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Clinical Operations Associate Jobs in Ohio (NOW HIRING)

The remainder of their time is allocated to leadership responsibilities, including PCP performance, engagement, and building a strong clinical-operations synergy and culture. The allocation of time ...

The remainder of their time is allocated to leadership responsibilities, including PCP performance, engagement, and building a strong clinical-operations synergy and culture. The allocation of time ...

Chief Clinical Officer

Maple Heights, OH · On-site

$238K - $341K/yr

The Associate Center Clinical Director will directly supervise and train primary care providers ... Partnering with Center Operations Director/Market General Manager to drive continued improvement of ...

The Associate Center Clinical Director will directly supervise and train primary care providers ... Partnering with Center Operations Director/Market General Manager to drive continued improvement of ...

... operations in the assigned market for Employer Solutions. This may include (but not limited to) onsite clinics, WorkHealth, Associate Health, substance testing, fitness and wellness and business ...

Chief Clinical Officer

Cincinnati, OH · On-site

$257K - $368K/yr

POSITION SUMMARY The Associate Market Clinical Director will directly supervise, performance manage ... Ensures successful clinical operations and meeting/exceeding plan market earnings. * Manages ...

The Associate Center Clinical Director will directly supervise and train primary care providers ... Partnering with Center Operations Director/Market General Manager to drive continued improvement of ...

... operational leadership, and other key stakeholders to maximize efficient and effective use of ... Associate's Degree (Required) Additional * degree in Nursing or other healthcare related field.

... operational leadership, and other key stakeholders to maximize efficient and effective use of ... Associate's Degree (Required) Additional * degree in Nursing or other healthcare related field.

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Clinical Operations Associate information

See Ohio salary details

$10

$24

$50

How much do clinical operations associate jobs pay per hour?

As of Jul 20, 2026, the average hourly pay for clinical operations associate in Ohio is $24.95, according to ZipRecruiter salary data. Most workers in this role earn between $16.92 and $28.80 per hour, depending on experience, location, and employer.

What is a Clinical Operations Associate job?

A Clinical Operations Associate supports the planning, execution, and management of clinical trials to ensure compliance with regulatory guidelines and company protocols. They assist in coordinating trial logistics, managing documentation, and communicating with study sites and stakeholders. Their role helps ensure studies run efficiently, meet regulatory requirements, and generate reliable data for drug development and approvals.

What are the key skills and qualifications needed to thrive in the Clinical Operations Associate position, and why are they important?

To thrive as a Clinical Operations Associate, you need a solid background in clinical research processes, project management, and regulatory compliance, often supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and Good Clinical Practice (GCP) certification is highly valued. Attention to detail, strong organizational skills, and effective communication are important soft skills that help manage complex studies and collaborate with cross-functional teams. These abilities are crucial for ensuring that clinical trials run smoothly, meet regulatory standards, and maintain participant safety.

What are the typical responsibilities and team dynamics for a Clinical Operations Associate?

As a Clinical Operations Associate, your typical responsibilities include coordinating study activities, maintaining trial documentation, supporting regulatory submissions, and ensuring adherence to protocols and timelines. You will often work as part of a multi-disciplinary team that includes clinical research coordinators, data managers, and study monitors, frequently communicating with internal and external stakeholders to keep the study on track. Collaboration and adaptability are key, as priorities can shift based on site needs or regulatory updates. This role offers valuable exposure to the operations side of clinical research and can serve as a springboard to more senior roles such as Clinical Project Manager or Clinical Research Associate.

What are the most commonly searched types of Clinical Operations jobs in Ohio? The most popular types of Clinical Operations jobs in Ohio are:
What are popular job titles related to Clinical Operations Associate jobs in Ohio? For Clinical Operations Associate jobs in Ohio, the most frequently searched job titles are:
What cities in Ohio are hiring for Clinical Operations Associate jobs? Cities in Ohio with the most Clinical Operations Associate job openings:
Infographic showing various Clinical Operations Associate job openings in Ohio as of July 2026, with employment types broken down into 1% As Needed, 68% Full Time, 29% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $51,897 per year, or $25 per hour.
Clinical Sample Specialist - Biospecimen Operations

Clinical Sample Specialist - Biospecimen Operations

labconnect

Cleveland, OH • On-site

Other

Re-posted 16 days ago


Job description

Job Summary

The Clinical Sample Specialist is responsible for sample management activities for samples arriving at LabConnect Cleveland facility. The Clinical Sample Specialist will perform tasks in support of receiving specimens for storage, onsite processing, or shipments to partner laboratories or other facilities. The role will also communicate with other departments such as Client Services (CS), Sample Tracking Solutions (STS), and Clinical Trial Materials (CTM) to ensure the timely and accurate handling of samples.

Essential Duties and Responsibilities

  • Ensure tasks and data are completed with accuracy and attention to detail.

  • Sample shipment receipt, inbound tracking documentation and breakdown of kits received

  • Specimen transport to different areas within the facility

  • Order requisition registration and accessioning

  • Specimen labeling

  • Assist with quality control (QC) of specimens for courier pick-ups, scheduled shipments, ad hoc shipments, specimen destructions and same day shipping packages

  • Identification of sample discrepancies and ability to follow appropriate escalation paths

  • Assist with QC checks on specimens from storage for shipmentsand destruction

  • Handling, recycling and disposal of dry ice

  • Storage freezer and refrigerator maintenance

  • Disposal of shipping materials

  • Restock supplies

  • Scan requisitions

  • Reply to emails in a timely manner

  • Completion of daily checklists

  • Attend classes/meetings, to include dangerous goods training

  • Completion of 6 hours of continuing education per year

  • Knowledge of Good Documentation Practice (GDP)and universal safety precautions

  • Other duties as required by management

Education and Experience

High school diploma or general education degree (GED) required.BA/BS, in laboratory science, health science, or business; or an associate’s degree with at least 2 years of clinical research, clinical lab, or other relevant experience preferred. 

Skills and Ability

  • Knowledge of Microsoft applications, including Word and Excel. 

  • Ability to work in various computer systems such as Laboratory Information Management Systems. 

  • Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals. 

  • Ability to write routine reports and correspondence.

  • Exceptional communication, organizational, and interpersonal skills.

  • Ability to speak effectively before groups.

  • Capable of executing instructions provided in oral, written, or diagram form.

  • Able to troubleshoot issues related to specimen management.

  •  

Supervisory Responsibilities: None

Physical Demands: 

While performing the duties of this job, the occupant is regularly required to:

Sit 50% of the time.

  • Stand 50% of the time.

  • Walk and/or reach with hands and arms 50% of the time.

  • Read text of various sizes.

  • Communicate with others and hear.

  • Lift, pull and/or push up to 50 pounds.

  • Work in an environment with moderate noise levels. 

Travel Requirements: None