- Baylor Scott & White Health (Dallas, TX)
- **JOB SUMMARY** The Clinical Research Regulatory Specialist supports clinical research activities through the development of protocol-specific documents ... to research involving human subjects. This position also provides regulatory guidance and direction to internal clinical ... requirements are met, to include ensuring requirements for trial registration, results and reporting are completed in a… more
- Emory Healthcare/Emory University (Atlanta, GA)
- …+ The Regulatory Specialist III is an advanced level position supporting regulatory affairs in clinical trials research. + Employees in this job ... Establishes and maintains processes and monitors practices to ensure regulatory documentation involving clinical trials .... + Leadership and training: May supervise and train Regulatory Specialist I and II staff, lead… more
- University of Pennsylvania (Philadelphia, PA)
- …of unit research, including but not limited to Phase I-IV clinical trials . The Regulatory Affairs Specialist C will, independently prepare and ... documentation/ Trial Master files (TMF) as required. The Regulatory Affairs Specialist C is expected to...but not limited to Phase I-IV clinical trials . The Regulatory Affairs Specialist … more
- Stanford University (Stanford, CA)
- …107768 The Blood & Marrow Transplantation and Cellular Therapy (BMT-CT) Divisionis seeking a Clinical Trials Regulatory Specialist II position to support ... Regulatory Specialist (Hybrid Opportunity) **School of...a very active clinical trials faculty. The position will anticipate and generate reports… more
- Houston Methodist (Houston, TX)
- …event reports, safety reports, and notifies IRB of study closures. + Maintains the required regulatory files for all clinical trials to ensure regulatory ... and study specific protocols/plans and processes. The Regulatory Compliance Specialist position maintains documentation for clinical research studies, case… more
- Hackensack Meridian Health (Hackensack, NJ)
- …Minimum of 2 years experience in a Senior Clinical Data Coordinator or Senior Regulatory Specialist role, or at least 4 years related experience in the field ... and overseeing clinical operations of all assigned clinical trials and participates in assessing, planning,...general supervision of the principal investigator responsible for the clinical trial (s) to which is assigned. **Education,… more
- HonorHealth (AZ)
- …(CTMS), and familiarity with basic finance and accounting principles. The successful Clinical Trial Operations Specialist will support Research Program ... Research Administration, and the research staff. The tasks the Clinical Trial Operations Specialist must...closely with Principal Investigators, Clinical Program Leads, Regulatory , Finance, Clinical Trials Personnel,… more
- Terumo Neuro (Aliso Viejo, CA)
- **12870BR** **Title:** Sr Specialist , Clinical Trial Quality Assurance **Job Description:** Provide support to all aspects of the Clinical Quality ... Hiring Ordinance, and San Francisco Fair Chance Ordinance. **External-Facing Title:** Sr Specialist , Clinical Trial Quality Assurance **Posting Country:** US… more
- Houston Methodist (Houston, TX)
- …accurate data collection, documentation organization, and safety of study volunteers. Ensures accurate regulatory filing. + Assists Clinical Trial Manager in ... is responsible for supporting multiple projects under supervision of Clinical Trial Manager which may include ...from conceptual bench research, to prototyping and development, to clinical trials and FDA approval. The Research… more
- Organon & Co. (Plymouth Meeting, PA)
- **Job Description** **The** **Position** The Clinical Trial Manager (CTM), Translational Medicine and Early Development (TMED) is responsible for assisting in ... vendors. The CTM will also assist to manage the clinical study team and help to coordinate meetings and...defining, monitoring and reporting on all aspects of key trial performance indicators, including for example, country and site… more