- Vitalief (New Brunswick, NJ)
- …Join us and help clients adapt to evolving requirements in the research and clinical trial industry with cutting-edge solutions. Reasons to Work for Vitalief: + ... patient recruiting/pre-screening/consenting/retention; activation; regulatory compliance, data management. and other clinical trial activities for solid tumor, high… more
- Rockefeller University (New York, NY)
- …and new investigator audits, tracks deviations for early intervention, and supports clinical trial registration in Good Clinical Practice (GCP) ... For more information,please see the hospital website at: http://www.rucares.org/ Overview The Clinical Research Specialist serves as a regulatory expert and… more
- Merck (North Wales, PA)
- …Data Tabulation Model (SDTM) + A broad comprehensive knowledge of the clinical trial process including data management (data collection, processing, storage, ... regulations + Ensuring the definitions are maintained and aligned across the clinical lifecycle (eg, data collection, analysis & report, and submission) deliverables… more
- System One (Plainsboro, NJ)
- …quality, performance, regulatory compliance, and patient safety related to managing assigned clinical trial sites and document handling. + Attends and ... the main goal. They are seeking a Senior Retention Specialist to support patients enrolled in the clinical... trials. + A minimum of 5 years of clinical trial experience within a pharmaceutical, biotechnology,… more
- Medtronic (New Brunswick, NJ)
- …RESPONSIBILITIES:** The following responsibilities are to be performed as appropriate in clinical trial case support and/or case support following commercial ... EKG, blood pressure, wave forms, and ancillary procedural solutions + Knowledge of Clinical trial protocols, and CoreValve and other Medtronic TAVR product IFUs… more
- ThermoFisher Scientific (Bridgewater, NJ)
- … clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy ... FSO, FSP, Government, etc.). Acts as a site processes specialist , ensuring that the trial is conducted...study systems are updated per agreed study conventions (eg Clinical Trial Management System, CTMS). Performs QC… more
- Abbott (New York, NY)
- …heart arrhythmias, or irregular heartbeats. **WHAT YOU'LL DO:** The Regional Leadless Specialist provides technical, clinical , educational and sales support to ... ensure adoption and growth of Abbott leadless technology. The Regional Leadless Specialist works closely with internal and external customers to drive therapy… more
- Merck (Trenton, NJ)
- …exposure-response, quantitative system pharmacology, and other model-based analyses. + Perform clinical trial simulations to inform dose selection and go/no-go ... -** **Immune/Oncology** **(QP2-IO)** team in the role of Senior Specialist . QP2-IO team is part of the Global ...Specialist . QP2-IO team is part of the Global Clinical Development organization and has oversight over drug development… more
- Hackensack Meridian Health (Neptune, NJ)
- …works under the general supervision of the principal investigator responsible for the clinical trial (s) to which is assigned. **Responsibilities** + Acts as ... on each protocol and each patient participating in a clinical trial protocol in the clinical...+ Minimum of 2 years experience in a Senior Clinical Data Coordinator or Senior Regulatory Specialist … more
- Medtronic (New York, NY)
- …stakeholders to determine appropriate clinical evaluation strategy; may provide input to clinical trial design + Identify potential evidence gaps or risks to ... and communicate risks as needed + Stay current on clinical evidence landscape and provide guidance to teams on...sufficient data + Develop and maintain in-depth knowledge of clinical evaluation best practices and regulatory agencies' guidelines on… more
- Actalent (New York, NY)
- …IRB/IEC and other applicable regulations/guidelines. Demonstrated basic understanding of the clinical trial process Education: Level of education preferred (if ... burn with the support of more senior specialists Skills: Contract, clinical research, contracts, negotiation, Regulatory Top Skills Details: Contract, clinical … more
- Novo Nordisk (Princeton, NJ)
- …with teams in departments throughout the organization, including Medical Affairs, HEOR, Clinical Trial Management, Market Development & HCP Engagement, as well ... the head of Rapid Cycle Analytics (RCA) and functions as an analytics specialist in the Clinical Data Science & Evidence (CDSE) department. Collaborates closely… more
- Bristol Myers Squibb (Trenton, NJ)
- …achieve annual goals + Leverages digital capabilities to enhance medical engagement ** Clinical Trial ** **engagement** + Provides recommendations and insights to ... equity in access to clinical trials. + Leads major evidence read-outs with clinical trial investigators eg, Ph 3 top-line data. + Support Interventional and… more
- Bristol Myers Squibb (Princeton, NJ)
- …and ethical standards + Ensures active participation of FM in providing input on clinical trial site selection and feasibility based on their knowledge of ... investigators in their geography + Ensures FM team's execution of clinical trial support activities (as per established study scope documents) + Ensures that FM… more
- University of Pennsylvania (Philadelphia, PA)
- …Budget Specialist , Billing Compliance staff, and Finance office to develop clinical trial budgets. Communicating any specialized study budget needs to the ... is a world leader in developing and conducting innovative clinical trials for the prevention, diagnosis, and treatment of...budget specialist , including any changes necessitated by a protocol modification… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …and manage campaign performance throughout enrollment. **ACCOUNTABILITIES:** + Support trial -specific patient recruitment and retention efforts partnering with a ... + Lead study-specific recruitment programs working closely with the clinical study teams, vendors, and CRO as applicable. +...vendors, and CRO as applicable. + Work with PR&R specialist to conduct early operational planning and research to… more
- Pfizer (New York, NY)
- …ICH, and National regulations). **ROLE RESPONSIBILITIES** + Assesses compliance of GCP clinical trial sites and processes against ICH GCP and applicable ... other areas of the business + Acts as a specialist in specific therapeutic area or specialty (eg gene...gene therapy) and/or audit topic (eg data management, remote trial methodology etc.) + Candidate demonstrates a breadth of… more