Life Sciences jobs

• San Francisco
• $215,000 - $280,000
• Posted 3 days 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 9 days 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 15 days 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 16 days 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 21 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 ...

• Lakewood
• 75,000
• Posted 22 days ago

Job Title: Deviations Investigator Location: Onsight Lakewood, NJ Salary: $70,000-$75,000 Overview: The purpose of this position is to serve as a primary investigator for the Operations Group to ensure timely and accurate completion of high-quality manufacturing investigations and implementation ...

• Cranbury
• 285000
• Posted about 1 month 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...

• Boston
• $180,000-$240,000
• Posted about 1 month ago

Position Overview: As the Associate Director / Director of Regulatory Strategy, you will play a critical role in driving the development and execution of regulatory strategies for our rare disease therapeutic programs. Your expertise and leadership will be instrumental in navigating the complex r...

• San Francisco
• $260,000-$280,000
• Posted about 1 month 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...

• Lakewood
• $94,000
• Posted about 1 month ago

Job Title: MS&T Scientist II Location: Lakewood, NJ Salary: $94,0000 Overview: The purpose of MST Scientist II position is to support the Company in the development and optimization of manufacturing processes, improving them and increasing the scale.  The ultimate goal is to develop processes tha...

• Redwood City
• $300,000-$340,000
• Posted about 2 months ago

Responsibilities: Charged with designing, developing and implementing the transition of the existing, clinically oriented functions toward a robust and reliable manufacturing and supply group, positioned to support global markets. In this, the organization must maintain its agile operational capa...

• Boston
• $200,000-$260,000
• Posted about 2 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 about 2 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 about 2 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 2 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 2 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 2 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...

• South San Francisco
• 230000
• Posted 2 months ago

Company Overview The Company’s lead product candidate has received Fast Track Designation and Orphan Drug Designation from the U.S. Food and Drug Administration for both idiopathic pulmonary fibrosis (IPF) and primary sclerosing cholangitis (PSC) and Orphan Drug Designation from the European Medi...

• Boston
• $180,000-$230,000
• Posted 2 months ago

AD/Director, Regulatory Operations & Affairs About the Role We are seeking a highly skilled, and experienced AD/Director of Regulatory to join our growing clinical team. This hands-on position will be responsible for overseeing and managing all global regulatory activities to ensure compliance wi...

• New Jersey
• $207,000.00 to $289,867.00 per year
• Posted 3 months ago

Overview Reporting to the Executive Director Quality GMP Compliance, the Director, Quality Operations will play a key role in managing QA oversight activities. He/she will be responsible for Quality related activities for commercial products including transition from development (Phase III) into ...