Clinical Trials Regulatory Coordinator — Drive Study Compliance
UNLV
UNLV's Clinical Trials Regulatory Coordinator in the Research Department supports the regulatory lifecycle of clinical studies, ensuring regulatory documents and submissions are complete, accurate, and compliant. This role serves as the primary liaison between investigators, IRB, study sponsors, and regulatory agencies, guiding trials from activation through close-out while upholding GCP, FDA regulations, and institutional standards. #J-18808-Ljbffr UNLV
- Profound Research seeks a Clinical Research Coordinator II to manage assigned studies on-site, from start-up through closeout, coordinating patient visits... ...interactions while ensuring audit-ready documentation and regulatory compliance. You will work directly with investigators,...Regulatory
- IQVIA is seeking a Global Study Manager to lead end-to-end... ...management for global oncology trials. You will own site... ...functional teams to ensure compliance with ICH-GCP and regulatory standards. Responsibilities... ...monitoring timelines, and driving risk mitigation. #J-18808...Regulatory
- ...development, transactions, operations, and regulatory compliance. We are honored to have received the... ...and RESPONSIBILITIES The Transaction Coordinator primarily supports RTG’s portfolio... ...Finance, Real Estate, Healthcare, Paralegal Studies or a related field is required....RegulatoryFull timeContract workWork experience placementWork at office
$60.01k - $88.01k
...position is in the Cancer Clinical Trials Office (CCTO), supporting multiple... ...groups and PI initiated studies), and respond to IRB... ...study documents to support regulatory compliance, and troubleshoots processes... ...Israel Lahey Health, we are driving the change in health care that...RegulatoryWork experience placementWork at officeLocal areaImmediate start- Clinical Research Associate - Full-Service Syneos... ...) ensuring regulatory, ICH‑GCP and/or Good... ...GPP) and protocol compliance. Use judgment and... ...as necessary, and drive query resolution to... ...conduct of clinical study data review and... ...reconcile it with the Trial Master File (TMF),...RegulatoryInterim roleLocal areaImmediate startRemote workFlexible hours
$164k - $214k
The Senior Clinical Trial Manager will lead, manage... ...trials from study start-up to close... ...terms of quality, compliance, budget, and timing... ...office. Lead and coordinate a cross-... ...for resolution. Drives the selection of... ...of international regulatory and ICH Good Clinical...RegulatoryWork at officeLocal areaRelocation package- ...sites meeting the clinical research needs of global... ...in accordance with regulatory compliance. Conducting studies since 1984, M3 Wake... ...potential clinical trial participants across... ...Clinical Research Coordinator at Wake Research ,... ...the chance to drive change with M3 USA....RegulatoryFlexible hours
- Experienced Clinical Research Associate - Sponsor... ...) ensuring regulatory, ICH‑GCP and/or Good... ...GPP) and protocol compliance. Uses judgment and... ...staff as necessary, driving query resolution... ...conduct of the clinical study data review and... ...the ISF with the Trial Master File (TMF)....RegulatoryContract workInterim roleLocal areaImmediate startRemote workFlexible hours
- ...Franklin, IN is seeking an experienced MDS Coordinator RN to lead the Resident Assessment Instrument process, ensure regulatory compliance, and drive interdisciplinary care planning across... ...Village campus. The role emphasizes clinical judgment, collaboration with nursing...Regulatory
$24.87 per hour
...American Red Cross is seeking a Team Lead/Charge to support mobile blood drive operations in Montgomery County, PA. You will coach the team, perform phlebotomy as needed, and ensure compliance with regulatory requirements while delivering exceptional donor service. We offer...RegulatoryHourly pay$259k - $314k
...Senior Director, Clinical Operations... ...global clinical trials, especially... ...actionable plan, and drive delivery... ...across multiple studies and... ...Investigators and study coordinators Partner closely... ..., Safety, Regulatory, Biometrics, Clinical... ...training for compliance with GxP...RegulatoryFlexible hoursShift work- ...and workers compensation programs to ensure compliance with OSHA, Cal/OSHA and all applicable local, state and federal regulatory requirements. Main Duties and... ...with government agencies. Responsible for coordinating the medical management of Workers Compensation...RegulatoryLocal area
$262.06k - $306.73k
...Phase 3 outcomes trial is evaluating... ...Senior Director, Clinical Operations provides... ...programs from study start-up through... ...while maintaining compliance with global regulatory requirements.... ...Operations will drive operational strategy... ...study teams. Coordinate and oversee Investigational...RegulatoryMinimum wageFull timeLocal areaFlexible hours- ...per policy, inventory. • Capable to understand contracting, applications, accreditation standards, regulatory standards • Capable to understand and implement compliance procedures under the pharmacist in charge’s direction • Organized in workflow • Able to meet...RegulatoryWork at officeFlexible hoursWeekend work
