- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …immune disorders. Summary Drafts development plans, protocol profile, protocol, and clinical sections of submission documents under guidance of CSL and/or Medical ... Monitor. Represents Clinical Development on Study Team and collaborates as team...with other functions, ARO, CRO. Provides scientific input to Clinical Operations and other functions. This position provides critical… more
- Merck & Co. (North Wales, PA)
- …execution of clinical protocol(s). This may include:Serving as the lead clinical scientist on a clinical trial team.Leading medical monitoring ... Summary: This position leads the scientific planning and execution of one or more clinical trials or significant aspects thereof. In this position, you will have the… more
- Merck & Co. (North Wales, PA)
- …the clinical /scientific execution of clinical protocol(s).Serves as the lead clinical scientist on the clinical trial team.Collaborates with the ... Medical Writer on clinical /scientific and regulatory documents.Partners with Study Manager on study deliverables.Participates in the set up and design during… more
- Merck & Co. (North Wales, PA)
- Job DescriptionDescription: The Associate Principal Scientist , Oncology Publications Medical Writing, works with scientists in our company's Research Labs and ... and posters/oral presentations that report results from our company oncology clinical trial program, as well as select early-stage development projects and… more
- Aequor (South San Francisco, CA)
- …(SHORTLISTED, REJECTED JOB SEEKERS from prior request AMAGJP00012397) OPEN MARKET RATE - Hiring Manager has budget up to /hour Max for the hourly bill rate ( /hour ... work for 45min. The Computational Biology group in the Clinical Biomarkers & Diagnostics (CBD) department at is seeking...department at is seeking a highly motivated Sr data scientist to join our team and contribute to develop… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …designated personnel. Relationships Report to the Director/Associate Director/Lead Regulatory Scientist /Sr. Manager Regulatory Affairs. Develop and maintain ... About the Department The Clinical , Medical and Regulatory (CMR) department at Novo...Essential Functions Compile and submit responses to FDA communications. MANAGER , THERAPEUTIC AREA: Compile, submit and maintain applications (IND,… more
- Merck & Co. (North Wales, PA)
- …and adaptations, dossiers, other activities in support of HTA, and publications.- Supports Scientist (s) in V&I Outcomes Research, V&I GMSA, BARDS HEDS, and others as ... and Skills:Required:Three or more years of work experience within clinical /observational research or equivalent-Excellent communication and interpersonal skills; ability… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- The Senior Manager , Hematology, Clinical Scientist leads in the development, evaluation, planning and execution of clinical studies and ensures integrity ... and interpretation of study data of a clinical development program. The Sr. Manager leads in a matrix environment as part of a cross-functional team and may… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …immune disorders. Summary Drafts development plans, protocol profile, protocol, and clinical sections of submission documents under guidance of CSL and/or Medical ... Monitor. Represents Clinical Development on Study Team and collaborates as team...with other functions, ARO, CRO. Provides scientific input to Clinical Operations and other functions. This position provides critical… more
- Abbott (Maple Grove, MN)
- …Clara, CA or Maple Grove, MN currently has an opportunity for an on-site **Senior** ** Clinical Scientist /Project Manager Clinical Evaluation** . This new ... provide guidance, and oversight of CER Medical Writers' development of Clinical Evaluation Reports and associated documents; set deliverable and project timelines… more
