- Tris Pharma (Monmouth Junction, NJ)
- …Monmouth Junction, NJ facility for an experienced MD to serve as Senior Director or Director , Clinical Development. Title and salary commensurate with ... and company clinical programs. ESSENTIAL FUNCTIONS Responsible for generation of key study documents and medical oversight of clinical study conduct;… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …clinical trials; 2) provide input on biomarker related sections of clinical study protocols and ensure instructions on sample collection, processing and shipping ... overseeing the establishment of biomarker assays at CROs in a GLP , GLP -like or CLIA environment.Experience and expertise in spatial platforms (eg mIHC,… more
- Genmab (Princeton, NJ)
- …peer review of pre-clinical toxicology studies , including tissue cross reactivity studies , investigative and GLP studies . Provide internal expertise to ... understand the mechanisms of toxicity observed non-clinically or clinically in order to help design mitigation strategies and minimize risk to patients. Contribute with evaluation, and implementation of new technologies and techniques for tissue-based assays… more
- CTG (Pleasanton, CA)
- **Description** CTG is seeking to fill a ** GLP Study Director ** opening for our client in Pleasanton CA. **Duration: 3 months, with the potential to extend** ... **Location: Pleasanton, CA** **Overview:** As GLP Study Director , you will...will have overall responsibility for the technical conduct of GLP studies . You would be the principal… more
- Merck (West Point, PA)
- …a Toxicologist to conduct and/or monitor toxicity studies ( GLP and non- GLP ) as a Study Director or Study Monitor and to potentially serve as a ... drug candidates. **Key Responsibilities** + Serve as the single point of control ( Study Director ) on assigned acute through chronic general toxicology studies… more
- ManpowerGroup (Indianapolis, IN)
- …**Shift:** Monday to Friday (8:00 am - 5:00 pm) **Key Responsibilities:** + Maintain GLP instrumentation under study director 's guidance. + Manage liquid and ... + Perform combustion analysis and document data according to SOPs and GLP requirements. + Ensure compliance with laboratory safety procedures and regulatory… more
- Element Materials Technology (Eagan, MN)
- **Overview** Element-Eagan is hiring a ** Study Director ** to work in a fast-paced environment directing laboratory-based chemistry studies evaluating ... This is a 100% on-site position. **Responsibilities** + Perform Study Director functions, as outlined in EPA...interpretation of test assays to ensure technical integrity of studies + Perform study protocol review, raw… more
- Alaka'ina Foundation Family of Companies (Fort Detrick, MD)
- Molecular Virology Associate Study Director Location MD - Fort Detrick Job Code 12054 # of openings 1 Apply Now ... Foundation Family of Companies (FOCs) is looking for a Molecular Virology Associate Study Director to support our government customer located in Ft Detrick,… more
- Lilly (Indianapolis, IN)
- …monitoring of study conduct at the TPO via communication with the Study Director and/or onsite observation, and real time communication with the Toxicology ... conduct, including the fundamentals of Good Laboratory Practices ( GLP ) and data interpretation of nonclinical toxicology studies...report comments and assure they are conveyed to the Study Director at the TPO **Business Plan… more
- Charles River Laboratories (Mattawan, MI)
- …203Pb, etc. Utilizing these platforms/assays, the team is for execution of preclinical studies in small and large animal models in both regulated and non regulated ... preclinical studies . **Job Qualifications** **Knowledge, Experience, Skills and Abilities** required...discovery and safety assessment services, both Good Laboratory Practice ( GLP ) and non- GLP , to support clients from… more
- UTMB Health (Galveston, TX)
- …infectious diseases at BSL3 or higher levels of biocontainment. + Previously served as a Study Director on regulated studies , preferably for FDA Animal Rule ... Director for the Institutional Office of Regulated Nonclinical Studies (ORNcS), study sponsors and/or funding agencies...and/or funding agencies to design and execute regulated nonclinical studies compliant with the US FDA GLP … more
- HistoWiz (Long Island City, NY)
- …training files, master schedule, etc. + Lead internal audits in support of GLP studies , writing inspection reports, following up on observations, ensure timely ... customers' growing histology needs. Who are you? The Senior Manager/ Director of Quality is responsible for overseeing the quality...taken on any findings. + Prepare QA statements for GLP study reports. + Prepare laboratory and… more
- Charles River Laboratories (Skokie, IL)
- …and education are added correctly. **Job Summary** BASIC SUMMARY: The Associate Director , Immunoassay is responsible for the scientific and regulatory integrity of ... studies tested at the Charles River, Skokie site. This...state of art practices. + Provide scientific oversight of study design, preparation of protocols, interpretation and reporting of… more
- Charles River Laboratories (Ashland, OH)
- …involved in the conduct, direction, and execution of Bioanalytical Chemistry studies . Provide scientific direction, oversight, and guidance to staff. Maintain and ... processes and procedures to provide high quality standards of study design and timely reporting. Contribute to new business...* Ensure departmental policies, practices and procedures adhere to GLP /FDA regulations as they relate to the conduct of… more
- Orchard Therapeutics (Boston, MA)
- …its global headquarters in London and US headquarters in Boston. The Director , Bioanalytical Diagnostic Development, will be responsible for defining the global ... clinical bioassays/diagnostics, from preparations for 'first in human' up to registrational studies and post-approval commitments. As a key member of the Clinical… more
- Battelle Memorial Institute (West Jefferson, OH)
- …the development while maintaining quality and compliance. The Toxicologist functions as a study director within the organization and has oversight of the ... is located in **West Jefferson, OH.** **Responsibilities** + Serves as Study Director on toxicology, biodistribution, pharmacokinetic, efficacy, and related… more
- Battelle Memorial Institute (Columbus, OH)
- …Toxicologist functions as a subject matter expert within the organization and, as a study director , has oversight of the scientific elements of projects to ... findings, are accurately recorded and verified. + Identifies and incorporates exceptions to GLP conduct into GLP study Observes appropriate safety and… more
- Amgen (Washington, DC)
- …worldwide. It's time for a career you can be proud of. **Senior Director , Translational Safety and Bioanalytical Sciences - PTR Team Leader** **Live** **What you ... and Bioanalytical Sciences (TS&BA) function is actively seeking a **Senior Director ** to join the Leadership Team overseeing the Portfolio Scientific Leadership… more
- Charles River Laboratories (Wilmington, MA)
- …and production across global business units. It will directly assist the Executive Director (ED) in their responsibilities of assessing animal welfare risk and in ... Course, national AALAS meetings. + Participate in in-house animal welfare-related studies and information-sharing to determine best practices. + Prepare supporting… more
- Frontier Medicines (South San Francisco, CA)
- …Management of drug substance process chemistry development, scale up, and manufacturing for GLP studies and GMP manufacturing at CDMOs + Develop manufacturing ... Medicines is seeking a highly motivated individual for a newly created Associate Director role in Process Chemistry in Frontier's South San Francisco office. The… more
