Clinical Trials & Research Coordinator
TriHealth
TriHealth is seeking an Academic Research Coordinator within the Hatton Research Institute to manage clinical trials focused on safety and regulatory excellence. This role involves collaboration with investigators, maintaining quality study data, and ensuring compliance with IRB/FDA standards. Responsibilities include developing research protocols, assessing potential subjects, and supporting staff. Qualifications include a Bachelor's in Science and 2-3 years of healthcare experience. Enjoy comprehensive benefits and a full-time schedule with no weekend or holiday commitments. #J-18808-Ljbffr TriHealth
- ...assist in study selection; correspond/coordinate with the sponsor/CRO; prepare study budgets. Prepare/manage site for clinical research studies, create study-specific source document... ...protocols for Investigator Initiated Trials. Conduct in-services for study staff,...SuggestedInterim roleWork at officeFlexible hours
$45k - $55k
Clinical Research Coordinator The Scientific Team at Pride health is hiring a DIRECT HIRE, Clinical Research Coordinator for an exciting oncology... ...Screens potential patients for protocol eligibility. Presents trial concepts and details to the patients, participates in the...SuggestedWork at officeLocal area- A leading clinical research organization in Cincinnati is seeking a Full-Time Clinical Research Coordinator to support clinical studies. This role offers a great work/life balance with no weekends or evenings, and includes a competitive compensation package. Responsibilities...SuggestedFull timeAfternoon shift
$24.46 - $26.23 per hour
Cincinnati Children's is seeking a Clinical Research Coordinator in Cincinnati, Ohio. The role involves maintaining project compliance, overseeing... ...study participants, and ensuring data integrity in clinical trials. Candidates should possess a high school diploma or...SuggestedHourly payFull time$24.46 - $26.23 per hour
Cincinnati Children's Office of Academic Affairs and Career Development is looking for Clinical Research Coordinators CRC II and CRC III. Candidates will manage clinical research studies, ensuring compliance with regulations and documentation. Qualified applicants should...SuggestedFull timeWork at office- A leading healthcare organization in Cincinnati is seeking a Full-Time Clinical Research Coordinator. The position offers a great work/life balance with no weekends or evenings. Responsibilities include coordinating clinical research activities, preparing regulatory documents...Full timeAfternoon shiftWeekday work
$24.46 - $26.23 per hour
A leading pediatric care provider in Cincinnati seeks dedicated Clinical Research Coordinators (CRC II/III). Responsibilities include coordinating studies, maintaining regulatory compliance, and managing participant recruitment. Candidates should have relevant experience...Hourly pay$56.78k - $62.15k
As a Clinical Research Coordinator in the Assa’ad Lab at Cincinnati Children’s, you will support clinical and translational studies focused on food... ...professionals in all aspects of conducting a clinical trial. Collaborate with investigator(s) and coworkers to ensure...Full timeWork experience placementShift work- TriHealth offers Clinical Research Coordinators a purpose‑driven career coordinating Phase II-IV clinical trials with a strong emphasis on safety, integrity, and high‑quality patient care, functioning as an educator, consultant, and liaison while collaborating closely with...Full timeReliefShift workDay shift
- A leading healthcare provider in Cincinnati is seeking a Clinical Research Coordinator. This role involves coordinating and managing clinical trials, with an emphasis on patient safety and regulatory compliance. The successful candidate will work closely with multidisciplinary...
- The University of Cincinnati is seeking a Clinical Research Professional to support clinical trials and coordinate treatment for patients. This role requires a Bachelor’s degree in a related field and either five years of relevant experience or more advanced qualifications...
