Top 38 Clinical research associate Jobs in Cleveland Oh

Travel Clinical Research Education Trainer
The Clinical Trials Network, LLC —Cleveland, OH
- $80,000 - $100,000 a year
- Full-time
- Background check
- RN License
- 5 years
- Health insurance
- Dental insurance
Quick Apply
Clinical Research Regulatory Specialist II, Seidman Cancer Center (Hybrid)
University Hospitals —Cleveland, OH
- $56,555 - $88,442 a year
- Computer literacy
- Mid-level
- Mentoring
Research Coordinator III
Cleveland Clinic —Cleveland, OH
- $57,510.00 - $87,697.50 a year
- Full-time
- Hybrid work
- Vital signs
- Microsoft Outlook
- Hospital
- Dental insurance
- Vision insurance
8h
Research Assistant 1 (part-time 24 hours/week for approximately 18 month term)
Case Western Reserve University —Cleveland, OH
- From $17.65 an hour
- Part-time
- Office
- Driver's License
- Driving
- Disability insurance
- Health insurance
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
1d
Clinical Research Quality Assurance Specialist, Seidman Cancer Center (Hybrid)
University Hospitals —Cleveland, OH
- $60,528 - $94,661 a year
- 3 years
- Master's degree
- Bachelor's degree
Research Assistant 2 (Part Time)
Case Western Reserve University —Cleveland, OH
- $19.41 an hour
- Part-time
- Adults
- HIPAA
- Office
- Health insurance
- Tuition reimbursement
6d
Clinical Research Assistant
Great Lakes Gastroenterology —Mentor, OH
- $17 - $22 an hour
- High school diploma or GED
- Organizational skills
- 1 year
- Health savings account
- Health insurance
Quick Apply
14d
Lab Assistant, Clinical Trials Unit
University Hospitals —Cleveland, OH
- $15.00 - $22.61 an hour
- Computer literacy
- High school diploma or GED
- Ability to lift 50 pounds
2d
Research Associate – Preclinical Medical Imaging
Cleveland Clinic —Cleveland, OH
- $66,228 - $80,000 a year
- Full-time
- Surgery
- Analysis skills
- Doctor of Philosophy
- Dental insurance
- Vision insurance
Clinical Study Manager
Cleveland Diagnostics Inc. —Cleveland, OH
- $90,000 - $120,000 a year
- Urgently hiring
- 5 years
- Computer literacy
- HIPAA
- Paid holidays
- Disability insurance
Research Assistant 2
Case Western Reserve University —Cleveland, OH
- $19.41 an hour
- Full-time
- Adults
- HIPAA
- Mid-level
- Health insurance
- Tuition reimbursement
6d
Principal Investigator (Assistant, Associate or Full Staff) - Heart, Blood, and Kidney Research
Cleveland Clinic —Cleveland, OH
- $130,000 - $300,000 a year
- Full-time
- Surgery
- Senior level
- Cardiology
- Health insurance
- Dental insurance
Research Assistant - Brunswick, OH
Iterative Health —Brunswick, OH
- Full-time
- Inventory management
- High school diploma or GED
- Communication skills
Research Assistant 2 (one year term position)
Case Western Reserve University —Cleveland, OH
- From $19.41 an hour
- Full-time
- Driver's License
- 1 year
- Reliable transportation
- Disability insurance
- Health insurance
Research Nurse Coordinator - Clinical Research Unit
Cleveland Clinic —Cleveland, OH
- $30.41 - $46.38 an hour
- Part-time
- Nursing
- Patient monitoring
- RN License
- Dental insurance
- Vision insurance
Clinical Nurse Research Specialist I-Medical Oncology
University Hospitals —Cleveland, OH
- $62,629 - $97,947 a year
- Nursing
- RN License
- BLS Certification
Research Nurse - Hereditary Colon Cancer
Cleveland Clinic —Cleveland, OH
- $57,510.00 - $87,697.50 a year
- Full-time
- Hybrid work
- Nursing
- Patient monitoring
- RN License
- Dental insurance
- Work from home
Research Nurse NE - Clinical Research Unit
Cleveland Clinic —Cleveland, OH
- $27.65 - $42.17 an hour
- Full-time
- Nursing
- Patient monitoring
- RN License
- Dental insurance
- Vision insurance
Pediatric Research Nurse Coordinator
Cleveland Clinic —Cleveland, OH
- $63,250.00 - $96,467.50 a year
- Full-time
- Hybrid work
- Nursing
- Blood sampling
- Patient monitoring
- Dental insurance
- Vision insurance

