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Clinical Trial Jobs in Boca Raton, FL (NOW HIRING)

Headlands Research

Clinical Research Coordinator

Lake Worth, FL · On-site

$21.50 - $28.75/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing ...

Headlands Research

Clinical Research Coordinator

Lake Worth, FL · On-site

$21.50 - $28.75/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing ...

Jobtailor

Director, Clinical Research

Fort Lauderdale, FL · On-site

$140 - $200/hr

Ensures all clinical trial projects (internal and external), including project management, tracking and reporting trial progress and monitoring test item expiration dates in relation to project ...

Flourish Research

Clinical Research Coordinator

Boca Raton, FL

$23 - $30.50/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Flourish Research is one of the industry's most progressive and diversified clinical trial organizations, with strong capabilities across cardiology, metabolic disorders, renal, oncology, CNS ...

Flourish Research

Clinical Research Coordinator

Boca Raton, FL · On-site

$23 - $30.50/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Flourish Research is one of the industry's most progressive and diversified clinical trial organizations, with strong capabilities across cardiology, metabolic disorders, renal, oncology, CNS ...

Flourish Research

Clinical Research Coordinator

Boca Raton, FL

$23 - $30.50/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Flourish Research is one of the industry's most progressive and diversified clinical trial organizations, with strong capabilities across cardiology, metabolic disorders, renal, oncology, CNS ...

Flourish Research

Clinical Research Coordinator

Boca Raton, FL · On-site

$23 - $30.50/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Flourish Research is one of the industry's most progressive and diversified clinical trial organizations, with strong capabilities across cardiology, metabolic disorders, renal, oncology, CNS ...

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Clinical Trial information

See Boca Raton, FL salary details

$27

$59

$91

How much do clinical trial jobs pay per hour?

As of Aug 14, 2026, the average hourly pay for clinical trial in Boca Raton, FL is $59.33, according to ZipRecruiter salary data. Most workers in this role earn between $48.12 and $66.83 per hour, depending on experience, location, and employer.

What are clinical trials?

Clinical trials are research studies that involve human participants and are designed to evaluate the safety and effectiveness of new medical treatments, drugs, or devices. These trials follow a carefully controlled protocol and are conducted in phases to systematically assess outcomes. Participants may include patients with specific medical conditions or healthy volunteers, depending on the study's goals. The results from clinical trials help inform medical decisions and regulatory approvals for new therapies.

What are the key skills and qualifications needed to thrive in a clinical trial role?

To thrive in a Clinical Trial role, you need a solid understanding of clinical research principles, regulatory compliance, and data management, usually supported by a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) certification, and clinical trial management software is typically required. Strong attention to detail, organizational abilities, and effective communication skills help professionals coordinate complex processes and collaborate with interdisciplinary teams. These competencies are vital to ensure trials are conducted ethically, efficiently, and in compliance with regulatory standards.

What jobs are there in clinical trials?

Jobs in clinical trials include clinical research coordinators, clinical research associates, data managers, regulatory affairs specialists, and study nurses. These roles involve tasks such as patient recruitment, data collection, monitoring trial progress, and ensuring compliance with regulations, often requiring knowledge of Good Clinical Practice (GCP) and relevant certifications. The work environment is typically a research site, hospital, or pharmaceutical company, with schedules varying from standard to flexible hours depending on the role.

What are some common challenges faced by professionals working in clinical trial management, and how can they be addressed?

Professionals in clinical trial management often encounter challenges such as adhering to strict regulatory requirements, managing complex timelines, and ensuring effective communication among multidisciplinary teams. Overcoming these challenges typically involves thorough planning, continuous training on regulatory updates, and the use of project management tools to track progress and coordinate tasks. Building strong relationships with investigators and fostering open communication can also help address issues quickly and maintain trial integrity.

How to get into a clinical trial career?

A career in clinical trials typically requires a background in healthcare, life sciences, or related fields, along with knowledge of Good Clinical Practice (GCP) guidelines. Entry-level roles often require a bachelor's degree, and certifications such as the Certified Clinical Research Professional (CCRP) can enhance job prospects. Gaining experience through internships or entry-level positions in research settings is also beneficial.

What are the most commonly searched types of Clinical Trial jobs in Boca Raton, FL?

The most popular types of Clinical Trial jobs in Boca Raton, FL are:

What are popular job titles related to Clinical Trial jobs in Boca Raton, FL?

For Clinical Trial jobs in Boca Raton, FL, the most frequently searched job titles are:

What job categories do people searching Clinical Trial jobs in Boca Raton, FL look for?

