- HCA Healthcare (Overland Park, KS)
- …for emotional, physical and financial wellbeing + 401(k) Plan with a 100% match on 3 % to 9% of pay (based on years of service) + Employee Stock Purchase Plan ... (https://careers.hcahealthcare.com/pages/employee-benefits-and-rewards) The **Clinical Research Coordinator (CRC)** assists the principal investigator (PI) and sub investigators with all aspects of… more
- University of Pennsylvania (Philadelphia, PA)
- …research protocols, as well as assist in the conduct of investigator -initiated research and division-specific research projects and operations. This position's ... in study team meetings, disease site group meetings, and ongoing protocol training/ compliance meetings. Supports in the monitoring of external sites and assists in… more
- US Tech Solutions (North Chicago, IL)
- …Communication Skills; providing updates across functions; written and verbally 3 . **Contractual or Paralegal** experience highly preferred **Purpose:** The Contract ... including **Clinical Study Agreements, Confidential Disclosure Agreements, Master Agreements, Investigator Initiated Agreements, Service Agreements** ect In partnership with… more
- Dayton Children's Hospital (Dayton, OH)
- …of the Clinical Research Supervisor/Operations Manager and a Principal Investigator (PI) while adhering to International Conference on Harmonization (ICH),Good ... participating in research at DCH, and assistance in monitoring research compliance with all applicable regulations, guidelines and policies. Department Specific Job… more
- Stanford University (Stanford, CA)
- …**School of Medicine, Stanford, California, United States** **New** Research Post Date 3 days ago Requisition # 107255 The Stanford Stroke Center is seeking ... ensuring that all activities are conducted efficiently, accurately, and in compliance with regulatory requirements. This position offers the opportunity to… more
- US Tech Solutions (Cambridge, MA)
- …- GI is needed** and in **GI- pancreatic cancer exp. is preferred** + ** 3 -5+ years** of **oncology MSL experience is required.** + **A doctorate degree is ... adheres to internal standard processes and complies with regulatory and compliance requirements along with sustaining expertise in disease state management, emerging… more
- Bozeman Health (Bozeman, MT)
- …(NCI), and other regulatory agencies. Responsibilities include ensuring protocol compliance , recruiting and caring for study participants, documenting study ... Bozeman Health policy, and other registry requirements. + Ensure compliance with research protocols, regulatory requirements, and institutional policies while… more
- Colorado State University (Fort Collins, CO)
- …on the island of Guam, a self-governing territory of the United States located 3 ,300 miles west of Hawaii and 1,500 miles east of the Philippines. Guam averages ... ( CATR ), CEMML Cultural Resources Project Director, and CEMML Principal Investigator . This is a full-time position primarily based in Guam, with potential… more
- Sanofi Group (Cambridge, MA)
- …development documents including clinical development plans, SAPs, study protocols, investigator brochures, data monitoring plans, study reports, integrated summary ... of risk mitigation or other corrective actions as necessary + Regulatory compliance + Monitoring of risk mitigation tool effectiveness and adjustment of strategy,… more
- US Tech Solutions (North Chicago, IL)
- …**Clinical Study Agreements, Confidential Disclosure Agreements, Master Agreements, Investigator Initiated Agreements, Service Agreements** ect In partnership with ... Communication Skills; providing updates across functions; written and verbally 3 . **Contractual or Paralegal** experience highly preferred **Responsibilities:** *… more