- Touro University (Valhalla, NY)
- …duration of each project . + Direct liaison between sponsors/investigators and the research coordinator or Vice President + Establish research data and work ... analytical study related protocols and documents, as well as research / clinical data analysis. + Manage the orders,...+ Drive internal communication, including timelines, budget, progress, and project needs for clinical trials to product… more
- Touro University (Valhalla, NY)
- …The candidate will report to Dr. Salomon Amar, VP for Research , and to the Clinical Research Project Manager . Incumbent will manage all aspects of ... + Contribute to the development and implementation of SOPs, project -specific procedures, budgets, and technical guidance documents. + Monitor, adherence… more
- Regeneron Pharmaceuticals (Armonk, NY)
- The ** Manager Clinical Study Lead** (CSL **)** may perform the following responsibilities with moderate oversight: accountable for the global execution of ... applies to internally sourced studies and studies out-sourced to Clinical Research Organizations (CROs) and the balance...are delivering per the scope of work + Ensure clinical project audit and inspection readiness through… more
- Regeneron Pharmaceuticals (Armonk, NY)
- The **Senior Manager Clinical Study Lead** (CSL) is expected to operate with high-degree of independence and is accountable for the global execution of assigned ... applies to internally sourced studies and studies out-sourced to Clinical Research Organizations (CROs) and the balance...are delivering per the scope of work + Ensure clinical project audit and inspection readiness through… more
- WMCHealth (Valhalla, NY)
- Project Manager Company: NorthEast Provider Solutions Inc. City/State: Valhalla, NY Category: Professional/Non- Clinical Department: Support Services- WMC ... (https://pm.healthcaresource.com/cs/wmc1/#/preApply/26882) Internal Applicant link Job Details: Job Summary: The Project Manager will be responsible for managing… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- This role resides in the Regeneron Genetic Medicines Clinical Development Unit and Experimental Sciences (RGM CDU & ES). The Manager , Strategic Planning & ... organization that is well-aligned and integrated with other functions, including RGM research , the Regeneron Genetic Center (RGC), and Global Development. **As a … more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- …and database research on clinical trials as needed + Collaborates with Clinical Project Managers and Clinical Trial Managers at the study level and ... with the Therapeutic Area Program Manager + Contributes to program team meetings, scientific advisory...experience. We are seeking Oncology training with translational and/or clinical research experience preferred. #MDJOBSCD, #MDJOBS, #GDTher… more
- Touro University (Hawthorne, NY)
- …clinical and analytical study related protocols and documents, as well as research / clinical data analysis. + Interface with investigational sites, clinical ... The candidate will report to the Vice President of Research . Incumbent will manage all aspects of ongoing ...timelines, budget and project protocols, progress, and project needs for clinical trials to product… more
- System One (Tarrytown, NY)
- …and implement strategies to mitigate them. Keywords: "Associate Manager ", " Research Program Manager ", "Program Management", " clinical trial", "program ... manager ", "T cell biology", "cell therapy", "vaccines", "antibodies", " project management", "drug development", "planning", "coordination", "operational guidance", "BS",… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- …a Senior Manager , HR Business Partner (HRBP) to support Regeneron's our Research & Pre Clinical Development, (R&pD) functions & business lines. This role ... Sr. HRBP and HR COE partners. **As a Senior Manager , HRBP a typical day may include:** + Partners...well as year-end compensation in Workday + Ad hoc project support (eg, career ladders, re-organization projects) **This role… more
- Grifols Shared Services North America, Inc (Stamford, CT)
- …**Medical Writer 1:** Typically requires 5 years of pharmaceutical experience in clinical research /regulatory medical writing. (If PhD, equivalency is 2 years ... **Medical Writer 2:** Typically requires 8 years of pharmaceutical experience in clinical research /regulatory medical writing. (If PhD in statistics, equivalency… more