Life Sciences jobs

• Silver Spring
• Commensurate based on experience
• Posted 6 days ago

Position Title: Site Lead (Director/VP) Job Type: Full time Onsite 5 days a week Company Background: Our company is a pioneering organization specializing in drug-eluting biomatrix products, designed to offer physicians the benefits of natural biological materials combined with targeted therapeut...

• Stamford
• $200,000 - 240,000
• Posted 12 days ago

The Regulatory Affairs Labeling Director will serve as an expert resource for regulatory labeling and will lead the successful development and implementation of labeling for the company.  Location – Remote: Essential Duties And Responsibilities   Create and maintain labeling content for marketed ...

• Lakewood
• 90,000
• Posted 19 days ago

Job Title: Validation Engineer II Location: Onsite in Lakewood, NJ Monday through Friday Compensation: $89,000-$92,000 DOE   Overview: The Validation Engineer II is responsible for duties associated with qualifying manufacturing and packaging equipment and Pharmaceutical utilities, including: HVA...

• San Diego
• $167,000.00-$241,925.00
• Posted about 2 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 ...

• Lakewood
• 125,000
• Posted 2 months ago

Job Title: Validation Supervisor Location: Lakewood, NJ Status: Full time direct hire Compensation: $115,000 to $130,000 depending on experience Please note, this position is not able to provide visa transfer, or sponsorship. Overview: This position is responsible for equipment, critical utilitie...

• Massachusetts
• $285,000-$325,000
• Posted 2 months ago

Senior Medical Director/Global Safety Officer - Drug Safety and Pharmacovigilance  Job Overview:  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 p...

• South San Francisco
• $320,000-$335,000
• Posted 3 months ago

The Director of Clinical Development will support early to late-stage clinical studies across multiple indications and build and develop strong working relationships with Principal Investigators and study sites to optimize study conduct and position the Company as a true partner of choice in the ...

• San Francisco
• $215,000 - $280,000
• Posted 3 months 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...

• Lakewood
• $75,000
• Posted 3 months ago

Job Title: Production Planner- CDMO Location: Lakewood, NJ Compensation: $75,000- $80,000 per year.   The Production Planner is responsible for developing and optimizing production plans that align with company goals, client demand, capacity constraints and ensures efficient utilization of resour...

• Boston
• $180,000-215,000
• Posted 4 months 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 4 months 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 4 months 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 4 months 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...

• San Francisco
• $260,000-$280,000
• Posted 4 months ago

Responsibilities Build and lead the medical writing department by managing internal and external medical writers and assessing resource needs to meet the organizational goals. Establish key document development processes, standards and style guides in collaboration with a cross-functional team. P...

• Boston
• $200,000-$260,000
• Posted 5 months ago

Director/Senior Director, Biostatistics Summary In this new role, reporting to the Vice President, Biometrics you will be working with cross?functional clinical teams responsible for statistical activities across clinical programs, including overseeing statistical deliverables outsourced to clini...

• San Carlos
• TBA. Estimated range: 200-235K base
• Posted 5 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...

• San Carlos
• $190,000-235,000
• Posted 5 months ago

Director, Portfolio Management Location: San Mateo, CA Position Overview: This role involves overseeing portfolio operations for development programs, managing cross-functional teams, and ensuring alignment with strategic goals. Key responsibilities include driving strategic planning, assessing o...

• Emeryville
• $150,000-200,000
• Posted 5 months ago

Senior Data Scientist Location: Emeryville, CA Company Overview: A clinical-stage biopharmaceutical company focused on developing innovative cell therapies. Role Summary: Collaborate with cross-functional teams to develop and integrate tools for data visualization, analysis, and exploration. Supp...

• Emeryville
• $184,000-260,000
• Posted 5 months ago

Director, Clinical Data Management Location: Emeryville, CA Company Overview: A clinical-stage biopharmaceutical company developing innovative cell therapies. Role Summary: Lead and manage the Clinical Data Management team, overseeing all aspects of data management for clinical development progra...

• Emeryville
• $240,000-300,000
• Posted 5 months ago

Senior Director, Biostatistics Location: Emeryville, CA Company Overview: A clinical-stage biopharmaceutical company focused on developing cell therapies using advanced T cell engineering. Role Summary: Lead the Biostatistics team, collaborating with stakeholders and CROs to oversee and support c...