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Clinical Study Startup Jobs in Ohio (NOW HIRING)

IQVIA

CRA 1, IQVIA Biotech

Cleveland, OH

$71K - $145K/yr

... clinical research studies by performing site monitoring and site management activities. In this ... startup activities based on study needs. Accurate and timely documentation is critical. The CRA I ...

IQVIA

CRA 1, IQVIA Biotech

Columbus, OH

$71K - $145K/yr

... clinical research studies by performing site monitoring and site management activities. In this ... startup activities based on study needs. Accurate and timely documentation is critical. The CRA I ...

IQVIA

CRA 1, IQVIA Biotech

Columbus, OH · On-site

$71K - $145K/yr

... clinical research studies by performing site monitoring and site management activities. In this ... startup activities based on study needs. Accurate and timely documentation is critical. The CRA I ...

IQVIA

CRA 1, IQVIA Biotech

Cleveland, OH

$71K - $145K/yr

... clinical research studies by performing site monitoring and site management activities. In this ... startup activities based on study needs. Accurate and timely documentation is critical. The CRA I ...

Medpace, Inc.

Supply Chain Specialist

Cincinnati, OH · Hybrid

Prepares Supply Chain startup timelines with internal colleagues and leads efforts to ensure the ... align with Clinical Trial needs. * Adjust plans & iterate Supply Chain setup when study ...

Medpace, Inc.

Supply Chain Specialist

Cincinnati, OH · On-site

Prepares Supply Chain startup timelines with internal colleagues and leads efforts to ensure the ... align with Clinical Trial needs. * Adjust plans & iterate Supply Chain setup when study ...

Medpace, Inc.

Supply Chain Manager

Cincinnati, OH · On-site

Review and approve Supply Chain startup timelines with internal colleagues and leads efforts to ... study deliverables Medpace Overview Medpace is a full-service clinical contract research ...

Medpace, Inc.

Supply Chain Manager

Cincinnati, OH · Hybrid

Review and approve Supply Chain startup timelines with internal colleagues and leads efforts to ... study deliverables Medpace Overview Medpace is a full-service clinical contract research ...

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All JobsClinical Study Startup JobsClinical Study Startup Jobs in Ohio

Clinical Study Startup information

See Ohio salary details

$27

$59

$91

How much do clinical study startup jobs pay per hour?

As of Jul 26, 2026, the average hourly pay for clinical study startup in Ohio is $59.43, according to ZipRecruiter salary data. Most workers in this role earn between $48.22 and $66.97 per hour, depending on experience, location, and employer.

What is a Clinical Study Startup job?

A Clinical Study Startup job involves managing the initial phases of a clinical trial, ensuring all regulatory, ethical, and logistical requirements are met before patient enrollment begins. Responsibilities typically include submitting regulatory documents, coordinating with ethics committees, negotiating contracts, and ensuring trial sites are fully prepared. This role requires strong knowledge of clinical research regulations, timelines, and collaboration with internal and external stakeholders. Effective study startup is crucial for minimizing delays and ensuring compliance with industry standards.

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

Success in a Clinical Study Startup role requires a strong understanding of clinical research processes, regulatory requirements, project management, and often a life sciences degree or related field. Familiarity with clinical trial management systems (CTMS), electronic trial master files (eTMF), and regulatory submission platforms is essential, along with certifications like GCP (Good Clinical Practice) being advantageous. Attention to detail, proactive problem-solving, and excellent organizational and communication skills help candidates excel. These qualifications ensure smooth study initiation, regulatory compliance, and effective cross-functional collaboration within demanding timelines.

What are the typical responsibilities of someone working in Clinical Study Startup?

Professionals in Clinical Study Startup are primarily responsible for coordinating and executing study initiation activities, including regulatory document collection, ethics submissions, site contracting, and start-up logistics. They work closely with investigators, sponsors, and cross-functional teams to ensure all regulatory and site requirements are met before the clinical trial begins. This role often involves tight deadlines and frequent communication with stakeholders both internally and externally. It's a fast-paced position that is ideal for individuals who enjoy detail-oriented work and project coordination in a collaborative environment.

What are the most commonly searched types of Clinical Study Startup jobs in Ohio? The most popular types of Clinical Study Startup jobs in Ohio are:
What are popular job titles related to Clinical Study Startup jobs in Ohio? For Clinical Study Startup jobs in Ohio, the most frequently searched job titles are:
What job categories do people searching Clinical Study Startup jobs in Ohio look for? The top searched job categories for Clinical Study Startup jobs in Ohio are:
What cities in Ohio are hiring for Clinical Study Startup jobs? Cities in Ohio with the most Clinical Study Startup job openings:
Clinical Study Startup jobs near you
Infographic showing various Clinical Study Startup job openings in Ohio as of July 2026, with employment types broken down into 2% As Needed, 77% Full Time, 15% Part Time, and 6% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $123,623 per year, or $59.4 per hour.
Clinical Study Manager

Clinical Study Manager

Cleveland Diagnostics Inc.

