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Clinical Research Associate Bridge Program Jobs in Miami, FL

Myana

Senior Clinical Research Associate - Cra

Miami, FL · On-site

$80 - $100/hr

C-Clinical is seeking a Senior Clinical Research Associate to support clinical trials throughout the Miami region. The position combines remote responsibilities with routine on‑site monitoring ...

New

ICON

Senior Clinical Research Associate

Miami, FL · On-site +1

Senior Clinical Research Associate - Oncology Phase I - Miami, FL ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments ...

Icon plc

Senior Clinical Research Associate

Miami, FL · Hybrid

Senior Clinical Research Associate - Oncology Phase I - Miami, FL ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments ...

University of Miami

Research Associate 1, SOM

Miami, FL · On-site

The Research Associate 1, SOM supports research activities for the assigned division by conducting ... Attend the scheduled clinical research meetings with Clinical Research Supervisor and fellow CRCs.

University of Miami

RESEARCH ASSOCIATE 1-Myeloma

Miami, FL · On-site

$50 - $70/hr

## RESEARCH ASSOCIATE 1-MyelomaApplyremote type: On-Sitelocations: Miami, FLtime type: Full timeposted ... The candidate will assist with the integration and analysis of clinical, demographic, therapeutic ...

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Clinical Research Associate Bridge Program information

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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.

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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.

Senior Clinical Research Associate - Cra

Myana

Miami, FL • On-site

$80 - $100/hr

Other

This job post has expired today. Applications are no longer accepted.

Job description

C-Clinical is seeking a Senior Clinical Research Associate to support clinical trials throughout the Miami region. The position combines remote responsibilities with routine on‑site monitoring visits, allowing flexibility and direct engagement with investigative teams. The ideal candidate has a strong background in clinical monitoring and hands‑on experience supporting central nervous system studies, including neurology and psychiatry indications. This role involves ongoing communication with investigators, coordinators, and sponsors while supporting data quality, patient safety, and study timelines across multiple research sites.

Responsibilities
  • Coordinate with study teams to support the successful initiation and execution of clinical trials
  • Identify, evaluate, and qualify investigators and research sites within the Miami region and surrounding areas
  • Prepare and review essential documentation required for site initiation and regulatory readiness
  • Conduct on‑site monitoring visits and remote monitoring activities while maintaining detailed documentation of findings and follow‑up actions
  • Collaborate with Clinical Trial Managers and Project Managers to elevate site concerns and resolve operational challenges
  • Review study data on an ongoing basis to identify discrepancies, missing information, or protocol deviations
  • Support the full monitoring lifecycle, including pre‑study visits, site initiation visits, routine monitoring visits, and close‑out visits
  • Verify that informed consent procedures and protocol requirements are properly followed to protect research participants
  • Track and follow up on adverse events and serious adverse events while ensuring appropriate reporting procedures are followed
  • Ensure the accuracy and integrity of case report form data through a comprehensive source document review
  • Maintain compliance with study monitoring plans, standard operating procedures, and regulatory guidelines
  • Participate in investigator meetings, project team meetings, and study‑related teleconferences
  • Maintain ongoing training related to ICH GCP, study protocols, and internal procedures
  • Support regulatory documentation tracking, site performance evaluation, and study timeline adherence
Qualifications
  • Five or more years of clinical research monitoring experience as a Clinical Research Associate
  • At least three years of experience supporting studies in central nervous system indications, such as neurology or psychiatry‑related therapeutic areas
  • Minimum four years of experience working in contract‑based CRA positions, such as independent contractor, consultant, or similar arrangements
  • Experience conducting site monitoring visits and managing investigator site relationships
  • Bachelor’s degree from a four‑year university, preferably in a scientific or health‑related field (candidates with significant clinical research experience, nursing background, or relevant medical certifications may be considered in place of a traditional degree)
  • Ability to work as an independent vendor or through an established corporation or LLC with appropriate business insurance
  • Must have authorization to work in the United States
  • Must be located within the greater Miami area
  • Availability to support studies for at least one year
  • Strong communication skills in English and the ability to navigate complex clinical research discussions using medical terminology
  • Professional communication skills with the ability to collaborate effectively across study teams and research sites
  • Clinical research certifications, such as CCRA, CCRP, or similar credentials, are beneficial but not required
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