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Travel Clinical Research Education Trainer

The Clinical Trials Network, LLC
Cleveland, OH

Quick Apply

Job Details

Full-time
$80,000 - $100,000 a year

Benefits

Health insurance
Dental insurance
401(k)
Paid time off
Vision insurance

Qualifications

CCRC
ICH guidelines
Clinical staff training
Bachelor's degree
Clinical training
CCRP
Productivity software
Clinical quality assurance standards
Good Clinical Practice (GCP)
Travel scheduling
FDA regulations

Full Job Description

Location: Cleveland, OH

Travel: Travel across USA, up to 50-75%

About CTNx

The Clinical Trials Network (CTNx) is dedicated to expanding access to clinical research by developing, supporting, and staffing high-performing research sites across the United States. Through operational expertise, regulatory support, compliance oversight, data management, and site development services, CTNx empowers healthcare organizations to successfully conduct clinical trials while maintaining the highest standards of quality and patient care.

As CTNx continues to grow, we are seeking a Clinical Trial Educator (CTE) to serve as a key member of our Clinical Research Operations team.

Position Summary

The Clinical Trial Educator (CTE) serves as a field-based clinical research expert responsible for developing, training, and supporting clinical research sites participating within the CTNx network.

This role acts as CTNx's on-site representative and operational trainer, ensuring investigators, coordinators, and site staff are equipped to successfully conduct clinical trials in accordance with:

Good Clinical Practice (ICH-GCP)
FDA Regulations
Sponsor Requirements
Study Protocols
CTNx Operational Standards

The Clinical Trial Educator provides hands-on support throughout site onboarding, study startup, patient recruitment, quality improvement initiatives, and remediation efforts. This individual collaborates closely with investigators, research coordinators, sponsors, CROs, and internal CTNx departments to drive operational excellence, improve enrollment performance, and ensure successful study execution across the CTNx network.

This is a full-time field-based position requiring extensive travel throughout the United States (up to 75%).

Key Responsibilities

Site Development & Training

Serve as the primary field-based trainer for CTNx-supported research sites.
Conduct on-site and virtual training for investigators, clinical research coordinators, and site personnel.
Deliver education on: Good Clinical Practice (GCP), Human Subject Protection, Protocol-specific procedures, CTNx workflows and operational standards, Source documentation requirements, Regulatory compliance expectations, Data collection and quality standards
Support onboarding of research-naïve investigators and research staff.
Develop site-specific training plans and operational improvement strategies.
Mentor site personnel to build long-term research capabilities.

Site Startup & Operational Readiness

Assess site readiness prior to study activation.
Conduct operational assessments and gap analyses.
Assist sites in implementing sponsor, protocol, and CTNx requirements.
Ensure required staffing, equipment, systems, and workflows are in place.
Participate in study startup meetings and site initiation activities.

Enrollment & Patient Recruitment Support

Partner with sites to develop patient recruitment and retention strategies.
Assist with patient identification, chart review, and prescreening initiatives.
Educate site personnel on protocol inclusion and exclusion criteria.
Support development of referral pathways with local providers and community organizations.
Monitor enrollment performance and identify opportunities for improvement.
Recommend corrective actions when recruitment goals are not being achieved.

