- Merck & Co. (Rahway, NJ)
- …requirements internally and externally.The CRM could be responsible for a particular study for several countries in a cluster. Responsibilities include, but are not ... Contact (POC) for assigned protocols and link between Country Operations and clinical trial team (CTT).Responsible for project management of the assigned studies… more
- Merck & Co. (Rahway, NJ)
- … Clinical Research, the individual is responsible to-manage/oversee a team of CTCs( Clinical Trial Coordinator).As line manager the role is critical to ... role will work across the different country operations roles (eg CRM( Clinical Research Manager ), CRA( Clinical Research Associate)- Manager… more
- Merck & Co. (North Wales, PA)
- …with the Medical Writer on clinical /scientific and regulatory documents.Partners with Study Manager on study deliverables.Participates in the set up ... Job DescriptionThis position drives scientific planning, strategy and execution of Phase 1-4 clinical studies .-Under the direction of the Program Lead, you will… more
- Merck & Co. (Rahway, NJ)
- …primary site contact and site manager -throughout all phases of a clinical research study , taking responsibility of allocated sites.Develops strong site ... CRA/CRA and/or CRA Manager , acts as...continuity of site relationships through all-phases of the trial.Performs clinical study site management/monitoring activities in compliance… more
- Merck & Co. (Rahway, NJ)
- …for a wide range of stakeholders including the Global Project Manager , Alliance Manager , Global Trial Manager , Clinical Sub Team, Clinical Trial ... improve lives. -Position Description: Under the guidance of the Oncology Clinical Development Finance Associate Director, the Finance Senior Specialist will:Provide… more
- Merck & Co. (Rahway, NJ)
- …and disseminates a portfolio of prioritized real-world evidence/outcomes research studies and outcomes research activities linked to value and implementation ... goals.- Manages study and activity budgets and records milestone timing. -Provides...Epidemiology, Pharmaceutical Administration, Public Health, Health Policy, Medicine, or Clinical Pharmacy)- 7+ years relevant experience following advanced or… more
- Stanford University (Stanford, CA)
- Network Clinical Research Manager ( Hybrid ), Cancer Center South and East Bay **School of Medicine, Stanford, California, United States** Research Post Date ... Clinical Research Manager - Cancer Center South and East Bay ( Hybrid Work Arrangement)** The Stanford Cancer Institute's Clinical Trials Office (SCI-CTO)… more
- Stryker (Mahwah, NJ)
- …precision. **What you will do** As the ** Clinical Study Manager (CSM),** you will manage ongoing Investigator-Initiated Studies and/or Stryker Initiated ... Study Manager ** to support Joint Replacement Clinical Trials. This role will be based ** hybrid...research strategy. + Develop and maintain overall dashboard of clinical and non- clinical studies , including… more
- UCLA Health (Los Angeles, CA)
- … Clinical Data Manager will be responsible for data management of clinical research studies . You will collect and transcribe research patient data and ... - $52.53 Qualifications Required: + Bachelor's degree or 1-3 years of previous study coordination or clinical research coordination experience + Strong verbal… more
- ManpowerGroup (Bethesda, MD)
- …will align successfully in the organization. **Job Title: Clinical Project Manager ** **Location: Bethesda, MD ( Hybrid with 2 days onsite)** **Pay Range: ... Our client is seeking a Clinical Project Manager to join their...equivalent experience. + This person will support 1 trial study at max 2-3 trials at a time. +… more
- Actalent (Philadelphia, PA)
- Description: Hybrid Clinical Project Manager (1-2 days on site in Center City Office) - Organization and key management activities related to clinical ... management procedures and work practices for the organization. Top Skills Details: Clinical , Project Manager , Oncology, Timeline Management Additional Skills &… more
- ConvaTec (Lexington, MA)
- …regulations. **Key responsibilities and authority:** + Proactively manage assigned clinical studies . + Support clinical study delivery across Clinical ... Join us on our journey to #ForeverCaring as a Clinical Study Management Specialist, and you'll do...Role:** Provide operational expertise to ensure effective delivery of clinical studies across Convatec's Business Units. Reporting… more
- Actalent (Basking Ridge, NJ)
- …developed in house ! This company has great culture and is rapidly growing! Summary: The Clinical Study Associate Manager role supports the Clinical ... versus oversight of CROs deliverables will vary accordingly. The Clinical Study Associate Manager works... sites may be required to assist with monitoring clinical studies . Qualifications: + 5+ years of… more
- Taiho Oncology (Pleasanton, CA)
- …+ Coordinates cross functional study team meetings and supports study manager with meeting minutes for assigned studies . + Updates internal study ... it most. This is an exciting opportunity to support clinical studies and experience multiple facets of...site-related documentation, and inspection readiness. + Collaborates closely with study manager to align expectations and … more
- Regeneron Pharmaceuticals (Armonk, NY)
- …for this role. The position can be based in Armonk, NY or Basking Ridge, NJ._ A Clinical Study Associate Manager (CSAM) role supports the Clinical ... sites may be required to assist with monitoring clinical studies . **A typical day as CSAM...like:** + Lead/oversee the planning and management of a clinical study in an assigned region(s) in… more
- International Rescue Committee (New York, NY)
- Requisition ID: req45075 Job Title: Clinical Program Manager , Home Study and Post-Release Services Sector: Social Work Employment Category: Fixed Term ... 82,000.00 Annually Location: New York, NY HQ USA Work Arrangement: Hybrid Job Description SCOPE OF WORK: The IRC's Home... Job Description SCOPE OF WORK: The IRC's Home Study and Post-Release Services (HSPRS) for unaccompanied children in… more
- MD Anderson Cancer Center (Houston, TX)
- Senior Coordinator, Clinical Studies - Thoracic-Head & Neck Medical Oncology JOB SPECIFIC COMPETENCIES Protocol Management -Independently performs ... improving activation times for new protocols.. -Develops, recommends and implements necessary clinical study revisions for PI's approval. -Oversees the overall… more
- CSL Behring (King Of Prussia, PA)
- …biotherapies used to treat serious and often rare conditions. Could you be our next Senior Clinical Lab Study Manager ? This position is located in our King ... Germany, Maidenhead UK or Amsterdam office. It is a Hybrid role. You will have multiple direct reports. You...laboratory teams and will work with the program directors, clinical teams and R&D teams offering scientific and strategic… more
- MD Anderson Cancer Center (Houston, TX)
- …. Under supervision of the protocol primary investigator (PI), the research nurse manager and/or clinical studies supervisor, assumes responsibility for the ... **JOB SPECIFIC COMPETENCIES** **Coordination of Study initiation and Operations of Clinical ...participating institutions and coordinates all data pertaining to such studies . . Sets up monitoring visits - Schedules the… more
- MD Anderson Cancer Center (Houston, TX)
- **Summary** The Clinical Studies Coordinator collaborates with the research team and principal investigator in managing research protocols, assuring protocol ... Excel, and others as designated. . Consults with PI and the Research Nurse Manager regarding ongoing study assignments. Collaborates with other members of the… more
