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Clinical Research Associate Bridge Program Jobs in Miami, FL

Adecco

Clinical Research Nurse

Miami, FL

$29.08/hr

... EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the ... In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other ...

Clinova Pro Services

Be Seen First

Clinical Research Coordinator

Miami Lakes, FL · On-site

$52K - $62K/yr

Associate degree or equivalent education/experience required. * Bachelor's degree in a related ... Clinical research certification such as CCRC is preferred. Preferred Experience: * Experience ...

New

Clinova Pro Services

Be Seen First

Clinical Research Coordinator

Miami Lakes, FL · On-site

$52K - $62K/yr

Associate degree or equivalent education/experience required. * Bachelor's degree in a related ... Clinical research certification such as CCRC is preferred. Preferred Experience: * Experience ...

New

Clinova Pro Services

Be Seen First

Clinical Research Coordinator

Miami Lakes, FL · On-site

$52K - $62K/yr

Associate degree or equivalent education/experience required. * Bachelor's degree in a related ... Clinical research certification such as CCRC is preferred. Preferred Experience: * Experience ...

New

The University of Miami

Research Associate 1

Miami, FL · On-site

The Research Associate 1, SOM supports research activities for the assigned division by conducting ... Support Clinical Research Coordinators in scheduling, preparing, and conducting participant study ...

University of Miami

Research Associate 1

Miami, FL · On-site

The Research Associate 1, SOM supports research activities for the assigned division by conducting ... Support Clinical Research Coordinators in scheduling, preparing, and conducting participant study ...

University of Miami

Research Associate 2

Miami, FL · On-site

The Research Associate 2, contributes to the University's research activities under the supervision ... Serve as a bridge between computational biology and wet-lab research by analyzing multi-omics ...

The University of Miami

Research Associate 2

Miami, FL · On-site

The Research Associate 2, contributes to the University's research activities under the supervision ... Serve as a bridge between computational biology and wet-lab research by analyzing multi-omics ...

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All JobsClinical Research Associate Bridge Program JobsClinical Research Associate Bridge Program Jobs in Miami, FL

Clinical Research Associate Bridge Program information

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$11

$39

$66

How much do clinical research associate bridge program jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for clinical research associate bridge program in Miami, FL is $39.33, according to ZipRecruiter salary data. Most workers in this role earn between $27.60 and $50.34 per hour, depending on experience, location, and employer.

What is a Clinical Research Associate Bridge Program?

A Clinical Research Associate (CRA) Bridge Program is a specialized training course designed to help individuals transition into the role of a CRA, especially those with related experience in healthcare, life sciences, or clinical research support. These programs typically combine classroom instruction with practical training, focusing on topics such as clinical trial monitoring, regulatory compliance, and Good Clinical Practice (GCP) guidelines. The goal is to equip participants with the necessary knowledge and skills to begin a career as a CRA, often including job placement assistance or internships. Bridge programs are ideal for those who want to move into clinical research from a related field but lack direct CRA experience.

What types of mentorship and training can I expect in a Clinical Research Associate Bridge Program?

Participants in a Clinical Research Associate (CRA) Bridge Program typically receive structured mentorship from experienced CRAs and clinical research professionals. The program often includes hands-on training in protocol review, site monitoring, regulatory compliance, and data management, combined with classroom or online learning modules. You'll work closely with cross-functional teams, such as clinical project managers and regulatory specialists, gaining exposure to industry-standard processes and tools. This supportive environment is designed to accelerate your transition into a CRA role and help you build a strong professional network within clinical research.

What are the key skills and qualifications needed to thrive as a Clinical Research Associate in a bridge program?

To thrive as a Clinical Research Associate in a bridge program, you need a foundational understanding of clinical trials, regulatory compliance, and data management, usually supported by a relevant life sciences degree. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) certification, and clinical trial management software is typically required. Strong attention to detail, effective communication, and organizational skills help you manage study protocols and collaborate with diverse teams. These competencies are crucial for ensuring clinical trial integrity, regulatory adherence, and the successful execution of research studies.

What are popular job titles related to Clinical Research Associate Bridge Program jobs in Miami, FL?

For Clinical Research Associate Bridge Program jobs in Miami, FL, the most frequently searched job titles are:

What job categories do people searching Clinical Research Associate Bridge Program jobs in Miami, FL look for?

The top searched job categories for Clinical Research Associate Bridge Program jobs in Miami, FL are:

What cities near Miami, FL are hiring for Clinical Research Associate Bridge Program jobs?

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Clinical Research Associate Bridge Program jobs near you
Infographic showing various Clinical Research Associate Bridge Program job openings in Miami, FL as of August 2026, with employment types broken down into 88% Full Time, and 12% Temporary. Highlights an 100% In-person job distribution, with an average salary of $81,816 per year, or $39.3 per hour.

Clinical Research Assistant

VENTRE MEDICAL ASSOCIATES

Fort Lauderdale, FL • On-site

Full-time

Re-posted 26 days ago

Job description

Function: The position trains with other clinical research staff and works directly with physicians to conduct clinical research trials, recruit and consent subjects, and collect and verify accuracy of data. The incumbent also assists in designing clinical trials and skill operationalizing a clinical trial in a clinical study; conducts human subject research involving multiple study sites; ensures IRB compliance; and provides communication to the Principal Investigator. 

Principal Duties & Responsibilities:

  • Assist in data management, regulatory paper works and other local administrative tasks as supervised by the clinical research coordinator
  • Coordinate research and administrative activities, ensuring all projects are completed according to project/study timelines
  • Assist in the development of project/study policies and procedures. Administer policies and procedures according to protocol, Institutional Review Board (IRB), grant/contract and study and site specifications
  • Recruit study participants and complete structured clinical assessments with participants
  • Monitor and promptly respond to participant queries
  • Collect and track study data and compile data reports
  • Submit and maintain proper study records, including submission of timely reports to Institutional Review Boards
  • Produce special and recurring reports


Other Duties as Assigned: 

The above information on this portion is designed to present the most essential duties and responsibilities necessary to achieve the positions end results. The occupant of this position is required to follow any other job-related instructions and perform any other duties as requested by Physician Director(s), Clinical Research Manager, and/or Practice Manager. It is the responsibility of each employee to assist other office staff when and where necessary. All employees have the responsibility of answering phones, maintaining files, filing, updating data, and receiving prescription refill orders, etc. Most importantly, it is each staff member’s responsibility to project and maintain a positive attitude toward all patients and fellow co- workers.  The duties listed may be changed or modified at any time.


 

  • Excellent interpersonal skills to deal effectively with clinicians, patients, administrators, auxiliary personnel, regulators, monitors and sponsors
  • Knowledge of medical terminology
  • Knowledge of good clinical practice, FDA, OHRP, HIPAA policies
  • Familiarity with the Microsoft Office Suite
  • Previous work with CRFs and EDC
  • Excellent organizational skills to independently manage work flow
  • Ability to prioritize quickly and appropriately
  • Ability to multi-task
  • Meticulous attention to detail

Education and Experience:

  • Licensed candidates must have an Associate's degree and RN or LPN licensure
  • One year of experience working in clinical research is preferred
  • Psychology background preferred

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