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Clinical Trials Associate Jobs in Florida (NOW HIRING)

SRA Trials

Assistant Clinical Research Coord.

Miami, FL · On-site

$20 - $22.50/hr

Assistant Clinical Research Coordinator Suncoast Research Associates is a privately owned and operated research organization established in 2018. We help volunteers get involved in clinical trials ...

ICON

Senior Clinical Research Associate

Miami, FL · On-site +1

Senior Clinical Research Associate - Oncology Phase I - Miami, FL ICON is a global healthcare ... This Sr. CRA role will support the client's Oncology clinical trials to ensure data integrity ...

Icon plc

Senior Clinical Research Associate

Miami, FL · Hybrid

Senior Clinical Research Associate - Oncology Phase I - Miami, FL ICON is a global healthcare ... This Sr. CRA role will support the client's Oncology clinical trials to ensure data integrity ...

SiteRx

Clinical Excellence Lead

Orlando, FL

You will ensure that every patient match we push to physicians is qualified to our clinical trials ... Bachelor's degree, Associate's degree or equivalent in a relevant field * You have experience ...

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Clinical Trials Associate information

See Florida salary details

$12

$29

$52

How much do clinical trials associate jobs pay per hour?

As of Aug 12, 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.

Oncology Clinical Trials Nurse, Clinical Trials, FT, 8A-4:30P

Baptist Health

Miami, FL • On-site

$40.40 - $53.73/hr

Other

Re-posted 4 days ago

Baptist Health South Florida rating

8.1

Company rating: 8.1 out of 10

Based on 99 frontline employees who took The Breakroom Quiz

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Job description

Oncology Clinical Trials Nurse

The Clinical Trials Nurse effectively conducts assigned operations of research protocols. Coordinates, evaluates and follows patient participation in clinical trials. Performs protocol specific clinical tasks including patient assessment, screening, ordering tests, collecting specimens and monitoring responses to the investigational treatment. Implement the standards for research protocols in compliance with regulatory, institutional and external agencies. Work within a Nurse-APRN-Physician ambulatory care model. Performs patient and family education / support. Collaborates with physicians in determining eligibility of patients for clinical trials. Acts as an expert consultant to investigators and others to ensure that Good Clinical Practice (GCP) standards and Standard Operating Procedures (SOP's) are followed. Provides education to staff and patients on disease pathophysiology, treatment plans and clinical trial information. Identify patient problems and recommend plan of care. The estimated pay range for this position is $40.40 - $53.73 / hour depending on experience.

Degrees: Bachelors Degree is required. Licenses & Certifications: Basic Life Support. ACRP Certified Clinical Research Associate. SOCRA Certified Clinical Research Professional. Collab Inst Training Init. ONS/ONCC Chemotherapy Immunotherapy Certificate. Registered Nurse. Additional Qualifications: BSN-Bachelors degree in Nursing. RNs hired after 2/2012 with an Associate degree will have 5 years from their date of hire to complete the BSN degree. CITI must be obtained within the first 30 days of employment. ONS chemotherapy certificate must be obtained within first 6 months of employment, Association of Clinical Research Professional (ACRP) Certification or Certified Clinical Research Professional (CCRP) Certification within 1 year of employment. Knowledge of medical terminology, nursing assessment, clinical trials and GCP concepts. Experience with computer data entry and database management. Excellent written and oral communication skills. Excellent organizational skills. Attention to details and accuracy. Ability to read, analyze, and interpret technical procedures such as protocols, informed consent documents, and regulatory documents. Ability to work independently, organize, prioritize, and follow through with results. Ability to solve practical problems and implement solutions. Effective communicator, approachable and comfortable with diverse groups of people. Aware and abide by all standards that govern good clinical practices and general nursing practice. Years of Experience: A minimum of 1 year of experience is required.

Research

Miami

Baptist Health Herbert Wertheim Cancer Institute

Full-time

Ongoing EOE, including disability/vets

What Baptist Health South Florida employees say

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Benefits

Hours and flexibility

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About Baptist Health South Florida

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Baptist Health South Florida is the largest healthcare organization in the region, with 12 hospitals, more than 27,000 employees, 4,000 physicians and 100 outpatient centers, urgent care facilities and physician practices spanning across Miami-Dade, Monroe, Broward and Palm Beach counties. Baptist Health has internationally renowned centers of excellence in cancer, cardiovascular care, orthopedics and sports medicine, and neurosciences. A not-for-profit organization supported by philanthropy and committed to its faith-based charitable mission of medical excellence, Baptist Health has been recognized by Fortune as one of the 100 Best Companies to Work For in America and by Ethisphere as one of the World's Most Ethical Companies.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Miami, FL, US

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