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Clinical Trials Assistant Jobs in Boca Raton, FL

Florida Cancer Specialist

Medical Assistant

Lake Worth, FL · On-site

$15.75 - $20.25/hr

S. were studied in clinical trials with FCS participation prior to approval. Through our ... RESPONSIBILITIES * Assist physicians with medical procedures in office. * Responsible for ...

Posted today

CenExel

Clinical Rater

Hollywood, FL · On-site

Each of CenExel's research sites specialize in Phase I to Phase IV clinical trials. Our Centers of ... Utilize interpersonal and clinical skills to assist in appropriate management of study participants ...

Research Centers of America

Clinical Rater

Hollywood, FL · On-site

Each of CenExel's research sites specialize in Phase I to Phase IV clinical trials. Our Centers of ... Utilize interpersonal and clinical skills to assist in appropriate management of study participants ...

CenExel

Clinical Rater

Hollywood, FL · On-site

Each of CenExel's research sites specialize in Phase I to Phase IV clinical trials. Our Centers of ... Utilize interpersonal and clinical skills to assist in appropriate management of study participants ...

CBH Health

Clinical Rater

Hollywood, FL · On-site

Each of CenExel's research sites specialize in Phase I to Phase IV clinical trials. Our Centers of ... Utilize interpersonal and clinical skills to assist in appropriate management of study participants ...

Research Centers of America

Clinical Rater

Hollywood, FL · On-site

Each of CenExel's research sites specialize in Phase I to Phase IV clinical trials. Our Centers of ... Utilize interpersonal and clinical skills to assist in appropriate management of study participants ...

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All JobsClinical Trials JobsClinical Trials Assistant JobsClinical Trials Assistant Jobs in Boca Raton, FL

Clinical Trials Assistant information

See Boca Raton, FL salary details

$10

$19

$27

How much do clinical trials assistant jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for clinical trials assistant in Boca Raton, FL is $19.20, according to ZipRecruiter salary data. Most workers in this role earn between $15.72 and $22.12 per hour, depending on experience, location, and employer.

What is a clinical trials assistant?

Clinical Trials Assistants (CTAs) are professionals who support the planning, coordination, and administration of clinical trials, which are research studies that evaluate the safety and effectiveness of medical treatments or interventions. They handle tasks such as maintaining trial documentation, assisting with regulatory submissions, scheduling meetings, and ensuring data accuracy. CTAs play a crucial role in helping clinical research teams comply with protocols and regulatory requirements, making the clinical trial process run smoothly and efficiently.

How do I become a clinical trials assistant?

To become a clinical trials assistant, candidates typically need a high school diploma or equivalent, with some roles preferring post-secondary education in health or science fields. Relevant skills include attention to detail, organization, and familiarity with clinical trial protocols; certification in Good Clinical Practice (GCP) can be beneficial. Entry-level positions often require basic computer skills and the ability to work in a team environment.

How to become a clinical trials assistant?

To become a clinical trials assistant, candidates typically need a high school diploma or equivalent, with some roles preferring post-secondary education in health or science fields. Relevant skills include attention to detail, organization, and familiarity with clinical trial protocols and documentation. Gaining experience through internships or entry-level positions in healthcare or research settings can also improve job prospects.

What are some typical challenges a clinical trials assistant faces during a study, and how can they be managed?

Clinical Trials Assistants often encounter challenges such as managing large volumes of documentation, ensuring timely data entry, and coordinating communication among multiple stakeholders. Staying organized and using established tracking systems can help manage documents efficiently. Proactive communication and regular check-ins with team members—such as study coordinators and data managers—are key to resolving issues quickly and maintaining study timelines. Embracing good time management practices and seeking mentorship from senior staff can further ease these common challenges.

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

AspectClinical Trials AssistantClinical Research Coordinator
CredentialsHigh school diploma or equivalent; some roles may require certificationBachelor’s degree in health sciences or related field; often requires certification
Work EnvironmentResearch sites, hospitals, clinics, pharmaceutical companiesResearch sites, hospitals, clinics, pharmaceutical companies
ResponsibilitiesAssist with data entry, document management, and trial logisticsOversee trial processes, patient recruitment, data collection, and compliance
Industry UsageCommonly used in clinical trial support rolesMore involved in trial management and coordination

While both roles support clinical trials, Clinical Trials Assistants focus on administrative and logistical tasks, whereas Clinical Research Coordinators handle more comprehensive trial management, patient interactions, and compliance activities.

What are the key skills and qualifications needed to thrive as a clinical trials assistant?

To thrive as a Clinical Trials Assistant, you need a solid understanding of clinical research processes, regulatory guidelines, and attention to detail, often supported by a degree in life sciences. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and Good Clinical Practice (GCP) certification is typically required. Strong organizational skills, effective communication, and the ability to multitask make candidates stand out in this role. These skills are essential for ensuring compliance, accurate documentation, and the smooth execution of clinical studies.
What are the most commonly searched types of Clinical Trials jobs in Boca Raton, FL? The most popular types of Clinical Trials jobs in Boca Raton, FL are:
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What job categories do people searching Clinical Trials Assistant jobs in Boca Raton, FL look for? The top searched job categories for Clinical Trials Assistant jobs in Boca Raton, FL are:
What cities near Boca Raton, FL are hiring for Clinical Trials Assistant jobs? Cities near Boca Raton, FL with the most Clinical Trials Assistant job openings:
Clinical Trials Assistant jobs near you
Infographic showing various Clinical Trials Assistant job openings in Boca Raton, FL as of July 2026, with employment types broken down into 2% As Needed, 78% Full Time, 14% Part Time, and 6% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $39,932 per year, or $19.2 per hour.

Psychedelic Nurse Practitioner/Physician Assistant

Segal Trials

Lauderhill, FL • On-site

$108K - $140K/yr

Other

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

Job description

🌿 Now Hiring: Psychedelic Facilitator


Segal Trials | Center of Psychedelic & Cannabis Research


Segal Trials is one of the few private research sites in the U.S. selected to conduct FDA-regulated clinical trials involving psychedelic compounds for mental health conditions. Recognized as a gold-standard research center, we are advancing the future of evidence-based psychedelic care through rigorous science, ethical practice, and compassionate participant support.


We are seeking an experienced Lead Psychedelic Facilitator to provide clinical and operational leadership across psychedelic and cannabis research trials. This role uniquely blends therapeutic presence, research rigor, and program development within a highly regulated clinical research environment.


What You’ll Do

  • Facilitate preparatory, dosing, and post-dosing integration sessions in alignment with study protocols
  • Ensure participant safety, data integrity, and adherence to GCP/GDP standards
  • Provide oversight of facilitator staffing, training, mock sessions, and ongoing performance evaluation
  • Work closely with investigators, study coordinators, raters, regulatory teams, and sponsors
  • Support program growth, sponsor engagement, recruitment efforts, and select public-facing initiatives

Who You Are

  • Psychiatric NP or PA
  • Highly experienced in working with altered states of consciousness, including preparation and integration
  • Prior psychiatric clinical research experience preferred
  • Psychedelic dosing session experience strongly desired


✨ This is a rare opportunity to help shape the future of psychedelic medicine within an elite, science-driven research organization at the forefront of clinical innovation.

👉 Apply or message us to learn more.

Apply