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Study Monitor Jobs in Florida (NOW HIRING)

UAB

CLINICAL RESEARCH COORDINATOR II

Tampa, FL · On-site

$50K - $81K/yr

Prepares for study monitoring visits. * Ensures that documents such as eligibility forms and informed consent are appropriately gathered and maintained, and IRB-, Good Clinical Practice-, and HIPAA ...

Alcanza

Psychometric Rater

Lakeland, FL · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Meet with Sponsors, Study Monitors, and Medical Monitors as needed to address questions regarding ratings. * Working diligently to maintain consistency in the performance of ratings. Reviewing ...

Alcanza

Psychometric Rater

Deland, FL · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Meet with Sponsors, Study Monitors, and Medical Monitors as needed to address questions regarding ratings. * Working diligently to maintain consistency in the performance of ratings. Reviewing ...

RadNet

Clinical Research Manager

Fort Myers, FL · On-site

$62K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

Monitor study timelines, enrollment targets, and imaging turnaround times * Train technologists and site staff on study-specific imaging protocols and workflows * Develop SOPs and reference materials ...

RadNet

Clinical Research Manager

Fort Myers, FL · On-site

$62K - $83K/yr

Monitor study timelines, enrollment targets, and imaging turnaround times * Train technologists and site staff on study-specific imaging protocols and workflows * Develop SOPs and reference materials ...

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Study Monitor information

What is a study monitor?

A Study Monitor, also known as a Clinical Research Associate (CRA), is responsible for overseeing clinical trials to ensure they comply with regulatory guidelines, study protocols, and ethical standards. They monitor site activities, review data accuracy, and ensure participant safety. Study Monitors work closely with investigators, site staff, and sponsors to ensure the integrity of trial results and adherence to Good Clinical Practice (GCP) guidelines.

What are the key skills and qualifications needed to thrive as a study monitor?

To thrive as a Study Monitor, you need a strong understanding of clinical trial protocols, regulatory guidelines (such as GCP), and data integrity principles, typically supported by a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and certifications like ACRP or SOCRA are commonly expected. Excellent attention to detail, strong organizational skills, and effective communication are crucial soft skills. These competencies ensure high-quality study oversight, compliance with regulations, and smooth collaboration among clinical research teams.

What are some common challenges study monitors face during clinical trials?

Study Monitors often encounter challenges such as ensuring consistent protocol adherence across multiple sites, managing discrepancies in data, and navigating tight timelines for site visits and reporting. They must adapt quickly to evolving regulatory requirements and effectively communicate any issues or deviations to investigators and sponsors. Being proactive in identifying potential risks and fostering strong relationships with site staff can help minimize these challenges. As a result, successful Study Monitors need to be resourceful, detail-oriented, and skilled at balancing regulatory compliance with practical problem-solving in dynamic trial environments.

How do you become a study monitor?

To become a study monitor, candidates typically need to be students with good academic standing and demonstrate responsibility. The process often involves applying through the school or organization, sometimes including an interview or recommendation, and may require training on supervision and safety protocols.

What are popular job titles related to Study Monitor jobs in Florida?

For Study Monitor jobs in Florida, the most frequently searched job titles are:

What job categories do people searching Study Monitor jobs in Florida look for?

The top searched job categories for Study Monitor jobs in Florida are:

Study Monitor jobs near you
Infographic showing various Study Monitor job openings in Florida as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution.

Cardiologist - Principal Investigator Opportunity (Clinical Research)

DM FAMILY CARE LLC

Miami, FL • On-site

Part-time

Re-posted 21 days ago

Job description

DM Family Care in Miami, FL, is expanding into the clinical research field. Our mission is to advance innovative medical therapies by conducting high-quality clinical trials in a professional, patient-centered environment. Research activities will take place at DM Family Care’s facility, where we combine the trust of a community practice with the rigor of clinical research.

We are seeking a Florida-licensed cardiologist to join our team as a Principal Investigator in our clinical research program. The physician will provide medical oversight, evaluate study participants, and ensure regulatory compliance across multiple therapeutic areas. This hybrid position allows for flexibility, with some tasks performed remotely, but requires on-site participation at our Miami facility.

Key Responsibilities

  • Conduct medical assessments and physical exams of study participants

  • Provide expert input for cardiovascular, metabolic, and hypertension studies.

  • Serve as Principal Investigator (PI) on upcoming Phase II–III clinical trials.

  • Review and sign study-related documents, labs, and safety reports

  • Provide ongoing medical oversight throughout clinical trials

  • Ensure compliance with FDA, GCP, IRB, and study sponsor requirements

  • Collaborate with research coordinators, nurses, and study monitors

  • Maintain accurate and timely study documentation

Qualifications

  • Required:

    • Board Certified / Board Eligible Cardiologist.

    • Active Florida Medical License (required).

    • Prior research experience preferred but not required

    • GCP training required.

    • Strong clinical judgment and collaborative communication style.

    • Bilingual (English/Spanish) preferred but not required.

  • Preferred (not mandatory):

    • Prior experience in clinical research or trials

Work Environment & Schedule

  • Hybrid role: combination of remote responsibilities and required on-site participation at our Miami location

  • Flexible schedule, tailored to study demands (ideal for physicians maintaining their own practice).

Compensation

  • Compensation is structured as a revenue-sharing model, with the physician receiving 20% of physician-related study revenue for awarded trials. Details will be discussed during the interview process.
  • Opportunity to grow into a long-term research leadership role as new trials launch.

Company Description

DM Family Care, based in Miami, FL, is a trusted primary care provider now expanding into clinical research under Novelty Clinical Research. Our mission is to combine compassionate, community-based medical care with innovative research that advances future therapies. We value teamwork, growth, and excellence, offering our staff a supportive environment where they can make a meaningful impact in both patient care and medical advancement.