73 Results for

Temporary Research Jobs in Oakley, OH

Jobs

Cincinnati, OH30+ days ago

Remote

Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol Communication with the medical site staff including coordinators, clinical research physicians, and their site staff Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements On-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site deviations/deficiencies and corrective/preventive actions to bring a site back into compliance and mitigate risks moving forward Verification that the investigator is enrolling only eligible subjects Regulatory document review Medical device and/or investigational product/drug accountability and inventory Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol Assess the clinical research site's patient recruitment and retention success and offering suggestions for improvement Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance. Must have a minimum of a Bachelor's degree in a health or science related field Experience as a Clinical Research Coordinator (minimum 1 year) Ability to travel 60-70% to locations nationwide is required; some visits may be conducted remotely Must maintain a valid driver's license and the ability to drive to monitoring sites Proficient knowledge of Microsoft Office Strong communication and presentation skills Must be detail-oriented and efficient in time management.

Cincinnati, Ohio30+ days ago

Remote

SOPs, GCP, and applicable regulatory requirements; On-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site deviations/deficiencies and corrective/preventive actions to bring a site back into compliance and mitigate risks moving forward; Verification that the investigator is enrolling only eligible subjects; Regulatory document review; Medical device and/or investigational product/drug accountability and inventory; Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol; Assess the clinical research site’s patient recruitment and retention success and offering suggestions for improvement; and. Responsibilities : Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol; Communication with the medical site staff including coordinators, clinical research physicians, and their site staff; Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per.

New!

Cincinnati, OH2 days ago

While the Principal Investigator is primarily responsible for the overall design, conduct, and management of the clinical trial, the CRC supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study. By performing these duties, the CRC works with the PI, department, sponsor, Lindner Center and institution to support and provide guidance on the administration of the compliance, financial, personnel and other related aspects of the clinical study.

Cincinnati, OH30+ days ago

Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol; Communication with the medical site staff including coordinators, clinical research physicians, and their site staff; Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements; On-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site deviations/deficiencies and corrective/preventive actions to bring a site back into compliance and mitigate risks moving forward; Verification that the investigator is enrolling only eligible subjects; Regulatory document review; Medical device and/or investigational product/drug accountability and inventory; Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol; Assess the clinical research site's patient recruitment and retention success and offering suggestions for improvement; and Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance. Must have a minimum of a Bachelor's degree in a health or science related field; Advanced degrees or prior clinical research experience is a plus; In-House CRA position available for those with no or minimal clinical research experience with rapid advancement; Ability to travel 60-70% to locations nationwide is required, or less if remote/virtual visits required; Must maintain a valid driver's license and the ability to drive to monitoring sites; Proficient knowledge of Microsoft® Office; Strong communication and presentation skills; and Must be detail-oriented and efficient in time management.

Cincinnati, OH30+ days ago

Clinical Research Nurse Sr • Bachelors Degree in Nursing • Current valid RN license to practice in the State of Ohio by date of hire • Two (2) years of clinical nursing experience in a hospital, clinic, or similar healthcare setting • At least two (2) years of clinical trials research experience. • Clinical Research Nurse • Associates Degree • Graduation from an accredited school of nursing • Current valid RN license to practice in the State of Ohio by date of hire • Two (2) years of clinical nursing experience in a hospital, clinic, or similar healthcare setting.

Cincinnati, OH30+ days ago

Home to more than 53,600 students, 12,000 faculty and staff, and over 360,000 living alumni, UC, a Carnegie 1 institution, combines research prowess with a physical setting that The New York Times has called the most ambitious campus design program in the country. As one of the oldest medical schools in the country, the University of Cincinnati College of Medicine, COM, has a reputation for training best-in-class healthcare professionals and developing cutting-edge procedures and research that improves the health and clinical care of patients.

Cincinnati, OH30+ days ago

As one of the oldest medical schools in the country, the University of Cincinnati College of Medicine (COM) has a reputation for training best-in-class health care professionals and developing cutting-edge procedures and research that improves the health and clinical care of patients. Accurately enters data from electronic medical records or paper research charts into study-specific electronic data capture systems in a timely manner for industry-sponsored, federally-funded, or investigator-initiated clinical research studies.

