
• $260,000 - $310,000 a year
• Posted 21 days 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 about 1 month 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...

• Fishers
• $170,000-195,000
• Posted 2 months ago

n//a

• Gaithersburg
• Commensurate with experience
• Posted 3 months ago

Position Overview: This role is a critical position within the organization, focused on executing the company’s short-term production goals and objectives. The Manager of Production Manufacturing is responsible for overseeing departmental activities across all aspects of the tissue manufacturing ...

• Gaithersburg
• Commensurate with experience
• Posted 3 months ago

Manager, Quality Assurance and Quality Control Position Overview: This role is a key position within the organization, contributing to setting short- and medium-term goals related to quality assurance. The Manager of Quality Assurance & Quality Control is responsible for overseeing and maintainin...

• South San Francisco
• $190,000 - $215,000
• Posted 3 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...

• Boston
• 200,000-225,000 a year
• Posted 3 months ago

Job Title: Director Regulatory Affairs Strategy      Location:  Remote OR Menlo Park, CA OR Waltham, MA Position Overview: The Director Regulatory Affairs Strategy provides global regulatory oversight and project leadership of assigned development products and reports to the Vice President Regula...

• San Francisco
• $290,000 - $350,000
• Posted 3 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 3 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 3 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 3 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 ...