$59.3k - $90.3k
...Insurance Coordinator Explores, recommends, and coordinates insurance and... ...philosophy. Adheres to the FMCNA Compliance Program, including following all regulatory and company policy requirements.... ...with dialysis patients at the clinic(s) in the assigned region to educate...RegulatoryWork experience placementWork at officeLocal area- ...centers in Philadelphia, seeks an OCR Clinical Trial Research Monitor II to ensure protocol compliance at clinical research sites and oversee investigator-initiated studies. The role emphasizes oncology research experience and regulatory knowledge. The candidate must hold...Regulatory
$270k - $280k
...BioAge Labs is a clinical-stage biotechnology... ...experience leading trials in cardiovascular,... ...responsible for driving clinical operational... ...trial quality,GCP compliance and within budget.... ...activities from study start up through close... ...and review of regulatory filings as needed....RegulatoryWork at officeRemote workFlexible hours- ...Ruhlin Company seeks to hire an Onboarding Coordinator . The opening is based out of Ruhlin's... ...onboarding practices to strengthen compliance, efficiency, and the new hire experience... ..., and communicate project-specific and regulatory training requirements. Administer and facilitate...RegulatoryWork at office
- Elevate Clinical Research is seeking a Clinical Research Coordinator to coordinate and oversee the daily operations of clinical trials in healthcare settings. You will manage patient... ...visits while ensuring regulatory compliance and study integrity. The role requires...Regulatory
- ...role performs inspections, maintains documentation, monitors compliance with company and customer standards, and supports audit activities... .... Knowledge of HACCP, GMPs, sanitation procedures, and basic regulatory requirements preferred. Ability to perform inspections,...RegulatoryWork at office
- ...in maintaining educational quality and ensuring compliance with ACGME accreditation standards and regulatory requirements. Serve as a liaison between Program... ...Provide administrative support including office coordination, word processing, and file maintenance for Residents...RegulatoryTraineeshipInternshipWork at office
$158k - $185k
...is our people who drive this mission to... ...through Summit’s clinical studies in the field of oncology... ...approved by any regulatory authority other... ...Senior Clinical Trial Manager (Sr. CTM)... ...clinical trials coordinates, while leading... ...Practices. Ensure compliance of clinical trials...RegulatoryContract workFor contractorsFor subcontractorWork at office- ...delivering high-quality Phase I-IV clinical trial execution to help sponsors... ...Job Description: The Regulatory Affairs Assistant supports... ..., the Regulatory Coordinator is guided by Good Clinical Practices... ...Investigator Site File for all awarded studies. Collect signatures on...RegulatoryWork at office
- Excelya Group seeks a Senior CRA/Site Monitor II to oversee clinical trial monitoring for oncology studies, ensuring data integrity and regulatory compliance. Travel to sites will be required, with some remote monitoring where allowed by local regulations. The ideal candidate...RegulatoryRemote jobLocal area
- Artivion, Inc. is seeking a Clinical eTMF Specialist to manage the electronic Trial Master File across... ...trials, ensuring GCP/ICH compliance and inspection... ...functional teams, CROs, and study sites to maintain accurate... ..., and supporting regulatory inspections, with travel...RegulatoryRemote job
- ...of Hope in Duarte, California, seeks a full-time Clinical Study Coordinator to support oncology trials on-site. You will coordinate participant... ...consent, trial coordination, data management, and regulatory compliance in a fast-paced environment. The successful candidate...RegulatoryFull time
- Stanford University’s Clinical Research Hub (CRH) seeks a mission-driven Clinical Trials Regulatory Specialist 2 to ensure regulatory compliance and effective collaboration across clinical operations... .... The role involves interface with study teams, IRBs, FDA, and other...RegulatoryRemote workFlexible hours
- Sprouts Farmers Market seeks a detail-oriented Pricing Coordinator to ensure pricing accuracy and compliance across the store network. You will partner with... ...and signage, while upholding company policies and regulatory standards. Responsibilities include price checks, updating...Regulatory
- ...a detail-oriented Research Coordinator to assist in coordinating patient... ...and data collection for clinical studies in a supportive academic setting. You will handle regulatory documentation, IRB submissions... ..., while ensuring protocol compliance and patient safety under supervision...Regulatory
- Medical University of South Carolina seeks a Clinical Research Assistant to support the regulatory team in maintaining compliance for program studies. You will manage regulatory files, keep documents updated and ready for site monitors, and help prepare audits. The role...RegulatoryWork at office
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