- Eclaro (North Plainfield, NJ)
- …rewarding opportunity! Position Overview: We are seeking a highly motivated and detail-oriented US Medical Scientist Associate to join our medical ... Scientist Associate Job Number: 24-03333 Be... Scientist Associate Job Number: 24-03333 Be part of a...play a critical role in executing the targeted therapies medical strategy including promotional review. This position requires a… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Associate Principal Scientist , General Medicine Publications Medical Writing, works with scientists in our company's Research Labs and ... development projects and other of our Research & Development Division science. The Associate Principal Scientist is expected to collaborate with our Research &… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... complexity in design and geographic scope). Prepares clinical section of regulatory document. Collaborates as team member with AROs/CROs. Drafts development plans,… more
- Merck & Co. (Rahway, NJ)
- …their knowledge of product and process development in the (bio)pharmaceutical and/or medical device industries to set tactical and strategic direction on programs ... products and processes are developed in accordance with applicable regulatory , quality, company, and customer requirements.-This position will lead cross-functional… more
- Merck & Co. (North Wales, PA)
- …state-of-the art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and ... the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.The incumbent is responsible for… more
- Merck & Co. (Rahway, NJ)
- …a cross-functional Senior/ Executive Director group of experts in commercialization, regulatory affairs, statistics, medical affairs and manufacturing to manage ... teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs and new indications for existing products. We… more
- System One (Rahway, NJ)
- Job Title: Associate Principal Scientist , Regulatory Affairs Location: Rahway, NJ (Hybrid) Hours/Schedule: Mon- Fri; 8am- 5pm Type: Contract Responsibilities ... The Associate Principal Scientist is responsible for developing CMC regulatory ...eligible employees health and welfare benefits coverage options, including medical , dental, vision, spending accounts, life insurance, voluntary plans,… more
- Organon & Co. (Plymouth Meeting, PA)
- …in Organon Regulatory Chemistry, Manufacturing and Controls New Products, the Associate Principal Scientist ( Associate Director) is responsible for ... and will encompass late-stage development products and commercially approved compounds. The Associate Principal Scientist may also support project team goals and… more
- J&J Family of Companies (Spring House, PA)
- …to patients with immune-mediated diseases. Position Overview: The focus of the Associate Director Clinical Scientist is to support various clinical research ... be found. Johnson & Johnson discovers and develops innovative medical solutions to address important unmet medical ...depending on the therapeutic area and trial-specific requirements. The Associate Director Clinical Scientist is a key… more
- Merck (Rahway, NJ)
- **Job Description** The Associate Principal Scientist , General Medicine Publications Medical Writing, works with scientists in our company's Research Labs ... development projects and other of our Research & Development Division science. The Associate Principal Scientist is expected to collaborate with our Research &… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- We are seeking an Associate Director to join out Oncology Clinical Development department. The Associate Director Clinical Sciences leads in the development, ... of study data of a clinical development program. The Associate Director leads in a matrix environment as part...to the Director, Clinical Sciences and collaborates closely with Medical Director(s) (MDs) to provide scientific expertise necessary to… more
- Bristol Myers Squibb (San Diego, CA)
- …some of the brightest minds in biopharma. **Position Summary:** The Senior Associate Scientist is a laboratory-based, integral member of the Neuroscience ... with a high probability of success to address unmet medical needs; Targets in neuromuscular diseases. Use approaches in...in vivo experience would be considered advantageous. The Senior Associate Scientist will also be in a… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- The Associate Director, Clinical Sciences contributes to the development, evaluation, planning and execution of hematology clinical studies and ensures scientific ... Director, Clinical Sciences Hematology, Clinical Sciences and collaborates closely with Medical Director(s) (MDs) to provide scientific expertise necessary to design… more
- dsm-firmenich (Exton, PA)
- **Analytical Associate Scientist ** **Exton, PA** The Analytical Associate Scientist will assure that dsm-firmenich Biomedical products are of consistent ... for duties related to the research, development, testing and manufacturing of medical device materials, products or technologies in compliance with GMP and ISO… more
- Catalent Pharma Solutions (Kansas City, MO)
- ** Associate Scientist II, Biologics I - Analytical Chemistry** **Position Summary:** Catalent, Inc. is a leading global contract development and manufacturing ... Pharma Solutions in Kansas City, MO is hiring an Associate Scientist II, Biologics I who is...testing samples, drafting methods and reporting data under cGMP regulatory guidance for Large Molecules/Biologics product development and related… more
- University of Miami (Miami, FL)
- …of Pulmonary, Critical Care, and Sleep Medicine has an exciting opportunity for an Associate Scientist . The Associate Scientist contributes to basic ... animals, ensuring their welfare and compliance with ethical guidelines and regulatory requirements. + Maintain laboratory cleanliness and orderliness, including the… more
- Actalent (Gaithersburg, MD)
- Job Title: Associate Scientist , Analytical Development Protein BiochemistryJob Description We are seeking an Associate Scientist Contractor to join our ... analyze, and document analytical data generated in support of regulatory requirements. + Good understanding of statistical tools and...for this temporary role may include the following: - Medical , dental & vision - Critical Illness, Accident, and… more
- Eurofins (Columbia, MO)
- …purity of biological substances and products. Eurofins BPT-Columbia is looking for an Associate Scientist to join our Biochemistry team located in Columbia, ... Missouri. The Associate Scientist position is an entry-level professional...etc. Reports data in a timely manner according to regulatory guidelines and other governing rules or regulations. Assists… more
- Eurofins (Columbia, MO)
- …substances and products. Job Summary: Eurofins BPT-Columbia is looking for an Associate Scientist to join our Biochemistry Method Development and Validation ... team located in Columbia, Missouri. The Associate Scientist position is an entry-level professional...Follow cGMP processes and procedures and adhere to all regulatory requirements + Run a variety of equipment including… more
- Amgen (Rockville, MD)
- …us and transform the lives of patients while transforming your career. Process Development Associate Scientist **What you will do** Let's do this. Let's change ... to rapidly solve day-to-day experimental challenges. Additionally, the Process Development Associate Scientist will utilize out-of-the-box thinking to contribute… more
