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Entry Level Clinical Research Associate Jobs in Florida

ICON

Clinical Research Associate II

West Palm Beach, FL · On-site +1

Clinical Research Associate - Oncology - West Palm Beach, FL ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to ...

University of Miami

RESEARCH ASSOCIATE 1-Myeloma

Miami, FL · On-site

$60 - $80/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 ...

Actalent

Clinical Research Supervisor

Orlando, FL

$95K - $120K/yr

... or Associates degree in Healthcare Administration, Research, or related field and 4 years of experience in clinical research or related field This is not a requirement to get hired but they would ...

Actalent

Clinical Research Supervisor

Orlando, FL · On-site

$95K - $120K/yr

... Associates degree in Healthcare Administration, Research, or related field and 4 years of experience in clinical research or related fieldThis is not a requirement to get hired but they would like ...

University of Miami

Research Associate 1

Miami, FL · On-site

Research Associate 1 The University of Miami/UHealth department of Neurology(Neuromuscular) has an ... regulatory specialist, clinical research coordinators or PIs This list of duties and ...

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Entry Level Clinical Research Associate information

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How much do entry level clinical research associate jobs pay per hour?

As of Sep 8, 2026, the average hourly pay for entry level clinical research associate in Florida is $22.74, according to ZipRecruiter salary data. Most workers in this role earn between $14.55 and $26.43 per hour, depending on experience, location, and employer.

What is an entry level clinical research associate?

An Entry Level Clinical Research Associate (CRA) is responsible for monitoring clinical trials to ensure compliance with regulatory requirements, ethical guidelines, and study protocols. They assist in site selection, data collection, and verifying that study procedures are properly followed. Entry-level CRAs typically work under the supervision of senior CRAs and may travel to different clinical sites. Strong attention to detail, knowledge of Good Clinical Practice (GCP) guidelines, and organizational skills are essential. This role is a starting point for a career in clinical research, with opportunities for growth into senior CRA or project management positions.

What are the typical daily responsibilities of an entry level clinical research associate?

As an Entry Level Clinical Research Associate, your day-to-day work generally involves assisting with monitoring clinical trial sites, reviewing study documentation, and ensuring adherence to protocol and regulatory requirements. You may support more senior team members in conducting on-site or remote visits, tracking patient recruitment, and managing data collection. Additionally, you’ll communicate regularly with site staff and other stakeholders to resolve issues and ensure data quality. This hands-on experience is essential for building expertise in clinical research processes and advancing toward more senior CRA roles.

What are the key skills and qualifications needed to thrive as an entry level clinical research associate?

To thrive as an Entry Level Clinical Research Associate, you typically need a bachelor's degree in life sciences or a related field, a solid understanding of clinical trial protocols, and attention to detail. Familiarity with Good Clinical Practice (GCP) guidelines, electronic data capture (EDC) systems, and regulatory documentation is often required. Strong communication, organization, and problem-solving abilities help you effectively collaborate with study sites and team members. These skills are critical to ensure the accuracy, compliance, and successful progression of clinical studies.

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

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

What are popular job titles related to Entry Level Clinical Research Associate jobs in Florida?

For Entry Level Clinical Research Associate jobs in Florida, the most frequently searched job titles are:

What job categories do people searching Entry Level Clinical Research Associate jobs in Florida look for?

The top searched job categories for Entry Level Clinical Research Associate jobs in Florida are:

What cities in Florida are hiring for Entry Level Clinical Research Associate jobs?

Cities in Florida with the most Entry Level Clinical Research Associate job openings:

Entry Level Clinical Research Associate jobs near you
Infographic showing various Entry Level Clinical Research Associate job openings in Florida as of September 2026, with employment types broken down into 2% As Needed, 77% Full Time, 15% Part Time, and 6% Contract. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution, with an average salary of $47,300 per year, or $22.7 per hour.

Clinical Research Associate II

Icon plc

Fort Lauderdale, FL

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 29 days ago

Job description

Clinical Research Associate - Oncology - West Palm Beach, FL

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


What You Will Be Doing:

  • Serve as the primary point of contact between investigational sites and the sponsor

  • Conduct all types of site visits, including selection, initiation, routine monitoring, and close-out

  • Ensure site compliance with ICH-GCP, SOPs, and regulations

  • Maintain up-to-date documentation in CTMS and eTMF systems

  • Support and track site staff training and maintain compliance records

  • Monitor patient safety, ensuring timely and accurate AE/SAE/PQC reporting

  • Support subject recruitment and retention efforts at the site level

  • Oversee drug accountability and ensure proper storage, return, or destruction

  • Resolve data queries and drive timely, high-quality data entry

  • Document site progress and escalate risks or issues to the clinical team

  • Assist in tracking site budgets and ensuring timely site payments (as applicable)

  • Collaborate with cross-functional partners including CTAs, LTMs, and CTMs

You are:

  • A graduate with a Bachelor's degree in Life Sciences or equivalent, or a qualified RN

  • Eligible to work in United States without visa sponsorship

  • A clinical research professional with 2+ years of on-site monitoring experience in the pharmaceutical or CRO industry

  • Experienced monitoring Oncology (I.e. Prostate Cancer, and Lung Cancer) and/or Hematology Oncology clinical studies

  • Proficient in ICH-GCP, local regulatory requirements, and clinical systems like CTMS and eTMF

  • A clear communicator, problem-solver, and collaborative team player

  • Willing and able to travel up to 50% for on-site monitoring visits across southeast region; preference given to candidates residing in West Palm Beach, FL near major HUB airports to support efficient regional travel


Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a requesthere.

Are you a current ICON Employee? Please click here to apply

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