$24.46 - $26.23 per hour
Job Responsibilities Study Conduct/ Clinical Research Practice - Maintain awareness of status of... ...all aspects of conducting a clinical trial. Collaborate with investigator(s) and coworkers... ...regulatory agencies, or consultants, & coordinate the process to meet these requirements....Full timeWork experience placementWork at office$24.46 - $26.23 per hour
Job Responsibilities Study Conduct / Clinical Research Practice - Assist in coordinating studies by preparing personnel and materials, preparing protocols, informed consents, amendments, and other necessary documents for review by the IRB and Sponsor. Assemble lab kits...Full timeWork experience placementLocal areaShift work- Gastro Health is seeking a Full-Time Clinical Research Coordinator to join our team! Gastro Health is a great place to work and advance in your career... ...or Administrative Knowledge Prior knowledge of clinical trials, as well as ICH-GCP principles, preferred Facilitation of...Full timeLocal areaMonday to FridayAfternoon shift
- A children's healthcare institution in Cincinnati is seeking a Clinical Research Coordinator to support clinical and translational studies on food allergies. Responsibilities include maintaining study status, ensuring regulatory compliance, handling participant recruitment...Full time
- A leading gastroenterology group based in Cincinnati, Ohio, is seeking a Full-Time Clinical Research Coordinator. In this role, you will coordinate clinical research activities and ensure adherence to federal regulations. Candidates must possess strong clinical research...Full time
$24.46 - $26.23 per hour
Job Responsibilities Study Conduct / Clinical Research Practice: Assist in coordinating studies by preparing personnel and materials, reviewing protocols, informed consents, amendments, and other necessary documents for IRB and sponsor review. Assemble lab kits, gather...Full timeWork experience placementWork at officeLocal areaShift work- ...are currently seeking a full-time, office-based Project Coordinator to join our Clinical Trial Management team. This position will work on a team to... ...fast paced, collaborative work environment in clinical research and want to develop your career even further, then this...Full timeContract workWork at officeLocal areaImmediate startFlexible hours
- ...A leading consulting firm is seeking a Clinical Project Manager III to oversee clinical trials' execution and ensure compliance with ICH guidelines. The ideal... ...allied health fields and at least 6 years of clinical research experience. Responsibilities include managing...Remote work
- ...Clinical Project Manager III/ Senior (level dependent on experience... ...oversight of assigned clinical trials (Phase I through Phase IV) to... .... Provide oversight and coordination of the operational aspects of... ...Provide oversight of Clinical Research Associate (CRA) tasks on assigned...Full timeContract workWork experience placementRemote workWork from homeRelocation package
- ...Clinical Trial Manager Medpace is the leading CRO for Biotech companies and is continuing to add established Clinical Trial Managers... ...site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables. Qualifications...Contract workWork at officeLocal areaImmediate startFlexible hours
- ...Senior Clinical Project Manager – Oncology/Hematology (Phase III) (Remote – US/Canada)Are... ...about advancing oncology and hematology research? Do you thrive in a fast-paced, collaborative... ...and take ownership of complex Phase III trials, driving projects from proposal through...Contract workRemote work
- A biopharmaceutical company is seeking a full-time Study Coordinator to join their Clinical Pharmacology Unit in Cincinnati, Ohio. This role involves working on a team to manage study subjects, ensure safe medication administration, and assess adverse events. Candidates...Full timeWork at office
- Job Summary Medpace Clinical Pharmacology, a 96-bed facility specializing in early phase clinical trials, is led by a team of highly trained clinical researchers who are experts in the design, implementation... ...to Sponsor specifications; Coordinate project start-up, maintenance...
- A global clinical trial organization in Cincinnati is looking for a Global Project Manager to oversee laboratory clinical trials. The role involves planning, executing, and managing projects while ensuring compliance with international guidelines and budget oversight....
- A leading clinical trial organization in Covington, Kentucky is seeking an experienced project manager for laboratory clinical trials.... ...ensuring adherence to ICH guidelines and GCP. This role involves coordinating project deliverables, managing budgets, and fostering team...
- ...Associate Clinical Trial Manager Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience related to Ophthalmology for a full-time, office-based... ...Management team working with Project Coordinators and Clinical Trial Managers in...Full timeContract workWork at officeLocal areaImmediate startFlexible hours
$65k - $80k
...organization is seeking an Oncology Research Registered Nurse (RN) for a direct hire... ..., OH. Responsibilities include coordinating patient trials, ensuring compliance with protocols,... ...licensure, and two years of relevant clinical research or oncology experience. The...- Medpace is hiring an Associate Clinical Trial Manager in Cincinnati, Ohio. This full-time role seeks PhDs or Post-Doctoral candidates in Life Sciences, focusing on project management in clinical trials. Responsibilities include collaborating on global study activities...Full timeFlexible hours
- A leading clinical research organization is seeking an Associate Clinical Trial Manager in Cincinnati, Ohio. This role is designed for recent PhD graduates looking to launch their career in clinical project management, providing foundational training and opportunities for...
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