Clinical Research Manager
PRISM Vision Group
Clinical Research ManagerPosition: Clinical Research ManagerWeekly Hours: 40 (full time)Responsible for ensuring at the administrative level that all research activities are coordinated with affected departments within the practice. Coaches and develops staff. Collaborates in the development of research accountability standards and identifies areas for improvement. Ensures site research quality by practicing in compliance with US Oncology Research, Inc. (USOR) Standard Operating Procedures (SOP), principles of Good Clinical Practice (GCP) and applicable federal, state, and local regulations. Supports and adheres to the US Oncology Compliance Program, to include Code of Ethics and Business Standards.Why choose OHC?You take care of our patients, so we take care of you. OHC's benefits include:3 Health Insurance Plans to choose from2 Dental and 2 Vision insurance plansA company 401K planProfit sharing plan for clinical employeesCompetitive salariesCompany paid short term / long term disability / life insurancePaid HolidaysA generous PTO planTuition ReimbursementProfessional Development ProgramNationwide Discounts at your favorite hotels, resorts and retailers just for being an OHC employeeWellness ProgramPeriodic merit raisesOpportunities for advancementAbout the company: OHC has served as the region's premier provider of treatments for cancer and blood disorders, offering a wide range of services and state-of-the-art treatments and technologies, as well as being nationally recognized for cutting edge clinical research breakthroughs in Southwest Ohio area for over 40 years. Serving patients close to home through our Cancer Centers of Excellence in Fairfield, West side of Cincinnati, Blue Ash, Kenwood and Eastgate in Ohio. OHC puts patients first by delivering compassionate and convenient care, tailored to meet a patient's medical and personal needs.ResponsibilitiesKey ResponsibilitiesSupervises clinical research staff members in accordance with USOR SOP and ICH GCP guidelines. Responsible for ensuring at the administrative level that all research activities are coordinated with affected departments within the practice.Coaches and develops staff. Participates in the recruitment, interviewing, hiring, assessing performance, recommending salary changes, and progressive discipline. Enforces adherence to company policies.Collaborates in the development of research accountability standards, metrics, and reports and identifies areas for improvement. Collaborates with site research leader (SRL), upper management, and staff in the implementation of action plans designed to improve practice research operations and quality assurance functions.Collaborates with the SRL, physicians of the practice, and other research management in the process of study selection for the research program.Collaborates with SRL and upper management on the development of research budgets, financial objectives, and accrual targets.May promote or market research program to the practice, community, and referring physicians.May coordinate research activities with other (non-USOR) bases or sponsors.QualificationsMinimum Job Qualifications (Knowledge, Skills, & Abilities):Education/Training –Associates degree in a clinical or scientific related discipline requiredGraduate of an accredited nursing program preferredBusiness Experience -Minimum 5 years clinical nursing experience or scientific related discipline required, preferably in oncologySupervisory experience preferred, experience in clinical research preferredIf required in state of practice, current licensure as a registered (RN)Current BCLS or ACLS certification for nursesSoCRA or ARCP certification preferredSpecialized Knowledge/Skills -Excellent communication skillsStrong ability to multitask, strong interpersonal skillsMust be able to work in a fast-paced, constantly changing environmentKnowledge and proficiency in all basic computer programs, Windows, Excel, etc.Special knowledge of GCP and ICH guidelines preferredKnowledge of medical terminology, nursing assessment, clinical medicine, diagnostic tests, radiology, pathology, pharmacology, hematology, oncology as it relates to clinical trials
- OHC is seeking a Clinical Research Manager to oversee administrative coordination of research activities across departments. The role includes coaching staff, ensuring quality, and maintaining compliance with USOR SOPs, GCP, and applicable regulations. You will support...Suggested
- ...Clinical Research Project Manager, COM CCTST Posting Start Date: 8/27/26 Work Arrangement: Hybrid Current UC employees must apply internally via SuccessFactors Next Lives at the University of Cincinnati Founded in 1819, the University of Cincinnati ranks...SuggestedHourly payFull timeWork experience placementFlexible hours
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$74.3k - $94.74k
...based on FTE status. Job Responsibilities Clinical Operations - Provide direct supervision... ...and interdepartmental grant and research projects. People Planning - Conduct ongoing... ...Work with faculty, and business director/managers to provide leadership for new project development...SuggestedFull timeContract workWork experience placementLocal areaShift workWeekend work- ...Medical Laboratory Scientist to provide day-shift leadership in a CAP-certified lab at the Burnet Campus. You will collect and analyze clinical data, ensure high-quality testing, and support staff development within a 40-hour week. The role requires a bachelor’s degree or...Work at officeDay shift
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- ...Clinical Research Coordinator IIThe Clinical Research Coordinator II conducts and manages multiple clinical trials from start up through study close out in accordance with the study protocol, GCP, and Velocity's SOPs.ResponsibilitiesDuties/Responsibilities:Conduct and...Work at officeFlexible hours
