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Clinical Trials Associate Jobs in Florida (NOW HIRING)

Ergomed

Clinical trials, safety studies, and audits make safe and innovative pharmaceutical-led care possible. As part of Ergomed Group, you help patients benefit so they experience more of life's meaningful ...

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Clinical Trials Associate information

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$12

$29

$52

How much do clinical trials associate jobs pay per hour?

As of Aug 13, 2026, the average hourly pay for clinical trials associate in Florida is $29.88, according to ZipRecruiter salary data. Most workers in this role earn between $24.09 and $32.88 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a clinical trials associate, and why are they important?

To thrive as a Clinical Trials Associate, you need a solid understanding of clinical research protocols, regulatory compliance, and data management, typically supported by a life sciences degree. Familiarity with systems such as electronic data capture (EDC), clinical trial management systems (CTMS), and knowledge of Good Clinical Practice (GCP) guidelines or related certifications is important. Strong organizational skills, attention to detail, and effective communication help you excel in coordinating study activities and collaborating with diverse teams. These skills ensure accurate trial execution, regulatory adherence, and successful study outcomes.

What do I need to be a clinical trials associate?

To become a clinical trials associate, candidates typically need a bachelor's degree in life sciences, healthcare, or a related field. Relevant skills include knowledge of Good Clinical Practice (GCP), attention to detail, and experience with clinical trial management systems; certifications like CCRP can be advantageous.

What are some common challenges faced by clinical trials associates, and how can they be managed effectively?

Clinical Trials Associates often face challenges such as coordinating with multiple stakeholders, managing tight deadlines, and ensuring strict compliance with regulatory guidelines. Balancing administrative tasks with participant communication requires strong organizational skills and attention to detail. Staying proactive in communication, utilizing project management tools, and seeking guidance from senior team members can help manage these challenges effectively while fostering a collaborative team environment.

What is the difference between Clinical Trials Associate vs Clinical Research Coordinator?

AspectClinical Trials AssociateClinical Research Coordinator
CredentialsBachelor's degree, often in life sciences; certifications like ACRP or SOCRA are commonBachelor's degree in health sciences or related field; certifications like CCRP are advantageous
Work EnvironmentTypically works in clinical trial sites, pharmaceutical companies, or CROsWorks directly at clinical sites, hospitals, or research centers
Job FocusSupports trial setup, data entry, and regulatory complianceManages patient recruitment, scheduling, and data collection

While both roles support clinical research, Clinical Trials Associates primarily focus on trial logistics and compliance, whereas Clinical Research Coordinators handle patient interactions and site management. Both positions require similar educational backgrounds and certifications, often working in the same environments, but their daily responsibilities differ.

What is a clinical trials associate?

Clinical Trials Associates (CTAs) are professionals who support the planning, coordination, and administration of clinical research studies, often working under the supervision of Clinical Research Coordinators or Managers. Their responsibilities typically include maintaining study documentation, ensuring regulatory compliance, assisting with data collection, and communicating with study sites. CTAs play a critical role in ensuring that clinical trials run smoothly and adhere to strict protocols and guidelines. Their work helps bring new medical treatments and therapies to market safely and efficiently.
What are the most commonly searched types of Clinical Trials jobs in Florida? The most popular types of Clinical Trials jobs in Florida are:
What cities in Florida are hiring for Clinical Trials Associate jobs? Cities in Florida with the most Clinical Trials Associate job openings:
Clinical Trials Associate jobs near you
Infographic showing various Clinical Trials Associate job openings in Florida as of August 2026, with employment types broken down into 2% As Needed, 74% Full Time, 17% Part Time, and 7% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $62,152 per year, or $29.9 per hour.

Clinical Research Nurse / Paramedic (Multiple Shifts), Early Phase Clinical Trials - Daytona Beac...

