Clinical Research Coordinator - Trials, Data & Compliance
Cenexelresearch
CenExel Clinical Research is a leading nationwide clinical research site and patient network. We coordinate clinical trials with strict adherence to ICH, GCP, and sponsor guidelines, ensuring data integrity and patient safety across multiple centers. As a Clinical Research Coordinator, you will support trial initiation, patient involvement, data collection, and regulatory documentation while collaborating with investigators, vendors, and sponsors to maintain high-quality study conduct. #J-18808-Ljbffr Cenexelresearch
- ...Cancer Center in Seattle is seeking a Clinical Research Coordinator to manage investigator-initiated... ...industry-sponsored human subjects trials with compliance and independence under supervision.... ...You will oversee daily operations, data tools, and patient enrollment to support...DataRemote job
- Accel Research Sites is seeking a Clinical Research Coordinator to join the Operations team at Coastal Carolina Research Center... ...will ensure study execution in compliance with GCP, ICH, HIPAA, FDA... ...screening, consent, follow-up visits, data entry in EDC, vitals/ECGs, basic...Data
$164k - $214k
The Senior Clinical Trial Manager will lead, manage and co... ...in terms of quality, compliance, budget, and timing.... ...MA office. Lead and coordinate a cross-functional study... ...and CTMS systems and data maintenance. Tracks... ...and clinical research best practices. Ensures...DataWork at officeLocal areaRelocation package$158k - $185k
...lives through Summit’s clinical studies in the field... ...Role The Senior Clinical Trial Manager (Sr. CTM) is a... ...clinical trials coordinates, while leading and driving... ...quality study execution, data monitoring strategies... ...Practices. Ensure compliance of clinical trials with...DataContract workFor contractorsFor subcontractorWork at office$30.2 - $38.7 per hour
Cardinal Health is seeking a Clinical Research professional to coordinate clinical development planning, protocols, and trials across Phases 1-4. This position emphasizes independent... .... You will contribute to regulatory compliance and ongoing clinical research initiatives...SuggestedHourly pay- ...Presbyterian in Orange County, CA, seeks a Clinical Research Coordinator I (CRC-I) to support FDA-regulated... ...You will coordinate visits, consent, data entry, and sample handling, working with... ...ability to manage multiple concurrent trials in a fast-paced environment. #J-18808...Data
$36.31 - $58.41 per hour
...Monday-Friday #141770 Assistant Clinical Research Coordinator Filing Deadline: Wed 10/14/... ...assist operations, ensure compliance with state and federal... ...medical and clinical research data, and directly communicate... ...concerning the ongoing clinical trials, assist PIs with proposals,...DataHourly payContract workLocal areaMonday to Friday- Velocity Clinical Research is seeking a Clinical Research Coordinator I to conduct and manage clinical trials per protocol, GCP, and Velocity SOPs. You will coordinate startup activities... ..., regulatory documentation, and data handling while ensuring patient safety and...DataLocal area
- ...Center of Florida, Inc. in Miami Beach seeks a Clinical Research Coordinator to screen participants, document progress, and support protocol adherence across trials. You will interact with patients and families, coordinate data entry, and assist with regulatory...Data
$29.05 - $44.28 per hour
## Clinical Research Coordinator IIApply: Hybrid (Part -time in Office): Clinical Support... ...path within Clinical Trials. It is a development career... ...subjects, ensuring protocol compliance and close monitoring while... ...analysis of situations or data requires a review of a variety...DataFull timePart timeWork experience placementWork at office$56.2k - $81.5k
...motivated and detail-oriented Clinical Research Coordinator (CRC) to support a diverse... ..., administrative, and data-related aspects of research... ...all studies are conducted in compliance with institutional policies... ...documentation (e.g., IRB, Clinical Trials Office)* Assist with grant...DataFull timeWork experience placementWork at officeRemote work- ...an experienced Registered Nurse to manage clinical research trials with physicians, ensuring patient safety and protocol compliance. The role emphasizes evidence-based care and... ...collaboration with multidisciplinary teams, accurate data recording, and strict adherence to GCP...DataRemote job
- ...in Philadelphia seeks a Senior Clinical Research Coordinator to oversee day-to-day trial activities in line with GCP standards... ..., enrollment, consenting, data handling, and regulatory tasks.... ...protocol adherence and regulatory compliance, staff training, IRB submissions...Data
- ...Children’s Hospital is seeking a clinical research professional to independently... ...implementation, and prepare data collection and analytical reports... ...team. The role involves coordinating trial activities, ensuring regulatory compliance, and supporting SOP updates and...Data
