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Clinical Research Program Manager Jobs in Florida

Cardiovascular Associates of America

FL · On-site

Experience managing clinical trials, leading the enrollment for multiple clinical trials, developing a research program * Strong organizational and time management skills * Clinical research ...

CVAUSA

Clinical Research Coordinator

The Villages, FL · On-site

$60 - $80/hr

... program while collaborating with clinic staff on existing and new clinical trials. As part of ... You will have the opportunity to manage your studies with a high degree of autonomy while working ...

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All JobsClinical Research Program JobsClinical Research Program Manager JobsClinical Research Program Manager Jobs in Florida

Clinical Research Program Manager information

See Florida salary details

$33.3K

$69.2K

$111.7K

How much do clinical research program manager jobs pay per year?

As of Sep 8, 2026, the average yearly pay for clinical research program manager in Florida is $69,202.00, according to ZipRecruiter salary data. Most workers in this role earn between $54,200.00 and $78,500.00 per year, depending on experience, location, and employer.

What does a clinical research program manager do?

A Clinical Research Program Manager oversees the planning, implementation, and management of clinical research studies within an organization. They coordinate research activities, ensure compliance with regulatory requirements, manage budgets, and supervise research staff. Their role is crucial in maintaining timelines, quality standards, and communication among stakeholders, including investigators, sponsors, and regulatory authorities. They also play a key part in developing study protocols and ensuring that research activities align with organizational goals.

What are the key skills and qualifications needed to thrive as a clinical research program manager?

To thrive as a Clinical Research Program Manager, you need a strong background in clinical research, project management, regulatory compliance, and often an advanced degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications such as CCRP or PMP are typically required. Excellent leadership, organizational, and communication skills set standout managers apart, enabling them to coordinate teams and stakeholders effectively. These skills and qualifications are crucial for ensuring clinical studies meet regulatory standards, stay on schedule, and achieve high-quality outcomes.

What are some typical challenges faced by clinical research program managers in coordinating multi-site studies?

Clinical Research Program Managers often encounter challenges when coordinating multi-site studies, such as ensuring consistent protocol adherence across locations, managing data collection timelines, and addressing site-specific regulatory requirements. Effective communication and strong organizational skills are essential to keep all teams aligned and to resolve issues promptly. Additionally, the role frequently involves collaborating with investigators, sponsors, and regulatory bodies to maintain study integrity and ensure compliance.

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

AspectClinical Research Program ManagerClinical Research Coordinator
CredentialsBachelor's or higher in life sciences, often with project management certificationsTypically holds a bachelor's degree in health sciences or related field
Work EnvironmentOversees multiple studies, manages teams, and coordinates with stakeholdersHandles daily study activities, patient interactions, and data collection
Employer & Industry UsagePharmaceutical companies, CROs, academic institutionsHospitals, clinics, research sites
Search & Comparison IntentFocuses on management, oversight, and program coordinationFocuses on study-specific tasks and patient management

The Clinical Research Program Manager oversees multiple research projects, manages teams, and ensures compliance across studies. In contrast, the Clinical Research Coordinator handles the day-to-day activities of individual studies, including patient interactions and data collection. Both roles require relevant credentials but differ in scope and responsibilities.

What are the most commonly searched types of Clinical Research Program jobs in Florida?

The most popular types of Clinical Research Program jobs in Florida are:

What are popular job titles related to Clinical Research Program Manager jobs in Florida?

For Clinical Research Program Manager jobs in Florida, the most frequently searched job titles are:

What job categories do people searching Clinical Research Program Manager jobs in Florida look for?

The top searched job categories for Clinical Research Program Manager jobs in Florida are:

What cities in Florida are hiring for Clinical Research Program Manager jobs?

Cities in Florida with the most Clinical Research Program Manager job openings:

Clinical Research Program Manager jobs near you
Infographic showing various Clinical Research Program Manager job openings in Florida as of September 2026, with employment types broken down into 1% As Needed, 81% Full Time, 16% Part Time, and 2% Contract. Highlights an 93% Physical, 1% Hybrid, and 6% Remote job distribution, with an average salary of $69,202 per year, or $33.3 per hour.