Cleveland, OH

$90K - $120K/yr

Full-time

Dental, Vision, Retirement, PTO

Posted yesterday

Job description

Our team is growing, and we currently have an immediate opening for a Clinical Study Manager
Title: Clinical Study Manager
Location: Onsite (Cleveland, Ohio)
Reports to: Director, Clinical Operations
Job Description: This position will oversee assigned clinical research projects, protocol development, site management, monitoring, TMF management, cross-departmental collaboration and communication, and documenting and tracking execution of projects to adhere to milestones, budgets, and targeted timelines.
Essential Duties and Responsibilities
  • Manage end-to-end lifecycle of assigned IVD clinical research projects, including startup, site management, monitoring, and closeout. Coordinate IRB submissions, laboratory shipments and incoming samples, sample receipt logging, kit creation and inventory, and ensure study deliverables are achieved on time and within budget.
  • Oversee TMF, CTMS, and database for assigned projects. Participate in development of protocols, ICFs, CRFs, and other study-related documents. Build study budgets and timelines, establish milestones, and coordinate site selection and activation. Track metrics and summarize clinical data for project updates, reports and publications.
  • Serve as the primary liaison between the sponsor, vendor, sites, and internal cross-functional teams for assigned projects.
  • Ensure project compliance with ICH-GCP guidelines, IRB requirements, FDA regulations, and any other applicable requirements.
  • Contribute to the forecasting and management of resources. Identify future potential studies to address unmet needs.
  • Support the onboarding of new technologies, progression of scientific innovation projects, and process improvement initiatives.
  • Perform all other duties as assigned.
Qualifications/Requirements
  • Bachelor's degree in a health or science field required.
  • At least 5 years of experience in clinical research, with specific experience in studies used for FDA/regulatory submission required. Direct trial management experience and prior experience working at the sponsor/CRO level required.
  • Experience in IVD or medical device clinical research strongly preferred.
  • Clinical research certification (e.g. ACRP, SOCRA) strongly preferred.
  • Knowledge of Good Clinical Practice (GCP)/ICH and medical device clinical trial guidelines, rules, and regulations. Understanding of Good Laboratory Practice (GLP), research safety, HIPAA, confidentiality, and regulatory standards amp; requirements.
  • Strong organizational skills and attention to detail. Ability to work autonomously and strong decision-making skills.
  • Excellent written and verbal communication skills.
  • Ability to travel overnight and out-of-state occasionally (20%)
Physical Requirements/ Working Conditions/Equipment Used:
  • Office reachable by elevator but should be able to climb stairs if needed
  • Light lifting may be required (up to 25 pounds)
  • Ability to work in an environment with exposure to hazardous chemicals and biohazards
  • Ability to operate a computer throughout course of day
  • General office and HVAC noise amp; fluorescent and/or LED lighting
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Cleveland Diagnostics, Inc., is developing highly efficacious, lab-friendly, affordable diagnostics tests using proprietary technology to improve cancer diagnostics. We pride ourselves in fostering a family-focused, friendly, and flexible organization that places our employee’s well-being and happiness as the primary reason for our success. Are you interested in building your career with a team of industry professionals while making a lasting impact to the lives of millions of people? Bring your talents to Cleveland Diagnostics.
Cleveland Diagnostics offers an extremely robust benefits package which includes:
  • 100% Employer-paid medical for single coverage effective on your date of hire and 50% employer-paid medical for spouse/dependent coverage
  • 100% Employer-paid Dental amp; Vision for entire family
  • No cost for employee coverage for Group Term Life, Short- amp; Long-Term Disability
  • 4% retirement contribution Employer match
  • Incentive Performance Plan amp; Stock Option Program amp; Commission (Sales Account Execs)
  • Paid Family Leave Program
  • Generous PTO plan amp; holiday program
  • Flexible work schedule amp; lucrative employee referral program
  • Salary range may vary by work state/geographical region/territory
  • Easy to get to office location with newly built-out office space
  • Free coffee, snacks and other goodies all day long
Cleveland Diagnostics is an equal opportunity employer and is committed to providing a workplace free from harassment and discrimination. We celebrate the unique differences of our employees because that is what drives curiosity, innovation, and the success of our business. EEO is the Law. Applicants can learn more about the company’s status as an equal opportunity employer by viewing the federal EEO is the Law poster on our careers page. Accommodations are available for applicants with disabilities.

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