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Clinical Project Director Jobs in Boca Raton, FL

ClinDCast LLC

Epic Program Director

Delray Beach, FL · On-site

Epic Program Director - Inpatient Experience Job Summary: Seeking a dynamic Epic Program Director ... clinical settings. This role will oversee end-to-end Epic project lifecycle, ensuring alignment ...

Humana

Director, IT PMO - Segments

Fort Lauderdale, FL · Hybrid

... clinical operations * 4+ years leadership experience in a PMO Preferred Qualifications * Experience working with teams that support architecture, infrastructure, cloud, service, API, Storage ...

Humana

Director, IT PMO - Segments

Fort Lauderdale, FL · Hybrid

... clinical operations * 4+ years leadership experience in a PMO Preferred Qualifications * Experience working with teams that support architecture, infrastructure, cloud, service, API, Storage ...

Humana

Director, IT PMO - Segments

Fort Lauderdale, FL · Hybrid

... clinical operations * 4+ years leadership experience in a PMO Preferred Qualifications * Experience working with teams that support architecture, infrastructure, cloud, service, API, Storage ...

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All JobsClinical Project JobsClinical Project Director JobsClinical Project Director Jobs in Boca Raton, FL

Clinical Project Director information

See Boca Raton, FL salary details

$41.8K

$104K

$187.4K

How much do clinical project director jobs pay per year?

As of Jul 17, 2026, the average yearly pay for clinical project director in Boca Raton, FL is $103,971.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,200.00 and $137,100.00 per year, depending on experience, location, and employer.

What is the difference between Clinical Project Director vs Clinical Project Manager?

AspectClinical Project DirectorClinical Project Manager
ResponsibilitiesOversees multiple projects, strategic planning, high-level decision makingManages individual projects, coordinates teams, ensures project milestones
Required CredentialsTypically requires a clinical research degree, extensive experience, and certifications like PMPRequires a relevant degree, experience in clinical trials, and often PMP or similar certifications
Work EnvironmentSenior leadership in pharmaceutical or biotech companies, CROsProject teams within clinical research organizations or pharmaceutical companies

The Clinical Project Director focuses on strategic oversight and managing multiple projects at a higher level, while the Clinical Project Manager handles day-to-day project execution and team coordination. Both roles require relevant clinical research experience and certifications, but the Director role involves broader responsibilities and strategic planning.

What are the most commonly searched types of Clinical Project jobs in Boca Raton, FL? The most popular types of Clinical Project jobs in Boca Raton, FL are:
What job categories do people searching Clinical Project Director jobs in Boca Raton, FL look for? The top searched job categories for Clinical Project Director jobs in Boca Raton, FL are:
What cities near Boca Raton, FL are hiring for Clinical Project Director jobs? Cities near Boca Raton, FL with the most Clinical Project Director job openings:
Clinical Project Director jobs near you
Infographic showing various Clinical Project Director job openings in Boca Raton, FL as of July 2026, with employment types broken down into 2% As Needed, 74% Full Time, 17% Part Time, 1% Temporary, and 6% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $103,971 per year, or $50 per hour.
Director, Clinical Research

Director, Clinical Research

Life Extension Foundation Buyers Club Inc

Fort Lauderdale, FL • On-site

Full-time

Re-posted 12 days ago

Job description

General Description: Leads Life Extension Clinical Research and ensures studies are conducted in a timely, quality driven manner while following all applicable guidelines. This role is responsible for the day-to-day operations of Life Extension Clinical Research, including managing clinical studies (onsite and virtual) with a sense of urgency, within budget and with the goal of creating a Clinical Center of Excellence.

Core Duties and Responsibilities:

  • Provides overall leadership to LECR and staff by clearly communicating goals and expectations and driving productivity with a sense of urgency while ensuring 100% compliance with rules and regulations.
  • Ensure all clinical trial projects (internal and external), to include project management, tracking and reporting trial progress and monitoring test item expiration dates in relation to project timelines
  • Management and oversight of research projects and laboratory components of studies; develops appropriate study design and establishes accurate timelines; collaborates on statistical plans and data analysis
  • Prepares and/or supervises the preparation of the Protocol, Informed Consent and associated documentation for clinical studies and assures necessary project approvals from an Institutional Review Board (IRB) are obtained
  • Primary point of contact for the IRB
  • Prepares and manages all LE Clinical Research budgets
  • Sets priorities for all staff to assure project timelines are met, including active promotion of clinical research initiatives, i.e. use of social media
  • Assures all applicable regulations are implemented and followed; supervises management of data files and confidential information; follows established SOPs, i.e. for appropriate document destruction
  • Responds to inquiries from individuals seeking funding or product donations, and if warranted, presents project and recommendations to administration
  • Monitors progress of ongoing external projects that received Life Extension support and/or donated materials, assuring resupply so materials do not expire without replacement during a project
  • Supports the study team with the various tasks associated with conducting the clinical trial to ensure goals are met
  • Seeks out ways to employ innovative technology to optimize organization and individual efficiency and performance
  • Proactively drives the effort to achieve the goal of creating an impactful Clinical Center of Excellence.
  • Hires, trains and assures high quality supervision of the LE clinical research staff
  • 2 onsite days per week is an essential function of this position with flexibility to work additional onsite days as needed
  • Travels as needed
  • Additional duties as assigned

Position Requirements:

  • Bachelor’s degree in Biomedical Science, Healthcare or a Life Science related field required; Advanced degree (MSN/NP, MD, DO, PharmD, MHSA, PhD) preferred
  • 7+ years Clinical Research experience with at least 2 years in a supervisory leadership capacity preferred
  • Demonstrated leadership, ability to effectively communicate and drive positive change
  • Equally adept at running traditional in person and innovative virtual clinical studies.
  • Proactively manage LECR and readily adapt to and incorporate new technologies and platforms
  • Successfully multi-task in an entrepreneurial environment and manage multiple clinical studies in parallel