- University of Pennsylvania (Philadelphia, PA)
- …of health and wellness programs and resources, and much more. Posted Job Title Clinical Research Regulatory Specialist B (Abramson Cancer Center) Job Profile ... Title Clinical Research Regulatory Specialist B Job Description Summary The...-CC to participate in the coordination of Phase I-V clinical trials . Reporting to the Regulatory… more
- 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
- J&J Family of Companies (Jacksonville, FL)
- …We are searching for the best talent to join our Vision team as a **Staff Clinical Trial Specialist ** located in **Jacksonville, FL** Fueled by innovation at ... to wellness. Learn more at https://www.jnj.com/medtech **Purpose:** The Staff Clinical Trials Specialist manages study...operating procedures and company policies are followed. The Staff Clinical Trial Specialist develops and… more
- Actalent (Durham, NC)
- … Job Description To maintain continuity and compliance across ongoing medical device trials , we are seeking a TMF Specialist to provide dedicated support ... CPMs, CRAs, and Data Managers to ensure documentation supports patient safety, regulatory compliance, and reliable trial outcomes. Work Environment This role… 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
- Sumitomo Pharma (St. Paul, MN)
- …International Council for Harmonization E6(R2). + Fundamental knowledge of the conduct of clinical trials is preferred. + Strong focus on teamwork, attention to ... our website https://www.us.sumitomo-pharma.com or follow us on LinkedIn. The Trial Master File (TMF) Specialist will be...ensure system validation is maintained. + Work closely with Clinical Operations and Regulatory Affairs to ensure… 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
- Georgetown Univerisity (Washington, DC)
- …Diseases Clinical Trials Unit will work with and assist the Clinical Research Coordinator, Regulatory Specialist , and Clinical Trial ... the Clinical Research Coordinator, Regulatory Specialist , and Clinical Trial Manager...7 years of experience working with clinical trials and supporting a clinical trial… 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
- Tufts Medicine (Boston, MA)
- …explanation of facts, policies and practices. **Job Overview** This position supports clinical investigators, research administrators, clinical trials , and ... or related field. 2. Three (3) years' experience in clinical trials research or research administration **Preferred...with research personnel to identify and quantify information impacting clinical trial finances. 6. Serves as one… more
- J&J Family of Companies (Irvine, CA)
- … Research Specialist will be responsible for supporting one or several clinical trials within the Clinical R&D Department while encouraging strong, ... R&D Department to support execution of company sponsored clinical trials , ensuring compliance with timelines and...feasibility, selection, set up, conduct and closure of a clinical trial within the allocated countries, in… more
- Edwards Lifesciences (Kansas City, KS)
- …clinical trial /study safety, in keeping with protocols, GCP (Good Clinical Practices) and regulatory requirements + Develop and deliver technical training ... make an impact:** + Field monitoring of studies and data collection for clinical trials , assess all data documentation, reports, records, transcripts, exam… more
- University of Utah (Salt Lake City, UT)
- …Quality Oversight** + Conduct routine internal audits and targeted reviews of clinical trial documentation including regulatory binders, subject binders ... research study teams, and clinical teams, the QA Specialist ensures regulatory compliance, operational efficiency, and consistently high standards… more
- Insight Global (Irvine, CA)
- …timelines. Collaborate with cross-functional teams ( Regulatory , Data Management, Clinical Operations) to ensure smooth trial execution. Maintain accurate ... role is critical in ensuring high-quality site management and operational excellence across clinical trials . Key responsibilities include but are not limited to:… more
- J&J Family of Companies (Danvers, MA)
- …testing, and site closeouts. As a subject matter expert on clinical trial protocol and technologies, the Field Research Specialist acts a liaison between ... clinical background in procedural areas. The Field Research Specialist is a dual-role position that combines field-based ...call, bedside case coverage for multiple clinical trials and clinical trial sites.… more
- Abbott (Abbott Park, IL)
- …114,000 colleagues serve people in more than 160 countries. **Job Title** **Senior Field Clinical Specialist ** **Working at Abbott** At Abbott, you can do work ... **The Opportunity** We currently have an opportunity available for a **Senior Field Clinical Specialist ** to join our **Vascular** division. **This is a fully… more