Fortrea

Daytona Beach, FL • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 29 days ago

Fortrea rating

8.3

Company rating: 8.3 out of 10

Based on 11 frontline employees who took The Breakroom Quiz

26th of 73 rated research

Job description

Clinical Research Nurse / Paramedic - Early Phase Clinical Trials (Multiple Shifts Available)

Location: Daytona Beach, FL

Schedule:

  • Rotating shift and some weekends

OR

  • Night Shift:

Monday-Friday: 10hour shifts, 9:00 PM - 7:30 AM and weekends (as scheduled): 12hour shifts, 7:00 PM - 7:30 AM


Meaningful work. A chance to shape the future of medicine-while the world sleeps.

As one of the largest Clinical Research Organizations in the world, we operate four Early Phase Clinical Research Units across the UK and US. We are seeking a dedicated Rotating Shifts or Night Shift Clinical Research Nurse / Paramedic to support the execution of innovative Early Phase clinical trials, ensuring participant safety and protocol accuracy.

This role is ideal for nurses who prefer rotating shifts or night work, value schedule transparency, and thrive in a focused clinical research environment.

Why You'll Love This Role

  • Clear Shift Structure: Work primarily 10hour shifts during the week, with extended 12hour coverage on weekends as needed-providing consistency while supporting critical study operations.

  • Growth in Early Phase Research: Gain exposure to multiple therapeutic areas and firstinhuman and earlydevelopment studies, building specialized expertise in clinical research nursing.

  • PurposeDriven Impact: Maintain handson patient care while contributing directly to the development of future treatments during key overnight study periods.

  • Your Impact: You'll collaborate with leading pharmaceutical, biotechnology, and medical device companies at a critical stage of clinical development - establishing the safety, tolerability, and pharmacokinetics of new drugs. You'll maintain direct participant interaction while witnessing the development of innovative therapies firsthand.

What You'll Do

  • Deliver high-quality care to trial participants using your clinical judgment and nursing expertise.

  • Monitor participant well-being, document adverse events, and respond to emergencies.

  • Administer investigational compounds and perform study-related procedures (ECGs, telemetry, venipuncture, etc.).

  • Collect and process biological samples, maintain accurate records, and ensure compliance with protocols.

  • Other duties as assigned.

What You Bring

  • Associate's or BS degree in Nursing with current state licensure.

  • CPR/AED certification (ACLS preferred).

  • Fortrea may consider relevant and equivalent experience in lieu of educational requirements.

  • Paramedic, EMT, LVN, LPN or RN, preferred.

  • 2-3 years of related experience.

  • Phlebotomy experience.

  • A passion for learning and adaptability to a structured rotating schedule.

Join us and enjoy a role where consistency meets purpose-structured shifts that support worklife balance while you help shape the future of medicine.

Work Environment:

  • Work is performed in a laboratory and/or a clinical environment with exposure to electrical office equipment.

  • Occasional drives to site locations, occasional domestic travel.

  • Exposure to biological fluids.

  • Personal protective equipment required such as protective eyewear, garments and gloves.

Physical Requirements:

  • Ability to work in an upright and /or stationary position for 10-12 hours per day.

  • Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists to operate lab equipment.

  • Occasional crouching, stooping, with frequent bending and twisting of upper body and neck.

  • Ability to access and use a variety of computer software developed both in-house and off-the-shelf.

  • Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.

  • Regular and consistent attendance.

  • Varied hours may be required.

The important thing for us is you are comfortable working in an environment that is:

  • Fast paced: where no deviations from the study protocol are allowed, and not meeting a timeline for even few minutes will create a quality issue.

  • Changing priorities constantly asking you to prioritize and adapt on the spot.

  • Teamwork and people skills are essential for the study to run smoothly.

  • Technology based. We collect our data directly into an electronic environment.

What do you get?

Regular, full-time, or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including but not limited to:

  • Medical, Dental, Vision, Life, STD/LTD (multiple insurance carriers)

  • 401(K)

  • Paid time off (PTO)

  • Employee recognition awards

  • Multiple ERG's (employee resource groups)

Learn more about our EEO & Accommodations request here.

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