- ThermoFisher Scientific (Wilmington, NC)
- …clinical deliverable (usually clean data from evaluable patients as specified in the study protocol) within the time period specified in the contract with the ... moderate to high complexity and may assume regional lead or Clinical Study Manager responsibilities. **Essential Functions:** + Leads all clinical operational and… more
- ICON Clinical Research (New York, NY)
- …projects progress with respect to milestones, budgets and timelines. + Manage bioanalytical studies to ensure that bioanalysis is well coordinated with in life ... study phases, and that samples are appropriately tracked throughout...including tracking of revenue and resources associated with assigned studies . + Identify changes to scope of work as… more
- University of Pennsylvania (Philadelphia, PA)
- …collection, entry, and tracking; reviews medical or research data for study eligibility; and helps prepare documentation for compliance and reporting. Contributes ... to reviews to the IRB, literature reviews, reports, and other study -related materials while coordinating routine lab or departmental operations. Job Description Job… more
- Ascendis Pharma (Palo Alto, CA)
- …will be expected to provide timely and strategic programming support to clinical study teams in alignment with project goals. This role combines hands-on programming ... responsibilities with leadership in study execution and tool development. The successful candidate will...specification templates of SDTM and ADaM used across clinical studies . This position requires expertise in CDISC standards (SDTM,… more
- Actalent (Palo Alto, CA)
- …research participants, sponsors, and regulatory agencies. You will coordinate clinical studies from startup through close-out, ensuring compliance with all protocols ... in the field of clinical research. Responsibilities + Determine eligibility of study participants and gather consent according to protocol. + Assist in developing… more
- University of Pennsylvania (Philadelphia, PA)
- …and lab studies , including IRB, and NIH regulatory documentation. Follow study protocols and SOPs to recruit potential research participants, study ... Job Description Job Responsibilities + Coordinate day-to-day management of clinical research studies + Maintain study regulatory documents + Follow research… more
- ThermoFisher Scientific (Carlsbad, CA)
- …clinical deliverable (usually clean data from evaluable patients as specified in the study protocol) within the time period specified in the contract with the ... high complexity and may assume regional lead or Clinical Study Manager responsibilities. What You'll Do: + Manage all...Manage all clinical operational and quality aspects of allocated studies , of moderate to high complexity, in compliance with… more
- J&J Family of Companies (Santa Clara, CA)
- …The Sr. Field Clinical Engineer will play a critical role in clinical studies including device training, case support, and ensuring timely data collection for ... to ensure the safe and effective use of medical devices. + Present clinical study training materials based on investigational plans to support the safe and effective… more
- University of Miami (Boca Raton, FL)
- …monitors subjects' responses. + Conducts initiation visits and registers patients in clinical studies . + Performs study data collection and entry using charts, ... Research Nurse 1 ensures the integrity and quality of clinical research studies are maintained and conducted in accordance with practice guidelines, federal and… more
- Stanford University (Stanford, CA)
- …Programis seeking an Assistant Clinical Research Coordinator (ACRC) to support the clinical studies . This position is expected to work onsite, engage in all facets ... of research, including study recruitment and enrollment, grant writing, abstract/manuscript writing, designing...accuracy. + Extract data from source documents for research studies as directed. Collect data and complete case report… more