Site Performance & Quality Improvement

Conduct routine site visits and performance assessments.
Identify operational, compliance, documentation, or enrollment challenges.
Implement corrective action plans and process improvement initiatives.
Provide remediation support for underperforming sites.
Monitor adherence to CTNx quality standards and best practices.
Escalate significant compliance or operational risks to leadership as appropriate.

Cross-Functional Collaboration

Partner closely with: Principal Investigators, Clinical Research Coordinators, CTNx Compliance & Regulatory Team, CTNx Data Operations Team, CTNx Site Engagement Team, Sponsors and CRO Partners
Participate in site strategy discussions and operational review meetings.
Support investigator meetings, study launch meetings, and sponsor interactions as needed.

Travel & Field Support

Travel to research sites to conduct: Site onboarding visits, Operational readiness assessments, Startup support visits, Training and education sessions, Enrollment support visits, Remediation and quality improvement visits
Provide both in-person and virtual support as needed.

The above list of duties is intended to describe the general nature and level of work performed by individuals assigned to this position. It is not to be construed as an exhaustive list of duties performed by the individual so classified, nor is it intended to limit or modify the right of any supervisor to assign, direct, and control the work of employees under his/her supervision.

Required Qualifications

Bachelor's Degree required.
Minimum of five (5) years of clinical research experience in private practice(s).
ACRP or SOCRA Certification (CCRC, CCRP, or equivalent).
Strong working knowledge of: ICH-GCP Guidelines, FDA Regulations, Clinical Trial Operations, Site Management Processes
Experience working directly with clinical research sites.
Demonstrated ability to independently manage travel schedules and field assignments.
Excellent presentation, facilitation, and training skills.
Strong organizational, communication, and problem-solving abilities.
Proficiency in Microsoft Office Suite and clinical research technology platforms.
Ability to travel up to 75%.

Preferred Qualifications

Active professional license or credential in one of the following: RN, NP, PA, etc
Previous experience as; Clinical Trial Educator, Clinical Research Associate (CRA), Lead Clinical Research Coordinator, Site Manager, Research Manager
Experience utilizing: CTMS Platforms, EDC Systems, CRIO eSource, Florence eRegulatory
Experience supporting community outreach and patient recruitment initiatives.

Benefits

Full time benefits available: medical, dental, vision, PTO, 401k

Why Join CTNx?

At CTNx, you will have the opportunity to directly impact the growth and success of emerging clinical research sites while helping expand patient access to innovative therapies. This role offers a unique blend of site development, education, operations, and strategic leadership, making it ideal for experienced research professionals who are passionate about mentoring others and building high-performing research programs.

Pay: $80,000.00 - $100,000.00 per year

Benefits:

401(k)
Dental insurance
Paid time off
Vision insurance

Application Question(s):

Will you now or in the future potentially require sponsorship to work in the US?

Experience:

Clinical Research: 5 years (Required)

License/Certification:

CCRC or CCRP (Preferred)

Location:

Cleveland, OH 44113 (Preferred)

Work Location: In person

Quick Apply

Refine Your Search

clinical research associate jobs in cleveland oh

Travel Clinical Research Education Trainer

Clinical Research Regulatory Specialist II, Seidman Cancer Center (Hybrid)

Research Coordinator III

Research Assistant 1 (part-time 24 hours/week for approximately 18 month term)

Clinical Research Nurse Coordinator

Clinical Research Quality Assurance Specialist, Seidman Cancer Center (Hybrid)

Research Assistant 2 (Part Time)

Clinical Research Assistant

Lab Assistant, Clinical Trials Unit

Research Associate – Preclinical Medical Imaging

Clinical Study Manager

Research Assistant 2

Principal Investigator (Assistant, Associate or Full Staff) - Heart, Blood, and Kidney Research

Research Assistant - Brunswick, OH

Research Assistant 2 (one year term position)

Research Nurse Coordinator - Clinical Research Unit

Clinical Nurse Research Specialist I-Medical Oncology

Research Nurse - Hereditary Colon Cancer

Research Nurse NE - Clinical Research Unit

Pediatric Research Nurse Coordinator

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