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Trial Coordinator Jobs (NOW HIRING)

Clinical Trial Coordinator

Orlando, FL ยท On-site

$55K - $70K/yr

Role Overview The Clinical Trial Coordinator is responsible for implementing and supporting multiple clinical trial programs across SiteLabs' decentralized pharmacy network. You will act as the ...

Clinical Trial Coordinator

Miami, FL ยท On-site

$55K - $70K/yr

Role Overview The Clinical Trial Coordinator is responsible for implementing and supporting multiple clinical trial programs across SiteLabs' decentralized pharmacy network. You will act as the ...

Clinical Trial Coordinator

Miami, FL ยท On-site

$55K - $70K/yr

Role Overview The Clinical Trial Coordinator is responsible for implementing and supporting multiple clinical trial programs across SiteLabs' decentralized pharmacy network. You will act as the ...

Clinical Trial Coordinator Job Responsibilities: * Provides Trial Management Filing (TMF) system support, including document inspection, filing, and auditing. * Supports study budget negotiation and ...

Trial Logistics Coordinator

Manhattan, NY ยท On-site

$78K - $100K/yr

The Trial Logistics Coordinator will support trial preparation and execution for this boutique litigation firm, ensuring smooth coordination of logistics and administrative tasks to meet deadlines ...

Responsibilities include patient recruitment, informed consent, trial coordination, data management, and regulatory compliance. The position requires in-depth knowledge of clinical trial regulations ...

Responsibilities include patient recruitment, informed consent, trial coordination, data management, and regulatory compliance. The position requires in-depth knowledge of clinical trial regulations ...

We are immediately hiring a Pre-Trial Run Coordinator in Flint, MI for our Supply Chain Solutions division. Apply here today to speak with a Recruiter about the position and perks of joining our ...

Responsibilities include patient recruitment, informed consent, trial coordination, data management, and regulatory compliance. The position requires in-depth knowledge of clinical trial regulations ...

Responsibilities include patient recruitment, informed consent, trial coordination, data management, and regulatory compliance. The position requires in-depth knowledge of clinical trial regulations ...

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Trial Coordinator information

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$28K

$67.5K

$116K

How much do trial coordinator jobs pay per year?

As of Jul 27, 2026, the average yearly pay for trial coordinator in the United States is $67,542.00, according to ZipRecruiter salary data. Most workers in this role earn between $53,500.00 and $78,500.00 per year, depending on experience, location, and employer.

How much do clinical trial coordinators earn?

Clinical trial coordinators typically earn between $45,000 and $70,000 annually, depending on experience, location, and certifications. Entry-level positions may start lower, while experienced coordinators with specialized skills can earn higher salaries, especially in larger or research-intensive organizations.

Is CRC an entry level position?

A Clinical Research Coordinator (CRC) position is often considered entry-level, suitable for individuals with a bachelor's degree in a related field. Some roles may require prior internship or related experience, and certifications like the CCRC can enhance job prospects, but many CRC positions are accessible to those starting their clinical research careers.

What is the role of a clinical trial coordinator?

A clinical trial coordinator manages the daily operations of clinical trials, ensuring protocols are followed, data is accurately collected, and regulatory requirements are met. They coordinate between researchers, participants, and regulatory bodies, often using specialized software and maintaining detailed documentation throughout the study.

What is the difference between Trial Coordinator vs Clinical Research Associate?

AspectTrial CoordinatorClinical Research Associate
CredentialsTypically requires a bachelor's degree in health sciences or related field; certifications like CCRP are a plusRequires a bachelor's degree; often holds certifications like CCRP or RAC
Work EnvironmentManages trial logistics at study sites, interacts with staff and participantsMonitors clinical trials at multiple sites, ensuring compliance and data integrity
Employer & Industry UsageUsed mainly in hospitals, clinics, and research centersCommonly employed by pharmaceutical companies, CROs, and research institutions

While both roles support clinical trials, Trial Coordinators focus on managing site activities and participant coordination, whereas Clinical Research Associates primarily oversee trial compliance and monitor multiple sites to ensure protocol adherence.

How much does a CRC make?

A Clinical Research Coordinator (CRC) in Ohio typically earns between $50,000 and $70,000 annually, depending on experience, certifications, and the employer. Entry-level CRCs may start at lower salaries, while those with specialized skills or certifications like CCRP can earn higher wages.

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

To thrive as a Trial Coordinator, you need a strong understanding of clinical research protocols, regulatory compliance, and project management, typically supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and GCP certification is commonly required. Excellent organizational, communication, and problem-solving skills help manage multiple stakeholders and ensure trial milestones are met. These competencies are crucial to maintain data integrity, ensure regulatory adherence, and support the smooth operation of clinical trials.

What are some common challenges Trial Coordinators face when managing clinical studies, and how can they be addressed?

Trial Coordinators often manage multiple responsibilities, such as maintaining regulatory compliance, coordinating with diverse stakeholders, and ensuring accurate data collection. Common challenges include balancing tight timelines, handling protocol deviations, and facilitating clear communication between clinical staff and external partners. These can be addressed by developing strong organizational systems, proactively communicating with the study team, and staying current with regulatory requirements to anticipate and resolve issues efficiently.

What are trial coordinators?

