NetSource, Inc.
- Raritan, NJ
- Posted today
Skills: Microbiology Experience, Water Sampling, GMP Environment Please note this is a 10-month contract position. Performs routine bioburden and endotoxin testing. Performs water sampling and environmental monitoring of the manufacturing areas. Supports validation testing as necessary. Reads and interprets test results and elevates issues to management in a timely manner. Good communication skill
Bristol-Myers Squibb
- Princeton, NJ, 08540
- Posted today
Scientific & Technical Expertise Required: • Accountable for all Immunoscience DMCP pre-DP4.5 assets and associated clinical studies • Leads a team of clinical professionals for Immunoscience areas in the planning, execution, and interpretation of data for phase I-II human clinical trials and discovery medicine/mechanism of action studies • Provides strategic leadership and oversight for the clini
Bristol-Myers Squibb
- Princeton, NJ, 08540
- Posted today
Clinical development lead for Nulojix (belatacept), reporting to the Vice-President of GCR Immunology. As a key scientific and clinical leader for the product serves as a core member of the full development team and oversees medical directors and study directors on the project. Strategically creates the overall clinical plan for the program by soliciting and integrating input from statistics, regu
Bristol-Myers Squibb
- Princeton, NJ, 08540
- Posted today
-Leads and participates in cross-functional oncology drug development matrix teams. -Designs and develops proof-of-concept research plans, develops Phase I/II and clinical pharmacology protocols. -Leads the execution of clinical studies and interpretation of data and makes appropriate recommendations based on these data. -Serves as a medical and scientific expert to drug discovery teams and contri
CorePharma, LLC
- Middlesex, NJ, 08846
- Posted today
JOB SUMMARY: Under minimum supervision, manage R&D projects from inception through technology transfer. Types of projects include but not limited to Alternate Source API and ANDA new product developments/filings. Develop project plans to facilitate successful project completions. Manage and drive project activities including project planning, internal/external communications, project task assignme
Ivory Systems
- Basking Ridge, NJ, 07920
- Posted today
We are looking for several Drug Safety Specialists for long term contracts. Positions can be either salaried with benefits and vacation or hourly. RESPONSIBILITIES: Evaluating, investigating and computerizing Adverse Events Case Reports. REQUIREMENTS: 2-5 years of Drug Safety experience BS Degree, RN preferred strong work ethic pharmacovigilance knowledge
Joule Scientific
- Somerville, NJ
- Posted today
Currently we have a temporary opening for a Research Scientist- Clinical Pharmacology to support a company located in the Somerville, NJ area. Responsibilities: Responsible for the performance of all aspects of clinical sample pharmacokinetic and immunogenicity analysis. Will assess product drug levels and immunogenicity in patients using a variety of analytical procedures including ELISA, Biacore
Bristol-Myers Squibb
- Princeton, NJ, 08540
- Posted today
Pivotal member of the Oncology YERVOY Home Office Medical team in developing and implementing programs that support YERVOY, including the development of the Medical and the Post Marketing Trial Plans and coordinating their implementation across the Medical Affairs functional matrix including clinical trials, medical liaisons, medical information, outcomes research, etc. Areas of responsibility inc
Bristol-Myers Squibb
- Princeton, NJ, 08540
- Posted today
Be key scientific and clinical leader for a product within internal and external forums, is responsible for internal and external scientific presentations related to the compound. Strategically solicit and integrate input from statistics, regulatory, outcomes research, marketing and other experts. Creates the overall clinical plan, considers new and novel approaches to study design or execution th
Smith Hanley Consulting Group
- Bridgewater, NJ, 08807
- Posted today
Title of Position: Drug Safety Data Management Specialist Location: Bridgewater, New Jersey Zip code: 08807 All work to be performed onsite in Bridgewater, NJ REQUIRED: · BA degree REQUIRED. · Regulatory Documentation experience related to the safety side is required. · Must HAVE Clinical Drug Safety experience. JOB DESCRIPTION: · Book-in and data enter information into the global safety database
Integrated Resources, Inc.
- Bridgewater, NJ, 08817
- Posted today
Drug Safety Specialist Location: Bridgewater, NJ Job Type: Full-Time Duration: 1 year contract Days: Flexible (5 days a week) Hours: Flexible (40hrs/week) Job Description · Book-in and data enter information into the global safety database for initial or follow up cases received via paper, fax or email. · Accept E2B cases received through the Argus Electronic Submissions Module (ESM) from license
MedFocus LLC
- Montville, NJ
- Posted today
• Responsible for the production of non-CRF data collection specification documentation • Defines the study specific non-CRF data handling strategy • Collaborates with SMT to agree on vendor expectations for the collection and transfer of data • Reviews and refines the technical requirements with service provider to establish the transfer of non-CRF data • Responsible for establishing appropriate
ABS Inc.
- Multiple locations
- Posted today
Cell Culture Lab Tech Positions are available in Wilmington, DE and approximately 20 miles North of Philadelphia, PA. ABS Inc. (www.absbio.com) is a successful bioscience company with nearly 21 years’ experience providing cell culture and other services for R&D to pharmaceutical and biotechnology clients worldwide. Experience in mammalian cell culture with a BS, BA, or higher degree is essential.