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Clinical Trial Program Manager Jobs in Florida (NOW HIRING)

Clinical Trial Coordinator

Miami, FL ยท On-site

$55K - $70K/yr

Clinical Program Support * Support execution of non-trial clinical programs (e.g., health system ... Proficient with CRM or clinical tracking systems, dashboards, and remote coordination tools.

Clinical Trial Coordinator

Orlando, FL ยท On-site

$55K - $70K/yr

Clinical Program Support * Support execution of non-trial clinical programs (e.g., health system ... Proficient with CRM or clinical tracking systems, dashboards, and remote coordination tools.

Clinical Trial Coordinator

Miami, FL ยท On-site

$55K - $70K/yr

Clinical Program Support โ€ข Support execution of non-trial clinical programs (e.g., health system ... manage multiple priorities in a fast-moving environment. โ€ข Proficient with CRM or clinical ...

Clinical Trial Liaison ICON is a global healthcare intelligence and clinical research organisation ... Clinical Investigator Management * Accountable for the full spectrum of investigator engagement ...

Clinical Trial Liaison ICON is a global healthcare intelligence and clinical research organisation ... Clinical Investigator Management * Accountable for the full spectrum of investigator engagement ...

Clinical Trial Liaison ICON is a global healthcare intelligence and clinical research organisation ... Clinical Investigator Management * Accountable for the full spectrum of investigator engagement ...

Clinical Trial Liaison ICON is a global healthcare intelligence and clinical research organisation ... Clinical Investigator Management * Accountable for the full spectrum of investigator engagement ...

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Clinical Trial Assistant

Miami, FL ยท On-site

$180 - $240/day

Clinical Trial Visit Flow Manager Internal Title: Visit Expediter / Agilizador de Visitas Position Summary The Clinical Trial Visit Flow Manager is responsible for ensuring that every clinical-trial ...

New

Ensures compliance with the Clinical Trial Management System (CTMS), Electronic Trial Master (eTMF ... Wellness Incentive Program * Free Onsite Medical Clinics * Free Onsite Lunch * Tuition ...

Ensures compliance with the Clinical Trial Management System (CTMS), Electronic Trial Master (eTMF ... Wellness Incentive Program * Free Onsite Medical Clinics * Free Onsite Lunch * Tuition ...

... program during a 15-week contract assignment. This role is responsible for overseeing the ... The ideal candidate has strong leadership skills, experience managing clinical trial operations ...

Study Manager

Miami, FL ยท On-site

$85K - $95K/yr

Evolution Research Group (ERG) is dedicated to delivering high-quality Phase I-IV clinical trial ... The Study Manager (SM) is responsible for the management of all aspects of Clinical Trial Team ...

Responsible for independently leading the clinical trial study team and managing global clinical ... Implement solid strategy, scope, process, and programs related to clinical trials including leading ...

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Clinical Trial Program Manager information

See Florida salary details

$21

$49

$80

How much do clinical trial program manager jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for clinical trial program manager in Florida is $50.00, according to ZipRecruiter salary data. Most workers in this role earn between $37.45 and $59.52 per hour, depending on experience, location, and employer.

What does a clinical trial program manager do?

A Clinical Trial Program Manager oversees the planning, execution, and completion of clinical trials within an organization. They coordinate cross-functional teams, manage timelines and budgets, ensure compliance with regulatory guidelines, and maintain the quality and integrity of clinical data. Their role is essential for the successful development of new medical treatments, as they bridge communication between stakeholders, monitor progress, and address any issues that arise during trials.

What are some common challenges faced by clinical trial program managers, and how can they be addressed?

Clinical Trial Program Managers often encounter challenges such as managing complex timelines, coordinating multiple stakeholders, and ensuring regulatory compliance across different study sites. These challenges can be addressed by implementing robust project management tools, maintaining clear and consistent communication with cross-functional teams, and staying updated on regulatory requirements. Developing strong organizational skills and fostering collaborative relationships with investigators, sponsors, and regulatory bodies are also key to overcoming obstacles in this role.

What are the key skills and qualifications needed to thrive as a clinical trial program manager, and why are they important?

To thrive as a Clinical Trial Program Manager, you need strong project management skills, a background in life sciences or healthcare, and experience with clinical research regulations such as GCP, often supported by a relevant degree and certifications like PMP or ACRP. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and regulatory submission tools is typically required. Exceptional leadership, communication, and problem-solving abilities help you coordinate teams and manage complex stakeholder relationships. These skills ensure that clinical trials are conducted efficiently, compliantly, and successfully, leading to reliable study outcomes and regulatory approval.
What are popular job titles related to Clinical Trial Program Manager jobs in Florida? For Clinical Trial Program Manager jobs in Florida, the most frequently searched job titles are:
What cities in Florida are hiring for Clinical Trial Program Manager jobs? Cities in Florida with the most Clinical Trial Program Manager job openings:

Clinical Trial Coordinator

Sitelabs

Miami, FL โ€ข On-site

$55K - $70K/yr

Full-time

Retirement, PTO

Re-posted 6 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 — 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 — 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

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

• Serve as the primary point of contact for pharmacy staff across trials — maintaining consistent communication, addressing challenges, and keeping sites engaged.

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

Clinical Partner Coordination

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

• Maintain protocol alignment and communication between pharmacy sites and clinical care teams.

• Support appointment scheduling and logistics, especially in time-sensitive trial environments.

Pharmacy Success & Ongoing Support

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

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

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

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

Performance Monitoring & Reporting

• Track pharmacy activity and recruitment performance using SiteLabs' platform and dashboards.

• Generate weekly progress reports and surface risks, gaps, or delays early.

• Partner with leadership to continuously iterate and improve implementation playbooks.

Compliance & Quality Assurance

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

• Conduct periodic site audits to validate compliance, training completion, and performance accuracy.

• Identify and escalate protocol deviations or data discrepancies promptly.

Clinical Program Support

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

• Assist in optimizing pharmacy workflows and contributing to cross-functional clinical operations projects.

Requirements

Required

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

• Strong interpersonal and training skills with comfort leading sessions and building trusted field relationships.

• Working knowledge of IRB protocols, HIPAA, and GCP principles.

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

• Proficient with CRM or clinical tracking systems, dashboards, and remote coordination tools.

Preferred

• Experience with independent pharmacy networks or community-based care delivery.

• Prior work with GI, oncology, metabolic, or primary care-related clinical trials.

• Experience in a startup, healthcare technology, or rapid-scale environment.

• Bilingual Spanish/English is a plus.

Benefits

• Salary: $55,000 to $70,000, based on experience

• 401(k) with company match

• 4 weeks paid time off plus 10 paid holidays

• Equity participation

• Flexible hybrid work environment with the autonomy to make a national impact