Life Sciences jobs

• Rockville
• $210,000-275,000
• Posted 2 days ago

n/a

• Watertown
• $38 to $40 per hour
• Posted 4 days ago

Associate Formulation Scientist Status: 6 month contract Location: onsite in Watertown, MA Hourly rate: $38 to $40 depending on experience Position Summary The individual in this role will be part of an interdisciplinary team supporting pre-clinical and clinical programs through product design, r...

• Lexington
• $260,000-285,000
• Posted 16 days ago

Senior Director, Regulatory Affairs Greater Boston Description:  The Director/Senior Director, Regulatory Affairs is responsible for developing and executing the global regulatory strategy for the programs assigned. Reporting to the Head of Regulatory Affairs, this individual will develop and adv...

• San Diego
• $167,000.00-$241,925.00
• Posted 26 days ago

Responsible for contributing to the strategy and execution of regulatory CMC plans for assigned development and commercial projects leading to successful preparation and approval of IND/CTA/MAA/NDA/BLA submissions in a timely and efficient manner focused on development for biologics, small molecu...

• Lakewood
• 90,000
• Posted about 1 month ago

Title: Process Supervisor 3rd Shift Location: Lakewood, NJ Status: Full-time direct hire, onsite Experience: Minimum of 3 years experience and 1 year in a team lead or supervisor role. Compensation: $85,000 to $90,000 Shift: Sunday through Thursday 11pm to 7:30am   Description: Candidate will sup...

• Lakewood
• 125,000
• Posted about 1 month 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 about 1 month 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 about 2 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 2 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 2 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
• $34-$40 per hour
• Posted 3 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 3 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 3 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 3 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 3 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 3 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 4 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 4 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 4 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 4 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...