Cincinnati, Ohio30+ days ago

Responsibilities : Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol; Communication with the medical site staff including coordinators, clinical research physicians, and their site staff; Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements; On-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site deviations/deficiencies and corrective/preventive actions to bring a site back into compliance and mitigate risks moving forward; Verification that the investigator is enrolling only eligible subjects; Regulatory document review; Medical device and/or investigational product/drug accountability and inventory; Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol; Assess the clinical research site’s patient recruitment and retention success and offering suggestions for improvement; and. Qualifications : Must have a minimum of a Bachelor’s degree in a health or science related field; Advanced degrees or prior clinical research experience is a plus; In-House CRA position available for those with no or minimal clinical research experience with rapid advancement; Ability to travel 60-70% to locations nationwide is required, or less if remote/virtual visits required; Must maintain a valid driver’s license and the ability to drive to monitoring sites; Proficient knowledge of Microsoft® Office; Strong communication and presentation skills; and.

Cincinnati, OH30+ days ago

Full-time

Ensure consistency and effective communication during study visits and assure all procedures are conducted in compliance with the clinical protocol; Maintain subject safety, assess feedback from study participant and refer to investigators or other professionals as needed; If applicable, administer study medications based on state licensure, account for medications used . Create source templates for study documentation, complete case report forms, and other study specific documents seeking assistance from Senior Clinical Research Coordinator, Principal Clinical Research Coordinator, Team Leader or Clinical Site Director, as needed .

Cincinnati, OH30+ days ago

Full-time

Ensure consistency and effective communication during study visits; Assure all procedures are conducted in compliance with the clinical protocol; Maintain subject safety, assess feedback from study participant and refer to investigators or other professionals as needed; If applicable, administer study medications based on state licensure, account for medications used. Conduct clinical research in compliance with all applicable regulations; Request assistance and technical advice from Senior Clinical Research Coordinator, Principal Clinical Research Coordinator, Team Leader or Clinical Site Director, as needed.

Cincinnati, OH30+ days ago

Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol; Communication with the medical site staff including coordinators, clinical research physicians, and their site staff; Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements; Verification that the investigator is enrolling only eligible subjects; Regulatory document review; Medical device and/or investigational product/drug accountability and inventory; Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol; Assess the clinical research site's patient recruitment and retention success and offering suggestions for improvement; and Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance. 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 Americas 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.

Cincinnati, Ohio30+ days ago

Remote

Responsibilities : Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol; Communication with the medical site staff including coordinators, clinical research physicians, and their site staff; Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements; On-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site deviations/deficiencies and corrective/preventive actions to bring a site back into compliance and mitigate risks moving forward; Verification that the investigator is enrolling only eligible subjects; Regulatory document review; Medical device and/or investigational product/drug accountability and inventory; Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol; Assess the clinical research site’s patient recruitment and retention success and offering suggestions for improvement; and. Qualifications : Clinical Research Associate Experience (minimum 1 year); Ability to travel 60-70% to locations nationwide is required; Must have a minimum of a bachelor’s degree in a health or science related field; Proficient knowledge of Microsoft® Office; Strong communication and presentation skills; and.

Cincinnati, Ohio30+ days ago

Candidates must have at minimum a Bachelor’s degree in a health or science related field, minimum one year of clinical research experience or relevant direct industry experience (e.g., CRC), ability to travel nationwide, must be detail-oriented, strong time management, and communication skills. 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.

Cincinnati, OH30+ days ago

$55,000–$60,000 Per Year

Research Assistant will be responsible for translating system and client needs analysis and development into technical solutions by writing software applications, integrating systems, creating, modifying, and/or supporting desktop, web-based, mobile, cloud, and virtual applications, and application programming interfaces. The SoIT is home to several centers, including an NSADHS Center for Academic Excellence in Cyber Defense, the Information Technology Solutions Center, the Ohio Cyber Range Institute, Applied Machine Learning and Intelligence Center, and the Smart Synergies Lab.

cincinnati, OH30+ days ago

Competitive retirement plans Tuition reimbursement for continuing education Expansive employee discount programs through our many community partners Shift Differential, Weekend Differential, and Weekend Option Pay Programs for qualified positions Support through Employee Resource Groups such as African American Professionals Advisory Council, Asian Cultural and Professional Group, EQUAL - LGBTQA Resource Group, Juntos - Hispanic/Latin Resource Group, Veterans and Military Family Advocacy Network, and Young Professionals (YP) Resource Group Physical and mental health wellness programs Relocation assistance available for qualified positions Benefits may vary based on FTE Status and Position Type About Us At Cincinnati Children's, we come to work with one goal: to make children's health better. Service and/or Administration - Participates in program development for service and/or administration as evidenced by one of the following: make significant contributes to the development of a unique programs for patient care of educational purposes; or take a significant role in the direction of an academic division; or provide consultation on a specific program development; or significant participation in performance improvement programs or on divisional, departmental, or Medical Staff committees (i.e. RPT, IRB); participates in local or regional clinical affairs through membership in clinical societies or specialty governing boards.