$34 per hour
...Assistant Clinical Research Coordinator 1503779 ~ Hourly pay: $34/hr ~ Worksite: Leading university... ...with participant recruitment, data collection, regulatory documentation, and study operations while ensuring compliance with research protocols and regulatory...DataHourly payShift work3 days per week- Profound Research seeks a Clinical Research Coordinator II to manage assigned studies on-site, from start-up through... ...documentation and regulatory compliance. You will work directly with investigators... ...CROs to uphold patient safety and data integrity. The role emphasizes...Data
- ...Center (CUIMC) in New York is seeking a CRC III to support coordination of clinical research activities within the Surgery - Transplant Clinical... ...involves day-to-day monitoring, participant recruitment, data collection, and collaboration with clinicians and research...Data
- ...University Medical Campus is seeking a Clinical Research Coordinator I for Cardiology, supporting Cardio-... ...with sponsors, and ensure protocol compliance across all phases. Responsibilities include... ...participant recruitment, consent, data collection, and communicating...Data
- Phoenix Children's Hospital, Inc. is seeking a Research Coordinator to manage a range of clinical studies from initiation through closeout. You will coordinate... ...recruit and schedule participants, collect and enter data, and maintain accurate study records to support study...Data
- Moffitt Cancer Center is seeking a Clinical Research Coordinator I to support on-site clinical research activities at Magnolia Hospital. The CRC I... ...involves screening, enrolling and following study subjects, with data and AE reporting, and liaison duties among investigators,...Data
- ...Medical Center is seeking a detail-oriented Research Coordinator to assist in coordinating patient participation and data collection for clinical studies in a supportive academic... ...and scheduling, while ensuring protocol compliance and patient safety under supervision. A...Data
- 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... ...and annual reviews. Office support and data entry in REDCap may be required. #J-18808-Ljbffr...DataWork at office
- Description The Clinical Research Coordinator manages orthopaedic research studies from planning through completion. This position works... ...activities, recruit participants, manage and analyze data, and ensure compliance with study protocols and regulatory requirements. Key...DataLocal area
- Clinical Research Coordinator Department: Operations Employment Type: Full Time Location: Coastal Carolina... ...the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA Regulations... ...in source clinic charts; Entering data in EDC and answers queries;...DataFull timeTemporary work
- BeOne Medicines Ltd. is seeking a Regional Clinical Trial Management Associate to support... ...States. The role collaborates with Clinical Research Associates and Study Start-up... ...ensure quality, timelines, and budget compliance across country-level activities. The position...Remote job
- About Absci Absci is a clinical-stage biotechnology company... ...a synthetic biology data engine, enabling the... ...an experienced Clinical Trial Manager to independently... ...standards of quality, compliance, and efficiency. The Clinical... .... Oversee Contract Research Organizations (CROs)...DataContract workVisa sponsorshipWork visa
$131k - $181k
Adicet Bio, Inc. is a clinical stage biotechnology company... ...at . CLINICAL TRIAL MANAGER As a Clinical Trial... ...studies are conducted in compliance GCP/ICH, company... ...of 4 years of clinical research experience in biotechnology... ...studies in electronic data capture systems Experience...DataFull timeContract workTemporary workWork at officeFlexible hours3 days per week$90k - $150k
...with our FDA pivotal trial underway across 15... ...Charité, the Mayo Clinic, Duke, and Harvard... ...sites directly, coordinate the academic... ...our CMedO, Clinical Research Lead, regulatory,... ...backbone: eTMF, EDC, data cleaning, and protocol... ...and regulatory compliance (ISO 14155, MDR)...DataContract workWork at officeRemote workShift work$60.8k - $91.2k
Clinical Research Coordinator - Internal Medicine (All of Us) Department: SOM KC Internal Medicine - Administration All of Us Research... ..., screening, enrollment, biospecimen collection, data documentation, protocol compliance, and quality assurance activities. The CRC...DataFull timeWork experience placementLocal areaFlexible hoursAfternoon shift- # Clinical Trial Manager / Sr. (CTM) - NIS (Non-Interventional Studies)... ...deliverable (usually clean data from evaluable patients as specified... ...to high complexity, in compliance with ICH GCP. In accordance... ...wider management or project coordination responsibilities. • Develop...DataContract workWork at officeLocal area
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