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Clinical Operations Associate Jobs in Columbus, OH

ChenMed

Associate Chief Clinical Officer

Columbus, OH · On-site

$238K - $341K/yr

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 ...

Jazz Pharmaceutical

Global Study Leader

London, OH

Acts as an SME for Clinical Operations related sections. * Lead the development and review of trial ... Mentor and coach Global Study Managers (GSMs) Clinical Research Associates (CRAs), and Global Study ...

New

Outcomes

Clinical Program Manager - Pharmacist

Dublin, OH · On-site

$114K - $136K/yr

Collaborate with Clinical Operations, Product, Quality, and technology to develop new covered ... Flex PTO for Exempt Associates & up to 15 PTO days in first year of employment for non-exempt ...

New

Centerwell

Home Health Clinical Manager

Delaware, OH · On-site

Oversee clinical operations for the location, including patient care delivery, staff management ... Associate benefits are designed to encourage personal wellness and smart healthcare decisions for ...

ChenMed

Associate Clinical Manager

Columbus, OH · On-site

$238K - $341K/yr

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 ...

ChenMed

Center Clinical Director, Associate

Stoutsville, OH · On-site

$238K - $341K/yr

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 ...

ChenMed

Center Clinical Director, Associate

Grove City, OH · On-site

$238K - $341K/yr

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 ...

ChenMed

Center Clinical Director, Associate

Columbus, OH · On-site

$238K - $341K/yr

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 ...

ChenMed

Center Clinical Director, Associate

Brice, OH · On-site

$238K - $341K/yr

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 ...

ChenMed

Center Clinical Director, Associate

Hilliard, OH · On-site

$238K - $341K/yr

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 ...

ChenMed

Center Clinical Director, Associate

Columbus, OH · On-site

$238K - $341K/yr

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 ...

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Clinical Operations Associate information

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How much do clinical operations associate jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for clinical operations associate in Columbus, OH is $24.71, according to ZipRecruiter salary data. Most workers in this role earn between $16.73 and $28.51 per hour, depending on experience, location, and employer.

What is a clinical operations associate?

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 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 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 most commonly searched types of Clinical Operations jobs in Columbus, OH?

The most popular types of Clinical Operations jobs in Columbus, OH are:

What are popular job titles related to Clinical Operations Associate jobs in Columbus, OH?

For Clinical Operations Associate jobs in Columbus, OH, the most frequently searched job titles are:

What job categories do people searching Clinical Operations Associate jobs in Columbus, OH look for?

The top searched job categories for Clinical Operations Associate jobs in Columbus, OH are:

What cities near Columbus, OH are hiring for Clinical Operations Associate jobs?

Cities near Columbus, OH with the most Clinical Operations Associate job openings:

Clinical Operations Associate jobs near you
Infographic showing various Clinical Operations Associate job openings in Columbus, OH as of August 2026, with employment types broken down into 100% Full Time. Highlights an 50% In-person, and 50% Hybrid job distribution, with an average salary of $51,388 per year, or $24.7 per hour.

Clinical Research Associate (Sample Management)

Astrix Inc

Columbus, OH • On-site

$27 - $29/hr

Full-time

Posted 19 days ago

Job description

Pay Rate Low: 26 | Pay Rate High: 29
Research Associate I
Location: Columbus, OH - 100% Onsite
Pay Rate: $27-$29/hour
Contract: 1 year contract (possibility of extension and/or conversion to permanent)
Start Date: ASAP - ideally by the end of August
About the Role
Our client is seeking a motivated Research Associate to support clinical research operations and sample management within a GCP/GLP environment. This role will work closely with internal teams, clinical and laboratory sites, CROs, vendors, and external collaborators to support sample logistics, documentation, database management, and day-to-day clinical research activities.
The Research Associate will help support domestic and international biopsy surgical and laboratory sites, coordinate sample shipments and tracking, maintain training documentation, and assist with specialty laboratory vendor management. This position will collaborate closely with the Laboratory Operations and Sample Management teams across clinical and pre-clinical studies.
Key Responsibilities
  • Support translational biology programs involving Gene Therapy, RNA, siRNA, and Gene Editing.
  • Coordinate clinical sample logistics, including tracking, reconciliation, and paper/electronic recordkeeping.
  • Manage sample tracking and consent information within centralized databases.
  • Assist with the development and implementation of sample management processes and databases.
  • Coordinate and track clinical trial supplies.
  • Track and reconcile incoming sample shipments across clinical and pre-clinical studies.
  • Maintain compliance with GCP/GLP guidelines, FDA regulations, and ICH guidelines.
  • Develop and maintain training manuals, resources, and documentation for clinical trial biopsy sites.
  • Collaborate with Clinical Operations, Data Management, Biostatistics, CROs, vendors, and external collaborators.
  • Support data transfers and analysis needs.
  • Build and maintain effective relationships with key internal and external stakeholders.
  • Assist laboratory teams with writing and reviewing SOPs, reports, and publications related to clinical analyses.
  • Support departmental metrics and reporting as needed.
  • Help identify and resolve complex sample management and operational issues.

Qualifications
  • Bachelor's degree in Biology, Biochemistry, or a related scientific field.
  • 2+ years of hands-on clinical sample management or clinical research operations experience within a biotech or healthcare environment.
  • Experience working in a GCP/GLP-regulated environment.
  • Strong understanding of laboratory SOPs and quality requirements for sample handling.
  • Ability to handle confidential information with discretion and sound judgment.
  • Strong organizational skills with the ability to manage multiple priorities in a fast-paced environment.
  • Excellent written and verbal communication skills.
  • Ability to communicate complex technical information clearly to both internal teams and external stakeholders.
  • Strong teamwork and collaboration skills.
  • Demonstrated problem-solving abilities and attention to detail.
  • Experience developing or maintaining training materials, procedures, and documentation is preferred.
  • Ability and willingness to work 100% onsite in Columbus, OH.
  • Must be available to start ASAP, ideally by the end of August.
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