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Clinical Study Assistant Jobs in Ohio (NOW HIRING)

Frontage Laboratories

Study Assistant

Painesville, OH · On-site

Study Assistant Location: Concord, OH (on-site) Reports To: Study Support Team Leader Company ... Our core competencies include pre-clinical, drug metabolism, pharmacokinetics/ pharmacodynamics (PK ...

AtriCure

Clinical Research Associate II

Mason, OH · On-site

The CRA II will assist with the implementation and execution of study protocols and associated study documents for clinical trials, including clinical monitoring of AtriCure studies. This also ...

AtriCure

Senior Clinical Research Associate

Mason, OH · On-site

$106K - $130K/yr

The Senior Clinical Research Associate (Sr. CRA) at AtriCure plays a vital role in the Clinical ... to study procedures and regulatory requirements. * Assist in reviewing peer interim monitoring ...

Doist

$120 - $160/hr

Collaborate with the CTAs in archiving activities. * Assist the Medical Monitor in preparing protocols, Case Report Forms, and final Clinical Study Reports. * Deliver project specific trainings.

New

Nationwide Children's Hospital

$23.75 - $31.50/hr

Summary: Manages elements of a clinical study in order to meet all protocol obligations while ... Certifications: * CNA, PCA, LPN, MA, or equivalent education or experience, required. * Clinical ...

Nationwide Children's Hospital

$23.75 - $31.50/hr

Summary: Manages elements of a clinical study in order to meet all protocol obligations while ... Certifications: * CNA, PCA, LPN, MA, or equivalent education or experience, required. * Clinical ...

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All JobsClinical Study JobsClinical Study Assistant JobsClinical Study Assistant Jobs in Ohio

Clinical Study Assistant information

See Ohio salary details

$10

$19

$27

How much do clinical study assistant jobs pay per hour?

As of Aug 20, 2026, the average hourly pay for clinical study assistant in Ohio is $19.23, according to ZipRecruiter salary data. Most workers in this role earn between $15.77 and $22.16 per hour, depending on experience, location, and employer.

What is a clinical study assistant?

Clinical Study Assistants are professionals who support the conduct of clinical trials by handling administrative tasks, maintaining study documentation, and ensuring regulatory compliance. They work closely with clinical research teams to coordinate schedules, communicate with study sites, and help manage trial materials. Their role is crucial in ensuring that clinical studies run smoothly, efficiently, and according to protocols and regulatory guidelines.

What are the key skills and qualifications needed to thrive as a clinical study assistant?

To thrive as a Clinical Study Assistant, you need strong organizational skills, attention to detail, and a background in life sciences or related fields, often supported by a bachelor's degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and regulatory documentation processes is typically required. Effective communication, teamwork, and problem-solving skills help you navigate complex study protocols and collaborate with diverse stakeholders. These abilities are crucial for ensuring the accuracy, compliance, and smooth operation of clinical research studies.

What are the main challenges a clinical study assistant might face when supporting clinical trial operations?

A Clinical Study Assistant often encounters challenges such as managing multiple tasks under tight deadlines, ensuring accurate documentation, and coordinating communication between research teams, sponsors, and regulatory bodies. Additionally, adapting to evolving study protocols and maintaining compliance with strict regulatory requirements can be demanding. Strong organizational skills, attention to detail, and proactive communication are essential for navigating these challenges successfully.

What is the difference between Clinical Study Assistant vs Clinical Research Coordinator?

AspectClinical Study AssistantClinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related fieldUsually requires a bachelor's degree, often with additional certifications in clinical research
Work EnvironmentSupports clinical trials in hospitals, research centers, or pharmaceutical companiesManages entire clinical studies, coordinating between sites, staff, and sponsors
Employer & IndustryHospitals, research institutions, pharmaceutical companiesAcademic medical centers, hospitals, research organizations
Search & Comparison IntentOften compared for entry-level roles supporting clinical trialsCompared for roles with broader responsibilities in clinical study management

The Clinical Study Assistant primarily supports clinical trial activities by assisting with data collection and documentation, while the Clinical Research Coordinator manages the overall conduct of the study, including patient recruitment and compliance. Both roles require similar educational backgrounds but differ in scope and responsibilities within the clinical research process.

What are the most commonly searched types of Clinical Study jobs in Ohio?

The most popular types of Clinical Study jobs in Ohio are:

What cities in Ohio are hiring for Clinical Study Assistant jobs?

Cities in Ohio with the most Clinical Study Assistant job openings:

Clinical Study Assistant jobs near you
Infographic showing various Clinical Study Assistant job openings in Ohio as of August 2026, with employment types broken down into 3% As Needed, 76% Full Time, 14% Part Time, and 7% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $40,005 per year, or $19.2 per hour.

Study Assistant

Frontage Laboratories

Painesville, OH • On-site

Full-time

Medical, Dental, Life, Retirement

Posted 22 days ago

Job description

Title: Study Assistant

Location: Concord, OH (on-site)

Reports To: Study Support Team Leader

Company

Frontage Laboratories Inc. is an award winning, publicly listed, full-service CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada, and China, growing significant YoY growth. Our core competencies include pre-clinical, drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials.

Position Summary:

We are seeking a highly-motivated, detail-oriented team member to support client-driven projects. The successful candidate will be an active member of the Study Support Group and will assist Study Directors on assigned studies with general client needs, drafting and issuing protocols/protocol amendments, preparing subreports, running Provantis data tables, and reviewing study data all in compliance with appropriate SOP, Protocol, and Regulatory Agency guidelines.


Roles and Responsibilities:

  • Generate Provantis data tables and create PDFs of tables for reporting
  • Draft subreports (Ophthalmology, Anatomic Pathology, Clinical Pathology, ECG), protocols, and protocol amendments.
  • Review study data, data binders, and documents generated by Study Directors/Study Support as needed.
  • Assist with drafting deviations as they arise
  • Update Toxicology Project Management system as milestone tasks are completed.
  • Review and edit grammar, styles, typefaces, and formatting based on report writing style guidelines for all generated documents.
  • Reviewing Locomotor Activity Data spreadsheets and ECGs.
  • Data entry into Provantis for various studies


Education and Requirements:

  • Associate’s or Bachelor’s Degree preferably in Life Sciences, communication, English, or similar related discipline.
    • An equivalent amount of education and/or experience may be accepted as a satisfactory substitute for the specific education.
    • Willing to train individuals with correlating background, education, or skills.
  • Proven ability to successfully work in a team environment.
  • Excellent oral and written communication skills.
  • Basic computer knowledge (e.g. Microsoft Word, Excel, Adobe Acrobat)
    • Experience with Provantis or similar LIMS software is a plus.


Salary and Benefits:

Frontage Laboratories offers a competitive compensation and generous benefits package including health and dental insurance, a 401(k) plan, health insurance, short and long-term disability insurance, life insurance etc.


Frontage Laboratories Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability.