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Trials Manager Jobs in Florida (NOW HIRING)

Leads and executes Hematology/Oncology strategic initiatives, including CORKM grant deliverables, fertility program development, and expansion of clinical research and advanced trials. * Manages ...

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Oncology CTMS Analyst

Miami, FL · Remote

$28 - $38/hr

This fully remote opportunity is ideal for an experienced Clinical Trials Management System (CTMS) professional with a strong background supporting oncology research operations, system optimization ...

We help volunteers get involved in clinical trials which allow patients to play a more active role ... Collect, manage, and accurately enter clinical study data into electronic data capture (EDC ...

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Trials Manager information

What are the key skills and qualifications needed to thrive as a Trials Manager, and why are they important?

To thrive as a Trials Manager, you need a solid background in clinical research, project management, and regulatory compliance, typically supported by a relevant scientific degree and experience in clinical trials. Familiarity with clinical trial management systems (CTMS), Good Clinical Practice (GCP) guidelines, and often certifications like ACRP or SOCRA are highly valuable. Strong leadership, organization, and communication skills help manage multidisciplinary teams and ensure protocol adherence. These competencies are crucial for delivering safe, efficient, and compliant clinical trials that advance medical research.

What are Trials Managers?

Trials Managers are professionals responsible for overseeing and coordinating clinical trials or research studies. They manage all aspects of the trial process, including planning, organizing, and ensuring that studies are conducted in accordance with regulatory guidelines and protocols. Their role often involves liaising with sponsors, investigators, and regulatory authorities, as well as monitoring progress and reporting results. Trials Managers play a key role in ensuring that trials are completed on time, within budget, and to the required quality standards.

What are the main challenges a Trials Manager faces when coordinating multi-site clinical trials?

As a Trials Manager, one of the primary challenges when overseeing multi-site clinical trials is ensuring consistent protocol adherence and data quality across all locations. This involves frequent communication with site staff, troubleshooting logistical issues, and monitoring regulatory compliance. Additionally, balancing timelines and resources while managing diverse teams can be demanding. Successful Trials Managers proactively address these challenges through robust planning, regular site visits, and clear documentation to keep studies on track.

What is the difference between Trials Manager vs Clinical Research Coordinator?

CriteriaTrials ManagerClinical Research Coordinator
Required CredentialsBachelor's degree, experience in trial management, knowledge of regulationsBachelor's degree, clinical research experience, regulatory knowledge
Work EnvironmentOversees multiple trials, manages teams, coordinates with sponsorsHandles daily trial activities, patient interactions, data collection
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsHospitals, clinics, research institutions

The Trials Manager focuses on overseeing entire clinical trials, managing teams, and ensuring compliance across multiple studies. In contrast, the Clinical Research Coordinator handles the day-to-day activities at trial sites, working directly with patients and collecting data. Both roles require similar educational backgrounds and regulatory knowledge but differ in scope and responsibilities.

Infographic showing various Trials Manager job openings in Florida as of July 2026, with employment types broken down into 84% Full Time, 14% Part Time, and 2% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution.
Clinical Research Assistant 1-Clinical Trials Management Office

Clinical Research Assistant 1-Clinical Trials Management Office

Ohio State University

Fort Myers, FL

Part-time

Posted 25 days ago


Job description

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Job Title:Clinical Research Assistant 1-Clinical Trials Management OfficeDepartment:Medicine | Clinical Trials Management Office Earnings

This clinical research assistant role is specifically being recruited to support the Ohio State Genomic Health community health research initiative. The goals of Ohio State Genomic Health are to recruit 100,000 research participants over a 4-5-year period. Ohio State Genomic Health is a partnership with Helix, a population genomic company and the College of Medicine (COM) Center for Clinical Research Management (CCRM). As part of Ohio State Genomic Health, clinical genomic screening is also being conducted on each consented participant, with the return of positive and negative genomic screening results for three clinically actionable conditions that confer increased risk for certain types of cancer and cardiovascular disease. Please learn more about Ohio State Genomic Health here; https://wexnermedical.osu.edu/features/ohio-state-genomic-health.

Specifically, you will provide assistance in support of this program and related clinical research studies; assist with implementation and coordination of this and related studies; participate in recruitment of study participants; assist with collection, maintenance, & reporting of clinical research data in conjunction with the larger study team. Recruitment for Ohio State Genomic Health includes email invitations, phone calls with eligible and consented individuals to answer questions, and likely future in-person community recruitment events.

Minimum Education Required

High School graduate required.

Preferred Education

Bachelor's Degree preferred.

Experience Required

0 years of relevant experience required.

Preferred Experience

0-2 years of relevant experience preferred.

FUNCTION/SUBFUNCTION: Research and Scholarship/Clinical Research

CAREER BAND: Individual Contributor-Technical

CAREER LEVEL: T1

Additional Information:

This is a part-time position, 20 hours per week.

Location:Dodd Hall (0171)Position Type:RegularScheduled Hours:20Shift:First Shift

Final candidates are subject to successful completion of a background check. A drug screen or physical may be required during the post offer process.

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