Cincinnati, Ohio30+ days ago

Responsibilities : Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol; Communication with the medical site staff including coordinators, clinical research physicians, and their site staff; Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements; On-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site deviations/deficiencies and corrective/preventive actions to bring a site back into compliance and mitigate risks moving forward; Verification that the investigator is enrolling only eligible subjects; Regulatory document review; Medical device and/or investigational product/drug accountability and inventory; Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol; Assess the clinical research site’s patient recruitment and retention success and offering suggestions for improvement; and. Qualifications : Must have a minimum of a Bachelor’s degree in a health or life science related field; Ability to travel 60-70% to locations nationwide is required, or less if remote/virtual visits required; Must maintain a valid driver’s license and the ability to drive to monitoring sites; Minimum 1 year healthcare-related work experience preferred; Proficient knowledge of Microsoft® Office; Strong communication and presentation skills; and.

Cincinnati, OH30+ days ago

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. Named a Top Workplace in 2024 by The Cincinnati Enquirer Recognized by Forbes as one of Americas 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.

Cincinnati, OH30+ days ago

In this position, you will be working with a highly experienced team of other administrators and clinical research professionals that can help you grow your skillset while working for a growing and developing company. 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.

Cincinnati, OH30+ days ago

Completes study documentation and maintains study files in accordance with sponsor requirements and procedures including, but not limited to, consent forms, source documentation, narrative notes if applicable, case report forms, and investigational material accountability forms. Assists the Principal Investigator and Regulatory Specialist in submission of accurate and timely closeout documents to applicable federal agencies, and the sponsoring agency in accordance with federal regulations and sponsoring agency policies and procedures.

Cincinnati, OH30+ days ago

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Cincinnati, OH30+ days ago

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; • Coordinate project meetings and produce quality meeting minutes. 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.

Cincinnati, OH30+ days ago

Engage in clinical trial management on a day to day level; • Work closely with the project CTM for timely delivery of recurrent 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; • Coordinate project meetings and produce quality meeting minutes. 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.

Cincinnati, Ohio30+ days ago

Qualifications : BSN is required; 3+ years of Clinical Nurse experience required, research nurse experience preferred; Experience in Phases 1-4; Phases 2-3 preferred; Management of overall project timeline; Strong leadership skills. Job Summary: Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers with established Clinical Research Nursing backgrounds to join our Clinical Trial Management Group.

Cincinnati, Ohio30+ days ago

Responsibilities : Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol; Communication with the medical site staff including coordinators, clinical research physicians, and their site staff; Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements; Verification that the investigator is enrolling only eligible subjects; Regulatory document review; Medical device and/or investigational product/drug accountability and inventory; Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol; Assess the clinical research site’s patient recruitment and retention success and offering suggestions for improvement; and. Qualifications : Must have a minimum of a Bachelor’s degree in a health or science related field; degree in Physical Therapy or Kinesiology preferred; Ability to travel 60-70% to locations nationwide is required; Must maintain a valid driver’s license and the ability to drive to monitoring sites; Minimum 1 year healthcare-related work experience preferred; Proficient knowledge of Microsoft® Office; Strong communication and presentation skills; and.

Cincinnati, Ohio30+ days ago

Manage electronic filing system for trial documentation; Track, maintain, and perform quality check of electronic documents; Communicate with internal associates globally regarding errors in trial documents; and. In this position, you will be working with a highly experienced team of other administrators and clinical research professionals that can help you grow your skillset while working for a growing and developing company.

Cincinnati, OH30+ days ago

The research associate will be expected to assist with the preparation, coordination, and submission of research grant proposals, help manage grant correspondence and paperwork, help conduct research, collaborate with other members of the research team, and lead and support the dissemination of research projects. Hazards: Includes a variety of physical conditions such as proximity to moving mechanical parts of machinery or tools used to perform work, moving vehicles, electrical current, working on scaffolding and high places, or exposure to chemicals.

Cincinnati, Ohio30+ days ago

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. 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.

Cincinnati, Ohio30+ days ago

Responsibilities : Engage in clinical trial management on a day to day level; Work closely with the project CTM for timely delivery of recurrent 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. 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.

