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Clinical Project Director Jobs in Florida (NOW HIRING)

Acorn Health

Clinical Director

Miramar, FL · On-site

$90K - $117K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

What our Clinical Directors do: * Responsible for driving the execution of key service, quality and ... Experience managing teams, projects, and meetings * Proficiency with ABA data collection and ...

Acorn Health

Clinical Director

Miramar, FL · On-site

$90K - $117K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

What our Clinical Directors do: * Responsible for driving the execution of key service, quality and ... Experience managing teams, projects, and meetings * Proficiency with ABA data collection and ...

Medix

Clinical Research Site Director

Palmetto Bay, FL · On-site

$52.88 - $64.90/hr

Perform additional duties and special projects as assigned. Qualifications Education & Experience ... Clinical Site Director Position Summary The Clinical Site Director is responsible for the overall ...

Central Florida Health Care

Clinical Pharmacist

Lakeland, FL · On-site

$105K - $125K/yr

... projects * Delivers direct patient care and clinical practice * Assure pharmacy is an integral part of the health-care delivery system and facilitate enhancement and expansion of pharmacy services ...

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 ...

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All JobsClinical Project JobsClinical Project Director JobsClinical Project Director Jobs in Florida

Clinical Project Director information

See Florida salary details

$32.9K

$81.9K

$147.6K

How much do clinical project director jobs pay per year?

As of Aug 13, 2026, the average yearly pay for clinical project director in Florida is $81,875.00, according to ZipRecruiter salary data. Most workers in this role earn between $55,300.00 and $108,000.00 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 Florida?

The most popular types of Clinical Project jobs in Florida are:

What are popular job titles related to Clinical Project Director jobs in Florida?

For Clinical Project Director jobs in Florida, the most frequently searched job titles are:

What job categories do people searching Clinical Project Director jobs in Florida look for?

The top searched job categories for Clinical Project Director jobs in Florida are:

What cities in Florida are hiring for Clinical Project Director jobs?

Cities in Florida with the most Clinical Project Director job openings:

Clinical Project Director jobs near you
Infographic showing various Clinical Project Director 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 $81,875 per year, or $39.4 per hour.

Clinical Research Site Director

Alcanza Clinical Research

Orlando, FL • On-site

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 15 days ago

Job description

Clinical Research Site Director
Department: Operations
Employment Type: Full Time
Location: CNS - Orlando
Reporting To: Susan Angel
Description
Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, VA, SC, TN, TX and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow.
The Clinical Site Director is responsible for driving operational performance for of the research site. Provides on-site oversight to help ensure execution and coordination of clinical research activities according to ICH guidelines, GCP, and FDA guidelines and follows company policies and procedures.
Key Responsibilities
Essential Job Duties:
  • Overall site management and leadership with a focus on driving site performance, enhancing efficiencies, pati,ent safety and protocol/GCP/regulatory compliance.
  • Collaborating with department leaders in Business Development, Patient Recruitment, Finance, and Budgets Contracts and Quality to coordinate delivery expectations, meet expected study milestones (such as site activation targets, enrollment targets, etc.), meet budgets, and delivery quality data to sponsors.
  • Reviewing the performance dashboards and other clinical trial systems to oversee site and patient activities, ensure proper staff coverage, and to ensure the data has been updated to reflect timely execution of all operational aspects (required visits/calls, duration, and frequency).
  • Overseeing resourcing allocations, site assignments and study team members' output and performance, to ensure study deliverables are on track, identifying risks to delivery or quality, and escalating any risks to clinical trial management deliverables (timeline, quality and budget).
  • Assisting with initial and ongoing trainings regarding protocol specificities, Case Report Form (CRF) completion, Standard Operating Procedures (SOPs), clinical plans and guidelines, and timelines for the study.
  • Ensuring adherence to standard operating procedures, good clinical practice (GCP), FDA regulations, and company policies and procedures.
  • Overseeing site staff assigned to the study and routinely assessing study-specific process and training compliance, CMP compliance, and identifies emerging risks.
  • Develop and support execution of corrective action plans at site and study level.
  • Overseeing people management activities including interviewing and selection, performance appraisals, job description preparation, employee counseling, career coaching and termination meetings. Managing site staff, proactively identify and resolve issues, and work to ensure successful site operations.
  • Overseeing all payroll, absence tracking/approvals, new hire orientation, and training per operational needs.
  • Collaborating with investigators to ensure patient safety and meeting client goals and timelines.
  • Employing strategic thinking and problem-solving skills to propose and implement risk mitigations.
  • Participating and presenting in management or site meetings.
  • Perform all other duties as required or assigned.

Skills, Knowledge and Expertise
Minimum Qualifications: A Bachelor's degree AND 5+ years of clinical research experience or an equivalent combination of education and experience is required. 2+ years of clinical research site management experience is required. Bi-lingual (English / Spanish) proficiency is preferred.
Required Skills:
  • Proficiency with computer applications such as Microsoft applications, email, electronic health records, web applications, and the ability to type proficiently (40+ wpm).
  • Must possess strong organizational, time management, problem solving, and project management skills to meet project deadlines.
  • Well-developed written and verbal communication skills.
  • Well-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, subjects, managers and external customers.
  • Ability to effectively handle multiple tasks and adapt to changes in workloads and priorities.
  • Must be professional, respectful of others, self-motivated, and have a strong work ethic.
  • Must possess a high degree of integrity and dependability.
  • Ability to work under minimal supervision, identify problems and implement solutions.
  • Ability to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.

Benefits
  • Full-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire.
  • Medical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.

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