- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …of regulatory document. Collaborates as team member with AROs/CROs. Drafts development plans, protocol profiles, and sections of submission documents under guidance ... medical and/or scientific direction to Clinical Operations. Represents Clinical Development on Project Teams. ResponsibilitiesStudy Strategy: Provides the strategic… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …agencies. Supervise designated personnel. Relationships Report to the Director/ Associate Director/Lead Regulatory Scientist /Sr. Manager Regulatory Affairs. ... and collecting data to support efficacy and new product development , CMR is involved. The one thing that keeps...find better and more innovative ways to improve their quality of life. We're changing lives for a living.… more
- Bristol Myers Squibb (New Brunswick, NJ)
- …of analytical methods in support of solid oral and sterile drug product development and commercialization. The Associate Scientist will facilitate analytical ... analytical techniques of HPLC and Dissolution. Capillary Electrophoresis experience is a plus. ** Development Value:** + The Associate Scientist will have… more
- J&J Family of Companies (Raritan, NJ)
- Associate Director, Clinical Project Scientist (Oncology) - 2406181923W **Description** At Johnson & Johnson, we believe health is everything. Our strength in ... Learn more at https://www.jnj.com/ . Johnson & Johnson is recruiting for an Associate Director, Clinical Project Scientist , Oncology. The position can be located… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- The Associate Director, Clinical Scientist leads in the development , evaluation, planning and execution of hematology oncology clinical studies and ensures ... to manage one or more clinical scientists. As an Associate Director, a typical day may include the following:...Clinical Study Reports with minimal guidance and supports the development of regulatory documents; performs quality review… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- We are seeking a Associate Director to join out Oncology Clinical Development department. The Associate Director Clinical Sciences leads in the ... integrity and interpretation of study data of a clinical development program. The Associate Director leads in...Clinical Study Reports with minimal guidance and supports the development of regulatory documents; performs quality review… more
- Bristol Myers Squibb (Princeton, NJ)
- …resources, and milestones. Drafts the early safety strategy plan, the Early Development Safety Roadmap (EDSR). Authors safety data query responses, author and ... specific PV sections of the Periodic Benefit Risk Evaluation Report (PBRER), Development Safety Update Report (DSUR), and health authority (HA) submission documents… more
- Merck (Trenton, NJ)
- …to be one of the world's biggest investors in Research & Development . Employees within the Regulated PK/ADA Bioanalytical Outsourcing group provide oversight for ... outsourcing of regulated clinical and preclinical assay method development , validation, and sample testing in support of biologics and small-molecule programs. This… more
- Marriott (Trenton, NJ)
- …Type** Management **JOB SUMMARY** Applies advanced computational techniques in the development of business solutions to data-intensive problems in the hospitality ... applying analytical and programming skills against complex mathematical modeling and/or systems development + 1 year experience in software development including… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …of regulatory document. Collaborates as team member with AROs/CROs. Drafts development plans, protocol profiles, and sections of submission documents under guidance ... medical and/or scientific direction to Clinical Operations. Represents Clinical Development on Project Teams. **Responsibilities** + Study Strategy: Provides the… more
- ThermoFisher Scientific (New Brunswick, NJ)
- **Job Description** **Title: Labs FSP - Associate Research Scientist - Project Management** **Location: New Brunswick, NJ** This is a Monday** **-Friday position ... individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in… more
- Bristol Myers Squibb (Princeton, NJ)
- …every treatment we pioneer. Join us and make a difference. **Purpose** The Associate Director, Biostatistics is a core member of cross-functional development ... external partners, medical monitor, protocol manager, data manager, PK scientist , and other members of the study/indication team. **Primary Responsibilities**… more
- Novo Nordisk (Plainsboro, NJ)
- …agencies. Supervise designated personnel. Relationships Report to the Director/ Associate Director/Lead Regulatory Scientist /Sr. Manager Regulatory Affairs. ... and collecting data to support efficacy and new product development , CMR is involved. The one thing that keeps...find better and more innovative ways to improve their quality of life. We're changing lives for a living.… more