Cincinnati, Ohio30+ days ago

New!

Cincinnati, OH2 days ago

$20.57–$25.72 Per Hour

Assists in daily operations of the laboratory including answering phone, maintaining lab supplies, organization, and cleanliness. Assists in training students and new/junior laboratory personnel in laboratory techniques and equipment operation.

loveland, OH30+ days ago

We currently are seeking several quality, self-driven LPN's to work in In-Patient Clinical Research Studies at Cincinnati Children's Hospital Medical Center in Cincinnati, OH. We are offering a PRN opportunity on either day and night working on a clinical research study at Cincinnati Children's Hospital Medical Center.

loveland, OH30+ days ago

We currently are seeking several quality, self-driven RN's to work in In-Patient Clinical Research Studies at Cincinnati Children's Hospital Medical Center in Cincinnati, OH. We are offering a PRN opportunity on either day and night working on a clinical research study at Cincinnati Children's Hospital Medical Center.

Cincinnati, OH30+ days ago

Cincinnati, Ohio30+ days ago

Cincinnati, OH30+ days ago

cincinnati, OH30+ days ago

Cincinnati Children''s is: Recognized by U.S. News & World Report as a top 10 best children''s hospitals in the nation for more than 15 yearsSecond Among All Children''s Hospitals for National Institutes of Health (NIH) FundingRecognized as one of America's Best Large Employers (2025) , America's Best Employers for New Grads (2024)One of the nation''s America's Most Innovative Companies as noted by FortuneConsistently certified as great place to workA Leading Disability Employer as noted by the National Organization on DisabilityMagnet® designated for the fourth consecutive time by the American Nurses Credentialing Center (ANCC) JOB RESPONSIBILITIESTo provide safe and effective patient care. Support through Employee Resource Groups such as African American Professionals Advisory Council, Asian Cultural and Professional Group, EQUAL - LGBTQA Resource Group, Juntos - Hispanic/Latin Resource Group, Veterans and Military Family Advocacy Network, and Young Professionals (YP) Resource Group Physical and mental health wellness programs Relocation assistance available for qualified positionsBenefits may vary based on FTE Status and Position Type Primary LocationLocation B ScheduleFull time ShiftDay (United States of America) DepartmentAnesthesia Employee StatusRegular FTE1 Weekly Hours40 Comprehensive job description provided upon request.

Cincinnati, OH30+ days ago

Full-time

Members of UC Health include: UC Medical Center, West Chester Hospital, University of Cincinnati Physicians and UC Health Ambulatory Services (with more than 900 board-certified clinicians and surgeons), Lindner Center of HOPE and several specialized institutes including: UC Gardner Neuroscience Institute and the University of Cincinnati Cancer Center. Under the supervision of the Director of Pharmacy, the Clinical Pharmacy Specialist (CPS) provides specialized clinical pharmacy services to patients receiving care under the medical direction of a general or specialty department, division, or service, regardless of the physical location of the patient within the hospital or ambulatory clinics.

Cincinnati, OH30+ days ago

Full-time

Cincinnati, OH30+ days ago

Real Work-Life BalanceUC prioritizes work-life balance with a generous time-off policy includingVacation and sick time11 paid holidays and additional end-of-year paid time off Winter Season Days6 weeks of paid parental leave for new parentsAdditional Benefits IncludeCompetitive salary based on experienceComprehensive health coverage medical dental vision prescriptionFlexible spending accounts & wellness programsProfessional development & mentorship opportunitiesTo learn more about why UC is a great place to work please visit our careers page athttpswww.uc.educareers.html With world-class research teaching and medical practice opportunities why not choose the University of Cincinnati College of MedicineThe Department of Internal Medicine Division of Nephrology is recognized regionally and nationally for leading andor contributing to cutting-edge research and advancing the knowledge about kidney diseases to patients peers and trainees.

Cincinnati, OH23 days ago

$60.09–$83.87 Per Hour

Under the supervision of the Director of Pharmacy, the Clinical Pharmacy Specialist (CPS) provides specialized clinical pharmacy services to patients receiving care under the medical direction of a general or specialty department, division, or service, regardless of the physical location of the patient within the hospital or ambulatory clinics. Members of UC Health include: UC Medical Center, West Chester Hospital, University of Cincinnati Physicians and UC Health Ambulatory Services (with more than 900 board-certified clinicians and surgeons), Lindner Center of HOPE and several specialized institutes including: UC Gardner Neuroscience Institute and the University of Cincinnati Cancer Center.

