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Clinical Trials Director Jobs in Boca Raton, FL (NOW HIRING)

Segal Trials

Clinical Research Coordinator

Lauderhill, FL · On-site

$24 - $32/hr

... on all trials per company SOP and interface with QA Director as needed Recruitment Responsibilities · Provide weekly updates to Active Studies Report · Communicate all advertising needs to ...

New

Segal Trials

Clinical Research Coordinator

Hollywood, FL · On-site

$22.25 - $29.50/hr

... on all trials per company SOP and interface with QA Director as needed Recruitment Responsibilities · Provide weekly updates to Active Studies Report · Communicate all advertising needs to ...

New

Flourish Research

Site Director

Boca Raton, FL · On-site

In clinical trials and healthcare, excellence means everyone deserves the best care, regardless of their race, color, gender identity, religion, ethnicity, physical abilities, age, sexual orientation ...

Flourish Research

Site Director

Boca Raton, FL · On-site

In clinical trials and healthcare, excellence means everyone deserves the best care, regardless of their race, color, gender identity, religion, ethnicity, physical abilities, age, sexual orientation ...

Flourish Research

Site Director

Boca Raton, FL

In clinical trials and healthcare, excellence means everyone deserves the best care, regardless of their race, color, gender identity, religion, ethnicity, physical abilities, age, sexual orientation ...

micro1 AI

Director of Biostatistics

West Palm Beach, FL · Remote

$60 - $65/hr

Preferred Qualifications * 5+ years as a biostatistician supporting clinical trials at a sponsor, CRO, or academic trials unit. * Hands-on experience producing or quality controlling TFLs for ...

micro1 AI

Director of Biostatistics

Miramar, FL · Remote

$60 - $65/hr

Preferred Qualifications * 5+ years as a biostatistician supporting clinical trials at a sponsor, CRO, or academic trials unit. * Hands-on experience producing or quality controlling TFLs for ...

micro1 AI

Director of Biostatistics

Fort Lauderdale, FL · Remote

$60 - $65/hr

Preferred Qualifications * 5+ years as a biostatistician supporting clinical trials at a sponsor, CRO, or academic trials unit. * Hands-on experience producing or quality controlling TFLs for ...

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Clinical Trials Director information

See Boca Raton, FL salary details

$9

$51

$110

How much do clinical trials director jobs pay per hour?

As of Aug 24, 2026, the average hourly pay for clinical trials director in Boca Raton, FL is $51.56, according to ZipRecruiter salary data. Most workers in this role earn between $30.82 and $67.98 per hour, depending on experience, location, and employer.

What does a clinical trials director do?

A Clinical Trials Director oversees the planning, execution, and management of clinical research trials to ensure they are conducted ethically, safely, and in compliance with regulatory standards. They coordinate with cross-functional teams, manage budgets and timelines, and ensure that trials meet scientific and operational objectives. Their responsibilities also include liaising with regulatory agencies, monitoring trial progress, and addressing any issues that arise during the study.

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

To thrive as a Clinical Trials Director, you need a strong background in clinical research, regulatory compliance, and project management, typically supported by an advanced degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), Good Clinical Practice (GCP) guidelines, and certifications like ACRP or SOCRA are commonly required. Exceptional leadership, strategic thinking, and communication skills are crucial for managing cross-functional teams and stakeholder relationships. These competencies ensure successful trial execution, regulatory adherence, and the delivery of safe and effective clinical outcomes.

What are some common challenges faced by a clinical trials director and how can they be managed?

Clinical Trials Directors often encounter challenges such as coordinating large, cross-functional teams, ensuring strict regulatory compliance, and managing tight timelines for multiple studies. Effective communication, strong leadership, and proactive risk management are essential to address these issues. Staying updated on regulatory changes and fostering collaboration between departments can also help streamline processes and ensure trials run efficiently.

What is the difference between Clinical Trials Director vs Clinical Research Manager?

AspectClinical Trials DirectorClinical Research Manager
ResponsibilitiesOversees entire clinical trial programs, manages teams, and ensures regulatory complianceManages daily operations of clinical research projects, coordinates activities, and supports trial execution
Required CredentialsTypically requires a clinical research or life sciences degree, with extensive experienceRequires similar degrees and experience, often with less strategic oversight
Work EnvironmentSenior leadership in pharmaceutical or biotech companies, overseeing multiple projectsOperational roles within research sites or CROs, focusing on project execution

The Clinical Trials Director focuses on strategic oversight and leadership of clinical trial programs, while the Clinical Research Manager handles day-to-day project management. Both roles require relevant credentials and industry experience, but differ in scope and level of responsibility.

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:

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

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

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

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

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

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

Clinical Trials Director jobs near you
Infographic showing various Clinical Trials Director job openings in Boca Raton, FL as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 19% Part Time, and 7% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $107,242 per year, or $51.6 per hour.

Clinical Research Coordinator

Segal Trials

Lauderhill, FL • On-site

$24 - $32/hr

Other

Posted 2 days ago

New

Job description

The Clinical Research Coordinator is responsible for managing clinical trial performance and ensuring the conduct of their clinical trials is congruent with the vision and mission of the company. The CRC plans, coordinates, evaluates, and manages the care of both the participants and the data for their assigned trials. The CRC follows study specific protocol guideline and communicates and interacts with Investigators, clinic staff, CROs and Sponsors to effectively perform clinical research and coordinate research activities. All duties carried out by the CRC are done in accordance with company policies, SOPs, and Good Clinical Practice (GCP) as well as all applicable local, state, and federal regulations.

Primary Responsibilities

· Coordinate clinical trials conducted by a supervising Principal Investigator in accordance with FDA, GCP and protocol guidelines.

· Identify potential problems or inconsistencies and take action as appropriate.

· Articulate protocol issues to CRO and/or Sponsor, Site Lead, Manager, Principal or Sub-Investigator, and other members of the study team.

· Collect initial subject health and demographic information by interviewing subjects and accessing other appropriate sources.

· Review subject comprehensive medical documentation to determine protocol eligibility under the supervision of the Principal Investigator.

· Ensure a flow of communication including telephone conferences between subject, study staff, referral sources and recruitment team, Sponsor and/or CRO, Monitor(s) and Auditors, if applicable.

· Perform clinical tasks including, but not limited to vital signs, height and weight, ECG, phlebotomy, specimen processing and packaging.

· Dispense and maintain accurate records of investigational and study product.

· Educate subject and family members regarding specific studies and clinical drug trials in general.

· Complete all monitor and sponsor queries in a timely manner.

· Perform some phlebotomy

· Perform Quality Control (QC) checks on all trials per company SOP and interface with QA Director as needed

Recruitment Responsibilities

· Provide weekly updates to Active Studies Report

· Communicate all advertising needs to recruitment team

· Maintain weekly communication with recruitment team to maximize recruitment in all enrolling trials

Minimum Qualifications:

  • At least 2 yrs of experience as a CRC in clinical research or relevant clinical role
  • CCRC or CCRP certification preferred

Perform other duties as assigned. The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive.

Report to duty at physical locations other than the primary assigned location(s) on an as-needed basis. The fluctuating nature of the industry and the existence of multiple physical business addresses mean that employees must be prepared to adjust work location within reason as dictated by business needs.


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