Top 131 Clinical research coordinator Jobs in Ohio

Clinical Research Coordinator II
Care Access —Lima, OH
- $60,000 - $90,000 a year
- Microsoft Word
- Spanish
- Patient monitoring
- Health savings account
- Paid holidays
Quick Apply
Clinical Research Nurse Coordinator
Cleveland VA Medical Research & Education Foundation —Cleveland, OH
- $75,000 - $90,000 a year
- Full-time
- Nursing
- Patient monitoring
- Customer service
- Health insurance
- Dental insurance
Quick Apply
Clinical Research Coordinator
Tekton Research Inc —New Carlisle, OH
- Monday to Friday
- Nursing
- Laboratory experience
- High school diploma or GED
Quick Apply
9d
Clinical Research Assistant II-Psychiatry
The Ohio State University Wexner Medical Center —Columbus, OH
- Online Application
- Background check
- Psychiatry
- Computer literacy
1d
Assistant Clinical Research Coordinator
Dermatologists of Central States —Canal Winchester, OH
- $18 - $22 an hour
- Nursing
- Microsoft Excel
- Vital signs
- Health insurance
- Dental insurance
Quick Apply
Early Career Clinical Research Opportunities
Medpace, Inc. —Cincinnati, OH
- Full-time
- Office
- Bachelor's degree
- In-person
- Free parking
- Health insurance
Clinical Research Coordinator II
Velocity Clinical Research, Inc. —Cincinnati, OH
- Full-time
- English
- Mid-level
- High school diploma or GED
- Paid holidays
- Health insurance
Quick Apply
Clinical Coordinator (RN) - OB
Avita Health System —Galion, OH
- Part-time
- RN License
- Hospital
- Mid-level
- Free parking
- Paid parental leave
Quick Apply
Clinical Research Study Coordinator
Intrepid Research —Cincinnati, OH
- $25 - $35 an hour
- Full-time
- Mid-level
- 3 years
- Bachelor's degree
- Health savings account
- Health insurance
Quick Apply
Respiratory Therapy Clinical Coordinator
University Hospitals —Willoughby, OH
- $35.62 - $55.72 an hour
- Full-time
- Acute care
- PALS Certification
- Hospital
- Tuition reimbursement
- Paid time off
Clinical Nurse Research Specialist I-Medical Oncology
University Hospitals —Cleveland, OH
- $62,629 - $97,947 a year
- Nursing
- RN License
- BLS Certification
Clinical Research Coordinator III (RN) *Sign On Bonus*
American Oncology Network, Inc. —Columbus, OH
- $26.54 - $49.29 an hour
- Full-time
- Nursing
- Microsoft Outlook
- RN License
Quick Apply
7d
Clinical Research Coordinator II–Lead CRC
Neurology Diagnostics, Inc. —Dayton, OH
- From $27 an hour
- Full-time
- Vital signs
- RN License
- Mid-level
- Health insurance
- Dental insurance
Quick Apply
Clinical Research Coordinator- Cardiovascular Medicine
The Ohio State University Wexner Medical Center —Columbus, OH
- Weekends as needed
- Background check
- Internal Medicine
- Pass drug screening
7d
Clinical Research Coordinator-Endocrinology, Diabetes and Metabolism
The Ohio State University Wexner Medical Center —Columbus, OH
- Online Application
- Background check
- Pass drug screening
- Mid-level
4d
Clinical Research Assistant-Medical Oncology
The Ohio State University Wexner Medical Center —Columbus, OH
- Online Application
- Background check
- Pass drug screening
- University
2d
Clinical Research Assistant II-Psychiatry
The Ohio State University —Columbus, OH
- Full-time
- Background check
- Psychiatry
- Computer literacy
Clinical Research Coordinator I - RI Biobeh Fox
Nationwide Children's Hospital —Columbus, OH
- Weekends as needed
- Word processing
- Writing skills
- Analysis skills
3d
Research Associate- RI Clinical & Translational (Kerlin)
Nationwide Children's Hospital —Columbus, OH
- Full-time
- Computer literacy
- Ability to climb stairs
- Master's degree
Clinical Research Coordinator I - RI Behav Trials Off
Nationwide Children's Hospital —Columbus, OH
- Weekends as needed
- Hospital
- Word processing
- Writing skills

