Life Sciences jobs

• Boston
• $55.00 an hour
• Posted about 7 hours ago

Title: Quality Assurance Associate 2md Shift Location: Lexington, MA Shift: 2nd Shift, 3 pm to 11pm Monday through Friday Status: 6-12 month contract Hourly rate: $55 an hour Quality Assurance Associate This individual in this office-based role will maintain on site quality presence at GMP facili...

• Massachusetts
• $285,000-$325,000
• Posted 4 days 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 19 days 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 about 1 month 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 about 1 month 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
• $34-$40 per hour
• Posted about 2 months ago

Lab Manager As a lab manager, you will play a critical role in supporting the smooth operation of our laboratory.  You will work in a highly dynamic research and development environment and will collaborate with scientists, information & technology, and facilities.  You will be responsible to ens...

• Boston
• $180,000-215,000
• Posted about 2 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 about 2 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 about 2 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 ...

• Lakewood
• 75,000
• Posted about 2 months 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 2 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...

• Boston
• $180,000-$240,000
• Posted 2 months 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 2 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...

• Lakewood
• $94,000
• Posted 3 months 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...

• Boston
• $200,000-$260,000
• Posted 3 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 3 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 3 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 3 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 3 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 3 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...