The top searched job categories for Clinical Trial jobs in Boca Raton, FL are:

What cities near Boca Raton, FL are hiring for Clinical Trial jobs?

Cities near Boca Raton, FL with the most Clinical Trial job openings:

Clinical Trial jobs near you
Infographic showing various Clinical Trial job openings in Boca Raton, FL as of August 2026, with employment types broken down into 2% As Needed, 72% Full Time, 20% Part Time, and 6% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $123,398 per year, or $59.3 per hour.

Clinical Trial Manager, Immunology

Syncromune

Fort Lauderdale, FL • On-site, Remote

$145K - $165K/yr

Full-time

Posted 24 days ago

Job description

The Clinical Trial Manager (CTM) works closely with various internal team members and vendors as well as clinical sites to ensure that clinical trials are conducted in a timely fashion and in a manner compliant with SOPs, ICH/GCP/regulatory guidelines, company goals, and company timelines. This position is responsible for leading and managing the conduct of complex drug/device combination immuno-oncology clinical trials from study start-up to closeout. The CTM shall serve as the primary contact for clinical site personnel for trial activities and progress, including responding to issues and recommending corrective actions.
Responsibilities:
  • Participates in protocol, CRF and strategy development.
  • Prepares metrics and updates for management, as assigned.
  • Prepares and shares written and verbal reports on the status of clinical trials and significant issues impacting clinical trials.
  • Proactively identifies potential study issues/risks and recommends/implements solutions.
  • Participates in and facilitates CRO/vendor selection process for outsourced activities, as assigned.
  • Manages CRO interactions, including sponsor oversight of operational functional activities.
  • Prepares and/or reviews/approves study-related documents (Monitoring Plan, Communication Plan, Laboratory Manual, Procedures Manual, Pharmacy Manual, CRF Completion Guidelines, etc.).
  • Develop and maintain the Project Team List for assigned clinical trials.
  • Manages clinical monitoring activities ensuring compliance with Good Clinical Practice (GCP) and applicable regulations.
  • Participates in the development, review, and implementation of departmental SOPs and processes.
  • Recommends and implements innovative process ideas to impact clinical trials management.
  • Organizes and manages internal team meetings, investigator meetings, and other trial-specific meetings.
  • Serves as a liaison and resource for investigational sites of assigned studies.
  • Reviews site study documents (informed consent template, study tools/worksheets, etc.).
  • Participates in the training and evaluation of study personnel specific to assigned studies.
  • Performs some or all the duties and responsibilities outlined for Senior Clinical Research Associate, as needed.
  • Oversee and shepherd payments to sites through the payment approval process.
  • All other duties as assigned.

Requirements:
  • Bachelor's degree in life sciences, nursing, pharmacy, or a related field. Additional clinical trial certifications (e.g., ACRP, SOCRA) are a plus.
  • At least 5 years of experience in clinical research, clinical operations, (recent experience as a CRA in oncology; academic site level experience in oncology as a study coordinator is preferred).
  • Familiarity with clinical trial processes, Good Clinical Practice (GCP), and ICH guidelines.
  • Strong experience in oncology clinical trials.
  • Experience with phase I-II oncology studies from study start up through data lock.
  • Solid understanding of GCP, ICH guidelines, and regulatory requirements.
  • Strong scientific acumen and ability to grasp complex scientific and technical concepts.
  • Familiarity with 21CFR, ISO, ICH, GCP, and relevant regulations, standards, directives, and guidance is essential.
  • Excellent analytical and research skills, with a keen eye for detail.
  • Exceptional communication, organizational, and problem-solving skills.
  • Ability to work independently and collaboratively in a fast-paced, deadline-driven matrix environment.
  • Ability to set priorities and accomplish assigned work within deadlines.

Working Conditions:
  • Specify work environment:
  • The work environment shall be split between a virtual office environment and the Company headquarters in Fort Lauderdale, FL.
  • Domestic and International travel up to 30%.
  • Must have current passport or willingness to obtain immediately
  • Must be able to successfully pass a background check, drug testing, and other applicable vendor credentialing requirements
  • Ability to lift up to 35 pounds
  • Regularly required to stand, sit, talk, hear, and use hands
  • Prolonged periods of sitting and standing

Syncromune is an Equal Opportunity Employer.
The Company is required to provide a reasonable estimate of the salary range for this job in certain states and cities within the United States. Final determinations with respect to salary will take into account a number of factors, which may include, but not be limited to, the primary work location and the chosen candidate's relevant skills, experience, and education.
Expected US salary range: $145,000-165,000
This position generally is eligible for cash incentive compensation, equity incentive compensation, and employee benefits under the Company's benefit plans.
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