- ...Clinical Research CoordinatorTriHealth 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...Full timeShift work
- ...for Biotech companies and we are currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will be a part of the Clinical Trial...Full timeContract workWork at officeWork from home
$90k - $143k
Job Title Clinical Partnership Manager - Pediatrics (Cincinnati, OH) Job Description The Clinical Partnership Manager - Pediatrics leads clinical... ...accommodation for this position. Certified Clinical Research Professional (CCRP) Advanced MRI certification or pediatric...Full timeWork at officeImmediate startWork visaRelocation package3 days per week$56.78k - $62.15k
...apply. Annual pay may vary based on FTE status. Join Our Clinical Research Coordinator Talent Community Cincinnati Children's is seeking... ...recruitment and enrollment, conduct study visits, manage regulatory documentation, collect and process research specimens...Full timeWork experience placementWork at officeShift workWeekend work$24.46 - $27.73 per hour
...based on FTE status. JOB RESPONSIBILITIES Study Conduct/ Clinical Research Practice - Assist in coordinating studies by preparing... ...sponsors, coordinating centers, study coordinators, clinical team, managers and other institutions. Maintain relationship with...Full timeWork experience placementLocal areaShift workWeekend work- Clinical Research Coordinator (level dependent on experience) Job Category : Clinical Research Center Requisition Number : CLINI001988 Posted : August 20, 2026 Full-Time On-site Locations Showing 1 location Clinical Research Center Cincinnati, OH Description Coordinate...Full timeLocal areaWork from home
- Cincinnati Children's is seeking Clinical Research Coordinators to support innovative clinical and translational research programs across multiple... ...recruitment and enrollment, conduct study visits, manage regulatory documentation, collect and process specimens, oversee...
$74.3k - $94.74k
...Division of Developmental and Behavioral Pediatrics conducts clinical research focused on improving outcomes for children with ADHD and... ...operations, regulatory compliance, participant engagement, data management, and study execution. This role will also serve as a key...Full timeLocal areaShift workWeekend work- ...TriHealth offers Clinical Research Coordinators a purpose-driven career coordinating Phase II-IV clinical trials with a strong emphasis on... ...Healthcare Providers (BLS) Job Overview: Coordinates and manages all components required for an organized multi-disciplinary team...Full timeReliefShift workDay shift
- ...Relationship Coordinator is a new role within the Clinical Monitoring team at Medpace that offers... ...to have an exciting career in the research of drug and medical device development.... ...within assigned country; Support Management in conducting/expediting feasibility activities...Full timeContract workWork at officeWork from home
- Senior Clinical Project Manager - up to $15K sign-on bonus! Job Category : Clinical Project Mgmt Requisition Number : CLINI001630 Apply now Posted... ...and relevant work experience At least 6 years of clinical research experience at a CRO or possesses transferrable skills and...Remote jobFull timeContract workWork experience placementWork from homeRelocation package
- TriHealth's Good Samaritan Hospital in Cincinnati, OH is seeking a Clinical Research Coordinator. The role oversees coordination of multi-disciplinary teams to execute Phase II-IV clinical trials with a focus on safety, integrity, and protocol compliance. The incumbent...
- Ctifacts is seeking a Clinical Research Coordinator for our Cincinnati, OH site. The role encompasses coordinating Phase I-IV studies following GCPs, SOPs, and regulatory standards. You will manage study visits, consent, data collection, and drug accountability while maintaining...
- ...a full-time, office-based Project Coordinator to join our Clinical Trial Management team. This position will work on a team to accomplish tasks... ...a fast paced, collaborative work environment in clinical research and want to develop your career even further, then this is...Full timeContract workWork at officeWork from home
- CTI Clinical Trial and Consulting Services in Cincinnati seeks a Clinical Research Coordinator to coordinate Phase I through IV studies in line with GCPs, ICH guidelines, and SOPs, from pre-study planning to the final study visit. You’ll recruit volunteers, prepare study...
- Velocity Clinical Research, Inc. is seeking a Clinical Research Coordinator II to oversee multiple trials from initiation to close-out in... ...Responsibilities include start-up coordination, subject recruitment, data management, and safety reporting. The role requires strong medical...Work at office
- Clinical Project Manager III/ Senior (level dependent on experience) Join to apply for the Clinical Project Manager III/ Senior (level dependent... ...execution of the protocol. Provide oversight of Clinical Research Associate (CRA) tasks on assigned projects; provide oversight...Full timeContract workWork experience placementWork from homeRelocation package
$24.46 - $27.73 per hour
...Ophthalmology staff member at the Burnet Campus. This role supports clinical research activities within the Ophthalmology department, including protocol coordination, consent processes, and data management. Starting pay is available, with range $24.46-$27.73 per hour. Pay...Hourly payFull time- Medpace, a leading life sciences CRO headquartered in Cincinnati, seeks an entry-level Research Coordinator to develop a foundational understanding of clinical research under physician and scientist mentorship. You will gain exposure to Good Clinical Practice, assist in...
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