Trial coordinators, also known as clinical trial coordinators or clinical research coordinators, are professionals who manage and oversee the day-to-day operations of clinical trials. They ensure that studies are conducted according to protocol, regulatory requirements, and ethical standards. Their responsibilities typically include recruiting and enrolling participants, collecting and managing data, maintaining study documentation, coordinating with investigators, and ensuring participant safety. Trial coordinators play a vital role in the successful execution of clinical research and the advancement of medical knowledge.
More about Trial Coordinator jobs
What cities are hiring for Trial Coordinator jobs? Cities with the most Trial Coordinator job openings:
What are the most commonly searched types of Trial jobs? The most popular types of Trial jobs are:
What states have the most Trial Coordinator jobs? States with the most job openings for Trial Coordinator jobs include:
Infographic showing various Trial Coordinator job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 80% Full Time, 16% Part Time, 1% Temporary, and 2% Contract. Highlights an 96% Physical, 2% Hybrid, and 2% Remote job distribution, with an average salary of $67,542 per year, or $32.5 per hour.

Clinical Trial Coordinator

Sitelabs

Orlando, FL โ€ข On-site

$55K - $70K/yr

Full-time

Retirement, PTO

Posted 24 days ago


Job description

About SiteLabs

SiteLabs is an early-stage, technology-forward company transforming independent pharmacies into trusted community access points for wellness screenings, clinical trials, and patient navigation. We partner with health systems, pharma sponsors, and CROs to improve patient access and health outcomes.

Our vision is to improve access to healthcare for the 100M+ people that independent pharmacies touch every year โ€” the majority of whom are based in underserved communities. We believe pharmacy staff should be empowered to practice at the top of their license, and that pharmacies should participate in programs that make a measurable impact and generate sustainable, non-prescription revenue.

Role Overview

The Clinical Trial Coordinator is responsible for implementing and supporting multiple clinical trial programs across SiteLabs' decentralized pharmacy network. You will act as the primary liaison between pharmacies, clinical partners (CROs, sponsors, GI clinics), and SiteLabs internal teams โ€” ensuring sites are equipped, compliant, and motivated to identify, refer, and retain patients.

This is a high-ownership, field-facing role suited for an organized, proactive individual with experience in clinical operations, trial recruitment, or healthcare program implementation.

Core ResponsibilitiesTrial Onboarding & Pharmacy Engagement

โ€ข Rapidly onboard and train new pharmacy sites on clinical trial workflows, protocol requirements, referral processes, and data capture.

โ€ข Serve as the primary point of contact for pharmacy staff across trials โ€” maintaining consistent communication, addressing challenges, and keeping sites engaged.

โ€ข Customize training materials and lead virtual and in-person sessions to ensure readiness and protocol adherence.

Clinical Partner Coordination

โ€ข Coordinate with trial sponsors, CROs, and downstream care partners to ensure smooth referral, scheduling, and data capture.

โ€ข Maintain protocol alignment and communication between pharmacy sites and clinical care teams.

โ€ข Support appointment scheduling and logistics, especially in time-sensitive trial environments.

Pharmacy Success & Ongoing Support

โ€ข Serve as a dedicated success partner for each pharmacy site, owning the relationship from onboarding through the full program lifecycle.

โ€ข Conduct regular check-ins to review performance, celebrate wins, address challenges, and keep sites motivated and engaged.

โ€ข Monitor site-level metrics including referral volume, lead quality, and enrollment progress โ€” proactively identifying gaps and removing barriers before they become problems.

โ€ข Share best practices across the network and act as each pharmacy's internal advocate within SiteLabs.

Performance Monitoring & Reporting

โ€ข Track pharmacy activity and recruitment performance using SiteLabs' platform and dashboards.

โ€ข Generate weekly progress reports and surface risks, gaps, or delays early.

โ€ข Partner with leadership to continuously iterate and improve implementation playbooks.

Compliance & Quality Assurance

โ€ข Ensure pharmacy execution aligns with IRB-approved materials, HIPAA standards, and GCP-compliant workflows.

โ€ข Conduct periodic site audits to validate compliance, training completion, and performance accuracy.

โ€ข Identify and escalate protocol deviations or data discrepancies promptly.

Clinical Program Support

โ€ข Support execution of non-trial clinical programs (e.g., health system screenings, patient navigation) during trial downtimes or as business needs require.

โ€ข Assist in optimizing pharmacy workflows and contributing to cross-functional clinical operations projects.

Requirements

Required

โ€ข 2 to 4 years of experience in clinical trials, patient recruitment, pharmacy operations, or decentralized clinical programs.

โ€ข Strong interpersonal and training skills with comfort leading sessions and building trusted field relationships.

โ€ข Working knowledge of IRB protocols, HIPAA, and GCP principles.

โ€ข Organized, proactive, and able to manage multiple priorities in a fast-moving environment.

โ€ข Proficient with CRM or clinical tracking systems, dashboards, and remote coordination tools.

Preferred

โ€ข Experience with independent pharmacy networks or community-based care delivery.

โ€ข Prior work with GI, oncology, metabolic, or primary care-related clinical trials.

โ€ข Experience in a startup, healthcare technology, or rapid-scale environment.

โ€ข Bilingual Spanish/English is a plus.

Benefits

โ€ข Salary: $55,000 to $70,000, based on experience

โ€ข 401(k) with company match

โ€ข 4 weeks paid time off plus 10 paid holidays

โ€ข Equity participation

โ€ข Flexible hybrid work environment with the autonomy to make a national impact