Clinical Research Project Coordinator - Cardiovascular, Renal, Metabolic
Medpace, Inc.
Job Summary Medpace is a leading CRO for Biotech companies and we 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 accomplish tasks and projects that are instrumental to the company’s success. Our therapeutic areas of focus include Microbiology, Oncology/Hematology, Cardiovascular/Metabolic/Renal, Infectious Disease/CNS/Ophthalmology and more. If you are looking for a fast paced, collaborative work environment in clinical research and want to develop your career even further, then this is the opportunity for you. Medpace provides Project Coordinators a 4-6 week training program that incorporates a virtual and hands on learning experience, especially for those without previous clinical research experience. Responsibilities Engage in clinical trial management on a day to day level; Work closely with the project CTM for timely delivery of tasks consistently with a high degree of accuracy; Compile and maintain project-specific status reports; Interact with the Sponsor, study sites, and internal associates; Provide oversight and quality control of our internal regulatory filing system; Manage study supplies; Create and maintain project timelines; and Coordinate project meetings and produce quality meeting minutes. Qualifications Minimum of a Bachelor’s Degree in Life Sciences field; Excellent computer, organizational, and time management skills; and Research experience preferred. Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Cincinnati Perks Cincinnati Campus Overview Flexible work environment Competitive PTO packages, starting at 20+ days Competitive compensation and benefits package Company-sponsored employee appreciation events Employee health and wellness initiatives Community involvement with local nonprofit organizations Discounts on local sports games, fitness gyms and attractions Modern, ecofriendly campus with an on-site fitness center Structured career paths with opportunities for professional growth Discounted tuition for UC online programs Awards Named a Top Workplace in 2024 by The Cincinnati Enquirer Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What to Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. #J-18808-Ljbffr
- ...continuing to add established Clinical Trial Managers and Project Managers with a focus on Cardiovascular, Renal, and Gastrointestinal... ...supervision of project Clinical Research Associates and monitoring... ...oncology, cardiology, metabolic disease, endocrinology, central...SuggestedContract workLocal areaImmediate startFlexible hours
- ...Science areas, working within Cardiovascular, Nephrology / Renal or Gastrointestinal (GI), Endocrine, and Metabolic research areas. This event is an... ...from academia to the Clinical Trials Industry.... ...will work closely with Project Coordinators and Clinical Trial Managers...SuggestedFull timeWork at officeLocal areaFlexible hours
- ...Medpace is hiring an Associate Clinical Trial Manager (aCTM) in Cincinnati, offering a chance for recent PhD graduates. The role includes supporting project management activities, collaborating with interdisciplinary teams, and ensuring accuracy in project tasks. Candidates...SuggestedFlexible hours
- ...Clinical Research Coordinators Wanted At Medpace Clinical Research Coordinators wanted at Medpace! Become a CRA and join our growing team!... ...expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-...SuggestedContract workWork at officeLocal areaImmediate startRemote workWork from homeHome officeFlexible hours
- ...AND RESPONSIBILITIES Evaluate protocols; 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 binders for each subject including appointment...SuggestedInterim roleWork at officeFlexible hours
- ...Job Responsibilities Study Conduct/ Clinical Research Practice - Maintain awareness of status... ...regulatory agencies, or consultants, & coordinate the process to meet these requirements... ...management process for clinical research projects, including addressing data queries...
- ...Job Summary Medpace Clinical Pharmacology, a 96-bed... ...trained clinical researchers who are experts in the... ...managing one or more projects according to Sponsor specifications; Coordinate project start-up, maintenance... ...oncology, cardiology, metabolic disease, endocrinology...Contract workLocal areaImmediate startFlexible hours
- ...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...
- ...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
$24.46 - $27.73 per hour
...Job Responsibilities Assist in coordinating studies by preparing personnel and materials, preparing... ...logged, handled and stored. Follow direction of clinical research coordinator or others involved in the clinical research project work. Assist other staff members and...Full timeWork experience placementLocal areaShift work$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... ...Research Clinic and Food Allergy Clinic, you’ll contribute to projects that address health disparities, refine diagnostic...Full timeWork experience placementShift work- ...The University of Cincinnati is looking for a Clinical Research Professional I or II in the Department of Radiology. This full-time position involves planning and coordinating clinical research projects and ensuring compliance during studies. Qualified candidates will...Full time
- ...Cincinnati Children's Office of Academic Affairs and Career Development is seeking an individual to assist in coordinating clinical research studies. Responsibilities include managing protocols, participant recruitment, and ensuring regulatory compliance. Candidates should...Full timeWork at office
- ...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...Full timeReliefShift workDay shift
- ...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
- ...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... ...all key personnel or persons ‘engaged’ in the research project have met training requirements in accordance with federal...Full timeLocal areaMonday to FridayAfternoon shift
- ...Clinical Research Coordinator Specialized research professional working with and under the direction of the Principal Investigator (PI) and the Lindner Center for Research and Education. While the Principal Investigator is primarily responsible for the overall design...Full time
- 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...Full time
- ...medical procedures. Must be licensed and certified, with strong communication skills and a commitment to culturally relevant care. Experience in cardiovascular services is preferred, along with a professional demeanor in a team-oriented environment. #J-18808-Ljbffr...
- ...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 Purpose/ Summary The Clinical Project Manager III/ Senior is responsible for execution and... .... Provide operational oversight and coordination across functional teams and regions to... ...experience At least 6 years of clinical research experience (CRO CRA or Research...Work experience placement
- ...Senior Clinical Project Manager – Oncology/Hematology (Phase III) (Remote – US/Canada) Are you a seasoned CRO project leader passionate about advancing oncology and hematology research? Do you thrive in a fast‑paced, collaborative environment where your leadership directly...Contract workRemote work
- ...Project Assistant Our imaging services are growing rapidly, and we are currently... ...Medpace is a full-service clinical contract research organization (CRO). We provide Phase... ...areas including oncology, cardiology, metabolic disease, endocrinology, central nervous...Full timeContract workWork at officeLocal areaImmediate startFlexible hours
- ...Project Assistant Our laboratory activities are... ...management team and assisting clinical sites for one or more... ...related questions. Coordinate and provide minutes... ...clinical contract research organization (CRO). We... ...oncology, cardiology, metabolic disease, endocrinology...Full timeContract workLocal areaImmediate startFlexible hours
- 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. Ideal...
- A leading clinical trial organization in Covington, Kentucky is seeking an experienced project manager for laboratory clinical trials. The candidate will manage medium to... ...ICH guidelines and GCP. This role involves coordinating project deliverables, managing budgets, and...
- ...sector. This role is ideal for individuals who want to grow into Project Management by working directly alongside experienced PMs and... ...‑on exposure to project planning, field operations, equipment coordination, and client communication while supporting the safe and...For subcontractorWork at officeRelocation
$65k - $80k
...healthcare organization is seeking an Oncology Research Registered Nurse (RN) for a direct hire... ..., OH. Responsibilities include coordinating patient trials, ensuring compliance with... ...licensure, and two years of relevant clinical research or oncology experience. The role...- ...time, office-based Imaging Project Coordinator to join our team. If you want... ...Engineering Prior research related experience is preferred... ...Medpace is a full-service clinical contract research organization... ...including oncology, cardiology, metabolic disease, endocrinology,...Full timeContract workWork at officeLocal areaImmediate startFlexible hours
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