Cincinnati, OH28 days ago

$60.09–$83.87 Per Hour

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Temporary Research Jobs in Oakley, OH

Clinical Research Coordinator to Home Based CRA (Clinical Research Associate) Medpace Holdings Inc

Clinical Research Associate - Clinical Research Coordinator Experience Medpace, Inc.

Clinical Research Coordinator II - MOB Lindner Research HV - Full Time - Days The Christ Hospital Health Network

Clinical Research Associate Cincinnati, OH (Entry Level) Medpace Holdings Inc

Clinical Research Nurse / Senior Clinical Research Nurse, UC Cancer Center University of Cincinnati

Clinical Research Professional / Clinical Research Professional II, UC Cancer Center University of Cincinnati

Clinical Research Assistant, Department of Obstetrics and Gynecology University of Cincinnati

Clinical Research Associate - Cincinnati, OH (Entry-Level) Medpace, Inc.

Clinical Research Coordinator (level dependent on experience) CTI Clinical Trial Services, Inc.

Clinical Research Nurse Coordinator CTI Clinical Trial Services, Inc.

Clinical Research Associate (Physical Therapist Candidates) Medpace Holdings Inc

Home-Based Experienced CRA (Clinical Research Associate)- Bonus/Equity Medpace, Inc.

Experienced Clinical Research Associate - Hematology/Oncology Medpace, Inc.

Sr. Research Assistant, Information Technology Solutions Center, School of Information Technology University of Cincinnati

Anesthesia - Director of Clinical and Translational Research Cincinnati Children's Hospital Medical Center

Clinical Research Associate (PhD Candidates) Medpace, Inc.

Clinical Trial Project Manager Research Nurses Medpace Holdings Inc

Clinical Research Documentation Administrator (TMF) Medpace Holdings Inc

Clinical Research Coordinator Gastro Health

Experienced Clinical Research Associate Hematology/Oncology Medpace Holdings Inc

Clinical Research Project Coordinator Cardiovascular, Renal, Metabolic Medpace Holdings Inc

Clinical Research Project Coordinator Immunology Medpace Holdings Inc

Clinical Research Project Coordinator Oncology Medpace Holdings Inc

Clinical Research Project Coordinator Gastrointestinal/GI Medpace Holdings Inc

Clinical Research Project Coordinator Infectious Disease Medpace Holdings Inc

Cincinnati Clinical Research Project Coordinator Medpace Holdings Inc

Clinical Trial Project Manager - Research Nurses Medpace, Inc.

Clinical Research Associate (Physical Therapist Candidates) Medpace, Inc.

Clinical Research Documentation Administrator (TMF) Medpace, Inc.

Research Associate, College of Pharmacy University of Cincinnati

Clinical Research Project Coordinator - Neuroscience Medpace, Inc.

Clinical Research Project Coordinator - Ophthalmology Medpace, Inc.

Cincinnati Clinical Research Project Coordinator Medpace, Inc.

Clinical Research Project Coordinator - Cardiovascular, Renal, Metabolic Medpace, Inc.

Clinical Research Project Coordinator - Oncology Medpace, Inc.

Clinical Research Project Coordinator - Infectious Disease Medpace, Inc.

Clinical Research Project Coordinator - Gastrointestinal/GI Medpace, Inc.

Clinical Research Project Coordinator - Immunology Medpace, Inc.

Research Assistant II - Ophthalmology - Owen Lab Cincinnati Children's Hospital Medical Center

LPN Clinical Research PRN CommonSpirit Health

RN Clinical Research Study PRN CommonSpirit Health

Entry Level Research Project Coordinator Medpace Holdings Inc

Entry-Level Research Project Coordinator Medpace, Inc.

Assistant / Assoc Professor, Clin Geo, Department of Neurology & Rehabilitation Medicine, General University of Cincinnati

Anesthesia - Associate Professor - Clinical Cincinnati Children's Hospital Medical Center

Med-Surg Float Clinical Pharmacy Specialist, First Shift, Inpatient Pharmacy, UCMC UC Health, LLC

Med-Surg Clinical Pharmacy Specialist, Second Shift, Inpatient Pharmacy, UCMC UC Health, LLC

Assistant / Associate or Professor, College of Medicine, Division of Nephrology University of Cincinnati

Transplant Clinical Pharmacy Specialist, First Shift Hybrid, Specialty Pharmacy UC Health

Clinical Pharmacy Specialist, Critical Care, First Shift, Inpatient Pharmacy UC Health

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