- Takeda Pharmaceuticals (Hagatna, GU)
- …is true to the best of my knowledge. **Job Description** **About the role:** ** Associate Director , Nonclinical Regulatory Writing and Submission ... to our inspiring, bold mission. As an Associate Director in the Nonclinical Regulatory Writing and Systems (NRWS) Department within Preclinical… more
- Bristol Myers Squibb (New Brunswick, NJ)
- …to management and development teams. + On an as-needed basis, interacts with regulatory agencies worldwide on issues of nonclinical safety evaluation. + Writes ... personal lives. Read more: careers.bms.com/working-with-us . This is a Hybrid role Nonclinical Safety (NCS), within Nonclinical Research and Biotherapeutics, is… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …other research areas centered around rare diseases and immune disorders. **Job Summary:** The Associate Director of Regulatory Writing is a key role ... planning and provide scientific and strategic insights at the study team level. The Associate Director of Regulatory Writing must possess advanced knowledge… more
- Novo Nordisk (Plainsboro, NJ)
- …across multiple functional areas. Relationships You will report to the Senior Director - Global Regulatory Portfolio Lead. Essential Functions + Serve ... plans to management and other internal stakeholders + Perform regulatory review of all clinical and nonclinical ...Perform regulatory review of all clinical and nonclinical documents for submissions, eg, clinical protocols and study… more
- AbbVie (Florham Park, NJ)
- …on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description Purpose: The Associate Director in CMC Statistics is responsible for providing statistical ... the planning/design, conduct, analysis, and interpretation of CMC studies and regulatory submissions. Participate in establishing departmental and nonclinical … more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- We are seeking a highly motivated ** Associate Director ** to join to our Bioanalytical Sciences team. You will be responsible for coordination of assay ... matter expert for external bioanalytical assay strategy and data interpretation. As an ** Associate Director ** , a typical day may include the following: +… more
- Bristol Myers Squibb (Princeton, NJ)
- …**Summary/Scope** Reporting to Senior Scientific Director Translational Medicine (TM), the TM Associate Director will be part of the late stage TM group. The ... + Works with TM laboratory scientists and academic TLs to address nonclinical translational questions + Participates in post-hoc biomarker analysis and publication… more
- Bristol Myers Squibb (Summit, NJ)
- …Join us and make a difference. **Summary/Scope** Reporting to Senior Scientific Director Translational Medicine, the TM Sr. Principal Scientist will be part of ... + Works with TM laboratory scientists and academic TLs to address nonclinical translational questions + Participates in post-hoc biomarker analysis and publication… more
- Merck (West Point, PA)
- **Job Description** The Nonclinical Drug Safety (NDS) division at our company is seeking a motivated Computational Biologist/Toxicologist for our Computational ... evaluations within and across multiple projects + Influence the regulatory toxicology landscape through active participation in external consortiums, publications,… more
- Haleon (Warren, NJ)
- …innovation and maintenance of business activities, by initially shadowing the Toxicology Associate Director /Sr. Toxicologist. This role will provide support to ... appropriate to generate toxicological data to derisk innovation programs. + Contribute to nonclinical CTD modules for regulatory submissions. + Keep up to date… more