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Clinical Research Coordinator II

Care Access -
Lima, OH

Quick Apply

Job Details

$60,000 - $90,000 a year

Benefits

Health savings account
Paid holidays
Disability insurance
Health insurance
Dental insurance
Flexible spending account
Paid time off
Vision insurance
401(k) matching

Qualifications

Microsoft Word
Computer operation
Writing skills
IVR
Collecting samples for laboratory testing
Clinical data entry
Research regulatory compliance
Clinical quality assurance standards
Medical terminology

Full Job Description

About Care Access

Care Access is working to make the future of health better for all. With hundreds of research locations, mobile clinics, and clinicians across the globe, we bring world-class research and health services directly to communities that often face barriers to care. We are dedicated to ensuring that every person has the opportunity to understand their health, access the care they need, and contribute to the medical breakthroughs of tomorrow.

With programs like Future of Medicine, which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. Through partnerships, technology, and perseverance, we are reimagining how clinical research and health services reach the world. Together, we are building a future of health that is better and more accessible for all.

To learn more about Care Access, visit www.CareAccess.com.

How This Role Makes a Difference

The Clinical Research Coordinator's primary responsibilities are to utilize Good Clinical Practices (GCP)s in the process of screening, enrolling and closely monitoring clinical research study subjects while ensuring protocol and regulatory compliance.

How You'll Make An Impact

Duties include but not limited to:
- Ability to understand and follow institutional SOPs.
- Review and assess protocol (including amendments) for clarity, logistical feasibility
- Ensure that all training and study requirements are met prior to trial conduct.
- Discuss study medication, required procedures, eligibility criteria and impact on office flow with Investigator and site staff.
- Assist with planning and creation of appropriate recruitment materials
- Assist in development of recruitment plan and obtain listing of potential candidates to contact from subject database.
- Actively work with recruitment team in calling and recruiting subjects
- Attend Investigator meetings as required.
- Coordinate and attend pre-study site visits, site initiation visits, and monitor visits with clinical staff and Sponsor/CRO representatives.
- Assist in the creation and review of source documents.
- Ensure adequate supplies have arrived on site for protocol initiation (lab kits, study medication, specialized equipment, IVRS/EDC access and passwords)
Study Management
- Prioritize activities with specific regard to protocol timelines
- Maintain adherence to FDA regulations and ICH guidelines in all aspects of conducting clinical trials
- Maintain effective relationships with study participants and other care Access Research personnel.
- Interact in a positive, professional manner with patients, sponsor representatives, investigators and Care Access Research personnel and management.
- Communicate clearly verbally and in writing.
Patient Coordination
- Prescreen study candidates
- Obtain informed consent per Care Access Research SOP
- Complete visit procedures in accordance with protocol.
- Train others and complete basic clinical procedures, such as blood draws, vital signs, ECGs, etc.
- Review laboratory results, ECGs, and other test results (e.g., MRIs) for completeness and alert values, ensuring investigator review in a timely fashion.
- Identify adverse events (AEs) and Serious Adverse Events (SAEs) and promptly notify Principal Investigator and Sponsor (where appropriate)
Documentation
- Record data legibly and enter in real time on paper or e-source documents
- Accurately record study medication inventory, medication dispensation, and patient compliance.
- Resolve data management queries and correct source data within sponsor provided timelines
- Assist regulatory personnel with completion and filing of regulatory documents.
- Perform other duties as assigned. The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive.

The Expertise Required

Excellent working knowledge of medical and research terminology
Excellent working knowledge of federal regulations, good clinical practices (GCP)
Ability to communicate and work effectively with a diverse team of professionals.
Strong organizational, prioritization and leadership skills and capabilities with a strong attention to detail
Strong computer skills with demonstrated abilities using clinical trials database, IVR systems, electronic data capture, MS word and excel.
Critical thinker and problem solver
Friendly, outgoing personality; maintain a positive attitude under pressure.
High level of self-motivation and energy
Excellent professional writing and communication skills
Ability to work independently in a fast-paced environment with minimal supervision.

