- Takeda Pharmaceuticals (Boston, MA)
- …supplement experience requirements. + 6+ years' experience in pharmaceutical industry and/or clinical research organization, including 4+ years clinical ... empower you to shine? Join us as a Lead Clinical Study Manager based remotely reporting to...+ Knowledge in global regulatory and compliance requirements for clinical research , including but not limited to… more
- Abbott (Maple Grove, MN)
- …Writers and Reviewers). + Provide strategic guidance on regulatory requirements pertaining to clinical data and clinical evaluation to new product ... in more than 160 countries. The function of a Clinical Evaluation Project Manager supporting our Structural...and MDR submissions + 3-5+ years of experience in clinical research , quality systems, or regulatory experience… more
- Actalent (Waltham, MA)
- …trial management, project management, and vendor management. + 7-10+ years of clinical research experience in pharmaceutical/biotech or CRO settings. + ... Job Title: Senior Clinical Trial Manager Job Description Join...and forecasting. + Monitor study status and timelines, providing data for performance metrics reporting. + Work with the… more
- GRAIL (Menlo Park, CA)
- …development of completion guidelines, and other related activities, supporting study requirements and data quality. + Oversees clinical data entry progress ... For more information, please visit grail.com . The Sr. Clinical Trial Manager serves as a ...terms + Partners with cross functional stakeholders such as Clinical Data Management, Biospecimen Management, Finance, … more
- Actalent (Warren, NJ)
- As a Senior Manager Clinical Study Lead in Experimental Sciences, you will lead a cross-functional study team responsible for the delivery of clinical ... team for clinical study delivery. + Provide operational input into research plan and study protocol development. + Ensure timely completion of study-specific… more
- City of New York (New York, NY)
- …District Health Officers. This bureau will support programming, planning and research opportunities to address racial inequities resulting in premature mortality in ... oversight of the New York Coalition for Doula Access (NYCDA). The Doula Program Manager will be responsible for the following: DUTIES WILL INCLUDE BUT NOT BE LIMITED… more
- Regeneron Pharmaceuticals (Armonk, NY)
- …ICH/GCP. This role applies to internally sourced studies and studies out-sourced to Clinical Research Organizations (CROs) and the balance of direct leadership ... for respective clinical studies + Demonstrates expert knowledge and a data driven approach to planning, executing, and problem solving + Advanced communication… more
- ThermoFisher Scientific (Austin, TX)
- …project specifications. Provides trial status tracking and progress update reports to the Clinical Team Manager (CTM) as required. Ensures study systems are ... actions to bring the site into compliance and decrease risks. Ensures data accuracy through SDR, SDV and CRF review as applicable through on-site… more
- ThermoFisher Scientific (Chicago, IL)
- …project specifications. Provides trial status tracking and progress update reports to the Clinical Team Manager (CTM) as required. Ensures study systems are ... actions to bring the site into compliance and decrease risks. Ensures data accuracy through SDR, SDV and CRF review as applicable through on-site… more
- Abbott (Santa Clara, CA)
- …Degree, RN, PharmD, PhD, or MD preferred. + 5-7+ years of experience in clinical research , clinical affairs, regulatory affairs, or quality systems, in ... from routine fingersticks. The Opportunity The primary function of a **SENIOR CLINICAL EVALUATION SCIENTIST/PROJECT MANAGER ** is to combine understanding of… more