- Novo Nordisk Inc. (West Lebanon, IN)
- …career. Are you ready to realize your potential? The PositionThe Deviation Investigator -Writer is responsible for investigating and writing of deviations to the ... merit and completeness according to regulatory expectations. The Deviation Investigator -Writer will be responsible for initiating investigations and writing… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …research areas centered around rare diseases and immune disorders. Summary: The Associate Director will lead the execution and lifecycle management of Global Medical ... on Harmonization (ICH) guidelines. This role emphasizes the management of Investigator Initiated Studies (IIS) and Collaborative External Sponsored Research (CESR)… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …research areas centered around rare diseases and immune disorders. Job Summary: The Associate Director of Regulatory Writing is a key role responsible for producing ... documents include, but are not limited to, clinical study reports, investigator brochures, regulatory briefing documents, and clinical and clinical pharmacology… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …other research areas centered around rare diseases and immune disorders.Summary The Associate Director of Regulatory Writing is a key role responsible for producing ... documents include, but are not limited to, clinical study reports, investigator brochures, regulatory briefing documents, and clinical and clinical pharmacology… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …for submissions, eg, clinical protocols and study reports, preclinical reports, investigator brochures, application summary documents, etc. Research and analyze the ... evolving competitive and regulatory landscapes to maintain current knowledge Effectively managing timelines while working in a fast-paced and dynamic environment across both time zones and cultures Physical Requirements 0-10% overnight travel required. Ability… more
- ORIC Pharmaceuticals, Inc. (San Diego, CA)
- …degree preferred.At least 8+ years of regulatory affairs experience for the associate director or 10+ years of Regulatory affairs experience for the director ... to collaborate on development of high-quality clinical-regulatory documents, eg, investigator brochures, meeting request/package.Strong organizational skills, with the ability… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …Global Safety Lead(s), Global Safety Lead(s) and Global Safety Scientist(s)/ Associate within Safety Surveillance. Essential Functions Innovation and change ... Development Plan (PDP), Trial Outline, Protocol, Clinical Trial Report, Investigator 's Brochure (IB), integrated safety summaries, abstracts and planned publications… more
- Daiichi Sankyo, Inc. (Nashville, TN)
- …and study committee members for DSI clinical research programs, 2) investigator -initiated research study proposals, 3) speakers for DSI Brand Speaker programs, ... in Oncology, clinical research and medical education preferred Principal MSL/ Associate Director MSLExperience Qualifications:5 or More Years' experience including… more
- Merck & Co. (North Wales, PA)
- Job DescriptionThe Associate Vice President, Global Data Management & Standards (GDMS) is responsible for ensuring that all clinical data management products and ... Sciences, BARDS, GCTO, R&D IT) and external (functional service providers, labs, investigator sites, etc.) stakeholders to deliver products and services supporting a… more
- Merck & Co. (Upper Gwynedd, PA)
- …They lead a team of TA dedicated global and regional directors and associate directors. The EDMA engages with global scientific leaders and key decision makers. ... coordinates local data generation studies (LDG) with ORSupports the Investigator -Initiated Study programLeads talent review process and demonstrates follow-through… more
- Enrs Go (Washington, DC)
- …nursing faculty , campus based, who is tenure eligible at the rank of Associate Professor or Full Professor, and shares a commitment to the mission, vision and ... state if not resident in Washington, DC Be eligible for rank at Associate /Full professor standing (tenure eligible) at Georgetown University Minimum 5 years of… more
- University of California - San Francisco (San Francisco, CA)
- …as the Executive Director of the California Poison Control System at the Assistant, Associate or Full Professor rank in the Health Sciences or Professor of Clinical ... of Clinical Pharmacy. The Executive Director serves as the Principle Investigator /Project Director for all CPCS Contracts and Grants following UCSF policies.… more
- University of California - Irvine (Irvine, CA)
- …and all ranks in the Professor of Clinical "X" Series (Assistant, Associate , In-Residence, and/or Full Professor levels). Duties will include clinical care, teaching ... funding. The Department participates in NRG/RTOG and SWOG and encourages investigator -initiated clinical and translational trials.Founded in 1965, the University of… more
- Daiichi Sankyo, Inc. (Boston, MA)
- …and study committee members for DSI clinical research programs, 2) investigator -initiated research study proposals, 3) speakers for DSI Brand Speaker programs, ... in Oncology, clinical research and medical education preferred. Principal MSL/ Associate Director MSL Experience Qualifications: 5 or More Years' experience… more
- Tufts University (Washington, DC)
- …Tufts is appointed by Tisch College of Civic Life and reports to the Associate Dean of Tisch College. Tufts University Schools of Medicine, Dental Medicine, and ... leverage resources across departments and partners to serve student and investigator needs. Prepare communications materials and present findings and accomplishments… more
- Merck (Honolulu, HI)
- …They lead a team of TA dedicated global and regional directors and associate directors. The EDMA engages with global scientific leaders and key decision makers. ... coordinates local data generation studies (LDG) with OR.Supports the Investigator -Initiated Study program.Leads talent review process and demonstrates follow-through… more
- Regeneron Pharmaceuticals, Inc (Sleepy Hollow, NY)
- …groups, advocacy groups, and other external collaborators.Prioritizing support of investigator -initiated studies and serving as a key member of internal ... annual goals and core business strategy.Potential to supervise Medical Directors and/or Associate Director.This may be for you if you:* Want to challenge the… more
- City of New York (New York, NY)
- …BE CONSIDERED FOR THIS POSITION CANDIDATE MUST BE SERVING PERMANENTLY IN THE TITLE OF ASSOCIATE INVESTIGATOR , OR REACHABLE ON THE ASSOCIATE INVESTIGATOR ... and five years of satisfactory, full-time experience as an investigator evaluating credit worthiness, searching for assets, verifying information concerning… more
- City of New York (New York, NY)
- …materials, in response to requests. The specific duties and responsibilities of an Associate Investigator assigned to the Legal Bureau's FOIL Unit will include: ... and five years of satisfactory, full-time experience as an investigator evaluating credit worthiness, searching for assets, verifying information concerning… more
- City of New York (New York, NY)
- …of reports that will go before trials and hearings. The responsibilities of the Associate Investigator will include but not be limited to: - Investigate ... and five years of satisfactory, full-time experience as an investigator evaluating credit worthiness, searching for assets, verifying information concerning… more
