- Merck & Co. (Rahway, NJ)
- Job DescriptionPosition Description: Associate Clinical Research Manager (aCRM) - Oncology With support of other Clinical Research Manager 's (CRMs) ... requirements internally and externally.The aCRM could be responsible for a particular study for a country or a cluster.Responsibilities include, but are not limited… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionUnder the direction of the applicable management, the Lead Clinical Data Manager (LCDM) is responsible for executing end to end data management ... are not limited to: All responsibilities of a Senior Clinical Data Manager (SCDM) and a ...to identify and incorporate global operational issues into the study design.Execute and trigger communications and escalations at the… more
- Merck & Co. (Rahway, NJ)
- …of Clinical Trial Research Agreements (CTRA).Oversees and tracks clinical research-related payments. Payment reconciliation at study closeout. Oversees ... quality standards and adverse event reporting requirements internally and externally.Our Clinical Research and Pharmacovigilance team push the boundaries of global… more
- Tris Pharma (Monmouth Junction, NJ)
- … clinical study work May also function as a Clinical Trial Manager (CTM), as neededRequirementsSpecial knowledge or skills needed and/or licenses ... cross functional collaboration to develop program strategy and the implementation of clinical study processes and procedures ensuring timely execution of quality… more
- Merck & Co. (North Wales, PA)
- …least 2 years of experience in publication managementUnderstanding of the clinical development process andclinical study data for assigned ... Job DescriptionOverview:The Associate Director Publication (Pub) Manager is the central source of information regarding publication activities and is responsible for… more
- Merck & Co. (North Wales, PA)
- …regions simultaneously.Reviews and provides final approval Worldwide Marketing Applications, Clinical Study Reports, Protocols, Investigators' Brochures before ... single point-of-contact for products within Global Regulatory Affairs and Clinical Safety (GRACS) and external to GRACS.Develops worldwide product regulatory… 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
- Stryker (Cary, IL)
- …patients annually. More information is available at www.stryker.com We are currently seeking a ** Clinical Study Manager ** , to join our **Medical** Division. ... regulations and expectations. **What you will do** As a ** Clinical Study Manager ** , you... clinical regulatory documentation preparation and submissions for clinical studies (eg, IDE submissions, IRB/EC submissions).… more
- Actalent (Bethesda, MD)
- … operations, or clinical trial monitoring/management experience, eg, clinical study design, conduct, management, reporting, and/or product development ... Position Summary: Seeking a Clinical Project Manager to join a...activities associated with the conduct and successful performance of clinical trials/ studies with demonstrated expertise and ability… 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 ... - $52.53Qualifications Required: * Bachelor's degree or 1-3 years of previous study coordination or clinical research coordination experience * Strong verbal… more
- Stanford University (Stanford, CA)
- Cancer Clinical Research Project Manager - Data Quality & Study Start- Up ( Hybrid ) **School of Medicine, Stanford, California, United States** **New** ... Requisition # 103005 Cancer Clinical Research Project Manager - Gyn-Onc ( Hybrid ) The Stanford Cancer...CCRPM will provide oversight for data management integrity and study start-up process across a cancer clinical … more
- Stanford University (Stanford, CA)
- Cancer Clinical Research Project Manager - EDD Data quality and study Start-Up ( Hybrid ) **School of Medicine, Stanford, California, United States** ... Requisition # 102577 Cancer Clinical Research Project Manager - Early Drug Development ( Hybrid ) The...conduct industry sponsored trials, cooperative group trials, investigator initiated clinical research studies , from start up to… more
- Boehringer Ingelheim (Ridgefield, CT)
- …terminology coding for all program types including but not limited to clinical trials, non-interventional studies (NIS), Investigator Initiated Studies ... Ingelheim's high regard for our employees. This is a hybrid position which requires 2 days a week onsite...event information reported and collected. + Participate in the study development and startup activities for both clinical… more
- Actalent (Bethesda, MD)
- …experience Hybrid Schedule 3 days work from home 2 days in office Hybrid Clinical Project Manager Plan and manage day-to-day operational aspects of ... and propose solutions to improve efficiency and quality of deliverables Represent clinical -trial related operations at study team meetings, participate 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)
- …. 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)
- The Clinical Studies Coordinator collaborates with the research team and principal investigator in managing research protocols, assuring protocol compliance, ... Excel, and others as designated. * Consults with PI and the Research Nurse Manager regarding ongoing study assignments. Collaborates with other members of the… more
- MD Anderson Cancer Center (Houston, TX)
- Coordinator, Clinical Studies MISSION STATEMENT The mission of The University of Texas M. D. Anderson Cancer Center is to eliminate cancer in Texas, the nation, ... assignments as needed/requested. EDUCATION Ensures the conduct of assigned studies is in accordance with Good Clinical ...protocol related data and provide protocol guidance to the Clinical Study and Research Data Coordinators. SAMPLE… more
- University of Pennsylvania (Philadelphia, PA)
- …under general supervision. Assist CTT program manager with initiating study procedures for new industry-sponsored and investigator-initiated clinical trials. ... website (https://coronavirus.upenn.edu/) for the latest information. Posted Job Title Clinical Research Coordinator B/C ( Hybrid Eligible)(Abramson Cancer Center)… more