Certifications/Licenses, Education, and Experience:

Minimum Education:
- Bachelor's Degree preferred, or equivalent combination of education, training and experience.
Minimum Experience:
- 3 years prior Clinical Research Coordinator experience required
- Prefer 1 year of experience as a Care Access Research Clinical Research Coordinator
- Recent phlebotomy experience required
Bilingual in Spanish preferred

How We Work Together

Location: This is an on-site position with regional commute requirements. Position requires onsite work 5 days per week at the Lima, OH clinic.
Travel: Regularly planned travel within the region will be required as part of the role.
Physical demands associated with this position Include: The ability to use keyboards and other computer equipment.

The expected pay range for this role is $60,000 - $90,000 USD per year for full time team members.

Benefits & Perks (US Full Time Employees)

Paid Time Off (PTO) and Company Paid Holidays
100% Employer paid medical, dental, and vision insurance plan options
Health Savings Account and Flexible Spending Accounts
Bi-weekly HSA employer contribution
Company paid Short-Term Disability and Long-Term Disability
401(k) Retirement Plan, with Company Match

Mandatory Employer Disclosures:
Notice to Illinois applicants: Applicants are not obligated to disclose expunged juvenile records or adjudication, arrest, or conviction.
Notice to Connecticut applicants: Care Access may require applicants to submit to a urinalysis drug test in connection with an application for employment.
Notice to Arizona, Georgia, Indiana, and North Dakota applicants: Care Access complies with applicable laws prohibiting smoking in and around places of employment.
Notice to Massachusetts applicants: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
Notice to Rhode Island applicants: Care Access complies with Rhode Island law prohibiting smoking in enclosed areas within places of employment. Care Access is also subject to is subject to Chapters 29–38 of Title 28 of the Rhode Island General Laws.
Notice to Maryland applicants: UNDER MARYLAND LAW, AN EMPLOYER MAY NOT REQUIRE OR DEMAND, AS A CONDITION OF EMPLOYMENT, PROSPECTIVE EMPLOYMENT, OR CONTINUED EMPLOYMENT, THAT AN INDIVIDUAL SUBMIT TO OR TAKE A LIE DETECTOR OR SIMILAR TEST. AN EMPLOYER WHO VIOLATES THIS LAW IS GUILTY OF A MISDEMEANOR AND SUBJECT TO A FINE NOT EXCEEDING $100.

Diversity & Inclusion

We work with and serve people from diverse cultures and communities around the world. We are stronger and better when we build a team representing the communities we support. We maintain an inclusive culture where people from a broad range of backgrounds feel valued and respected as they contribute to our mission.

We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to, and will not be discriminated against on the basis of, race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law.

Care Access is unable to sponsor work visas at this time.

If you need an accommodation to apply for a role with Care Access, please reach out to: [email protected]

Quick Apply

Refine Your Search

clinical research coordinator jobs in ohio

Clinical Research Coordinator II

Clinical Research Nurse Coordinator

Clinical Research Coordinator

Clinical Research Assistant II-Psychiatry

Assistant Clinical Research Coordinator

Early Career Clinical Research Opportunities

Clinical Research Coordinator II

Clinical Coordinator (RN) - OB

Clinical Research Study Coordinator

Respiratory Therapy Clinical Coordinator

Clinical Nurse Research Specialist I-Medical Oncology

Clinical Research Coordinator III (RN) Sign On Bonus

Clinical Research Coordinator II–Lead CRC

Clinical Research Coordinator- Cardiovascular Medicine

Clinical Research Coordinator-Endocrinology, Diabetes and Metabolism

Clinical Research Assistant-Medical Oncology

Clinical Research Assistant II-Psychiatry

Clinical Research Coordinator I - RI Biobeh Fox

Research Associate- RI Clinical & Translational (Kerlin)

Clinical Research Coordinator I - RI Behav Trials Off

I want to receive the latest job alert for clinical research coordinator in ohio

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