- Novo Nordisk (Princeton, NJ)
- …The Position The Associate Director is an expert in medical writing and performs work independently with minimal-to-no supervision. The Associate ... input into development plans, study designs, and regulatory submissions. Relationships The Associate Director , Medical Writing (ADMW) reports to a … 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 ... Clinical Sciences Hematology, Clinical Sciences and collaborates closely with Medical Director (s) (MDs) to provide scientific expertise...to manage one or more clinical scientists. As an Associate Director , a typical day may include… more
- J&J Family of Companies (Raritan, NJ)
- Associate Director , Autologous Cell Therapy Process Development - 2406176241W **Description** Johnson & Johnson is currently seeking an Associate Director ... We are seeking an energetic and highly motivated candidate for the role of Associate Director , who possesses proven expertise in autologous cell therapy process… more
- J&J Family of Companies (Titusville, NJ)
- Associate Director , Global Labeling Product Leader (1 of 2) - 2406187352W **Description** Johnson & Johnson Innovative Medicine is recruiting for an Associate ... Relevant experience in the pharmaceutical industry (eg, Regulatory Affairs, Clinical, Medical Information, Pharmacovigilance) including at least 6 years of direct… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- We are looking for an Associate Director , within our Clinical Pharmacology group. Providing strategic and scientific expertise, as well as representing Clinical ... or Boston,MA location.** **A day in the life an Associate Director may look like:** + Develop...clinical pharmacology study reports and publications. Work with the Medical Writing Team to incorporate PK/PD sections… more
- System One (Basking Ridge, NJ)
- Job Title: Associate Director , Biostatistics Client - Global Pharmaceutical Company Location: Remote, US Based only - must reside in EST or CST time zones Type: ... Health Authorities globally by providing input for the interaction or by writing the interaction document. May participate in meeting or teleconferences with Health… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …other research areas centered around rare diseases and immune disorders. **Summary** The Associate Director , Privacy & Compliance Investigations, is a member of ... pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... and guidelines, reviews and provides written assessments of relevant medical topics, and supports PV Operations' medical ...team members. + Reports and Submissions: May contribute to writing minor safety sections of the NDA, CSR, and… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …implementation of sourcing strategies for a specific set of R&D categories (CRO, Medical Writing , BDM, etc..). Builds strategic plans for specific categories ... pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and… more
- Bristol Myers Squibb (Princeton, NJ)
- …resources; ensure appropriate quality controls in place for compliant submissions + Writing regulatory documents (eg new INDs, briefing book content, BT Designation ... a strong, collaborative relationship with all key stakeholders including Commercial, Medical Affairs, Promotion & Compliance, Global Development, and other functions… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... Health Authorities globally by providing input for the interaction or by writing the interaction document. May participate in meeting or teleconferences with Health… more
- CenterWell (Trenton, NJ)
- …a part of our caring community and help us put health first** **National** ** Director of Transitional Care and High-Risk Patient Management** The Director of ... Computer skills in word processing, database management, spreadsheets, and report writing . * Proficiency in tracking and evaluating process/system outcomes and… more
- Boehringer Ingelheim (North Brunswick, NJ)
- **Description** The Associate Director , Bioanalysis is responsible for providing expertise in the areas of Ligand binding assay method development and sample ... Independently develop method and performing sample analysis without supervision, act as study director , report writing and participate in method demo and method… more
- University of Pennsylvania (Philadelphia, PA)
- …(CRU)- Myeloma Research Team and indirectly report to the CRU Central - Associate Director of Clinical Research Operations. The successful candidate will work ... and quality of research. + The candidate will work closely with the CRU Associate Director of Operations to develop and implement SOP's, report team study… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …role is primarily a tactical study delivery role, reporting into an Associate Director or above responsible for Operational Study Strategy. **Responsibilities:** ... & coordination role for the protocol and amendments. Additional medical writing tasks may involve ICF, CRF...university) + Bachelor's Degree in the Sciences preferred + Associate 's degree or with a nursing diploma with substantial… more
- Highmark Health (Trenton, NJ)
- …case and disease management identification process, and consult with the Organization's Associate Medical Directors and Medical Directors when appropriate, ... FDA-approvals and drug manufacturer pipelines, assessing drug utilization reports, and writing drug monographs for Pharmacy & Therapeutics Committee review. + Assist… more