Sr. Lead Clinical Research Coordinator

FL • On-site

Cardiovascular Associates of America
Health Care and Social Assistance • 51 - 200 employees
Learn more about Cardiovascular Associates of Americaexternal

Full-time

Posted 23 days ago

Key responsibilities

  • Oversee all aspects of clinical trials, including patient recruitment, screening, and enrollment.

  • Handle day-to-day site management, ensuring compliance with regulatory requirements and study protocols.

  • Collect, verify, and manage clinical trial data to ensure accuracy and completeness.

Job description

Job Title: Lead Clinical Research Coordinator
Must live in Lake Nona area or willing to relocate 
 

Job Type: Full-time

About CVAUSA: Cardiovascular Associates of America (CVAUSA) is a rapidly growing leader in cardiovascular care, committed to advancing medical research and improving patient outcomes. As part of our expansion, we are quickly increasing our clinical trial operations and looking for dynamic, results-driven professionals to join our team at the MyCardiologist location in South Miami, Florida. At CVAUSA, we are focused on innovation and excellence in cardiovascular research, and we believe that the best results come from individuals who are passionate about making a difference.

MyCardiologist is hiring a Lead Clinical Research Coordinator for the South Miami location. The Lead Clinical Research Coordinator will be responsible to lead the growth and development of the research program while also working with other clinic staff on existing and new clinical trials. As part of CVAUSA’s national network, the Clinical Research Coordinator will have the opportunity to collaborate with teams across the country, making an impact on cardiovascular care both locally and nationwide.

Position Overview: As a Lead Clinical Research Coordinator at CMA, you will play a key role in managing and overseeing all aspects of clinical trials and site operations. You will have the opportunity to take ownership of your projects, driving them forward with innovation, efficiency, and excellence. This is a fantastic opportunity for an ambitious, goal-oriented individual who thrives in an independent, fast-paced environment.

Key Responsibilities:

  •   Clinical Trial Management: Oversee all aspects of clinical trials, including patient recruitment, screening, and enrollment. Ensure that protocols are followed meticulously.
  •   Site Operations: Handle day-to-day site management, ensuring that all activities comply with regulatory requirements and study protocols.
  •  Data Management: Collect, verify, and manage clinical trial data, ensuring it is accurate and complete.
  •   Communication & Reporting: Act as the primary point of contact for study sponsors, participants, and other stakeholders. Provide regular updates and progress reports.
  •  Regulatory Compliance: Ensure all documentation, including regulatory submissions and patient records, are kept up-to-date and in compliance with ethical and legal standards.
  • Problem Solving & Innovation: Identify areas for process improvement and implement solutions to drive efficiency and enhance trial operations.

What We’re Looking For:

  •   Goal-Driven & Independent: You thrive in an autonomous work environment and take full ownership of your responsibilities.
  •   Innovative & Results-Driven: You are eager to contribute to CVAUSA’s rapid growth and bring fresh, effective solutions to the table.
  •   Detail-Oriented & Highly Organized: You have the ability to manage multiple tasks and deadlines without sacrificing quality.
  •   Strong Communicator: You can effectively communicate with stakeholders at all levels, including sponsors, site staff, and participants.
  • Experience & Qualifications:
  •   Clinical experience in cardiovascular medicine in any licensed role (i.e. RN, technologist, medical assistant, etc.)
  •  Bachelor’s degree in a relevant field (e.g., life sciences, healthcare, or clinical research)
  •   Experience managing clinical trials, leading the enrollment for multiple clinical trials, developing a research program
  •   Strong organizational and time management skills
  • Clinical research certification (e.g., CCRP) is a plus
  •  Knowledge of GCP, ICH guidelines, and regulatory requirements

Why CVAUSA? At CVAUSA, we believe in the power of innovation, and we’re looking for professionals who are eager to make an impact in the field of cardiovascular research. As part of our rapidly growing organization, you’ll be at the forefront of cutting-edge clinical trials, making meaningful contributions to improving cardiovascular care. You’ll be working on site in South Miami, Florida where you will lead the growing program of cardiovascular medicine research, with opportunities to collaborate with teams nationwide. We offer competitive compensation, flexible working hours, and a supportive, dynamic environment where your contributions are valued. If you are ambitious, innovative, and ready to take your career to the next level, we want to hear from you!

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