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Clinical Project Associate Jobs in Florida (NOW HIRING)

Elevance Health

Sr Project Manager

Lake Mary, FL · Hybrid

Through our distinct clinical expertise, digital capabilities, and broad access to specialty ... Associates in these jobs must follow the specific policies, procedures, guidelines, etc. as stated ...

Elevance Health

Sr Project Manager

Lake Mary, FL · Hybrid

Through our distinct clinical expertise, digital capabilities, and broad access to specialty ... Associates in these jobs must follow the specific policies, procedures, guidelines, etc. as stated ...

Alira Health

Clinical Research Associate

Sydney, FL

Summary ROLE The Clinical Research Associate is an important member of the Alira Health Clinical ... CRAs work closely with the In-house CRAs, Lead CRAs, Director of Clinical Monitoring and Project ...

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Clinical Project Associate information

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$9

$23

$41

How much do clinical project associate jobs pay per hour?

As of Jun 12, 2026, the average hourly pay for clinical project associate in Florida is $23.57, according to ZipRecruiter salary data. Most workers in this role earn between $15.82 and $31.06 per hour, depending on experience, location, and employer.

What is a Clinical Project Associate?

A Clinical Project Associate (CPA) is a professional who supports the planning, execution, and management of clinical trials in the pharmaceutical, biotechnology, or medical device industries. Their responsibilities often include coordinating study documentation, assisting with regulatory submissions, tracking project timelines, and facilitating communication among study teams. CPAs play a crucial role in ensuring that clinical trials are conducted efficiently, ethically, and in compliance with regulatory standards. They work closely with clinical project managers, research associates, and other team members to help bring new therapies and treatments to market.

What are the typical responsibilities of a Clinical Project Associate in supporting clinical trial operations?

As a Clinical Project Associate, you will play a vital role in ensuring the smooth execution of clinical trials by handling administrative and logistical tasks. Your responsibilities often include maintaining study documentation, coordinating meetings, tracking project timelines, and supporting communication between internal teams and external partners such as clinical sites and vendors. You may also assist with regulatory submissions and help monitor compliance with study protocols. This position offers excellent exposure to the clinical research process and can be a stepping stone to more advanced roles within clinical operations.

What are the key skills and qualifications needed to thrive as a Clinical Project Associate, and why are they important?

To thrive as a Clinical Project Associate, you need a background in life sciences or a related field, attention to detail, and strong organizational skills. Familiarity with clinical trial management systems (CTMS), regulatory documentation, and tools like Microsoft Office is typically required. Excellent communication, teamwork, and time management abilities help professionals excel in supporting project coordination. These skills are crucial for ensuring regulatory compliance, smooth project execution, and effective collaboration within clinical research teams.

What is the difference between Clinical Project Associate vs Clinical Research Coordinator?

AspectClinical Project AssociateClinical Research Coordinator
CredentialsBachelor's degree often required; certifications like CCRP beneficialBachelor's degree in health or related field; certifications like CCRP common
Work EnvironmentTypically works with project teams, sponsors, and CROs in clinical trial settingsWorks directly with patients, investigators, and site staff at clinical trial sites
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, clinics, research sites
Search & Comparison IntentHigh overlap in responsibilities and certificationsSimilar roles but more patient-facing

The Clinical Project Associate primarily supports clinical trial management from a project perspective, working with sponsors and CROs. In contrast, the Clinical Research Coordinator focuses on patient interactions and site management. Both roles require similar educational backgrounds and certifications, but their work environments and daily tasks differ significantly.

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 Associate jobs in Florida? For Clinical Project Associate jobs in Florida, the most frequently searched job titles are:
What job categories do people searching Clinical Project Associate jobs in Florida look for? The top searched job categories for Clinical Project Associate jobs in Florida are:
What cities in Florida are hiring for Clinical Project Associate jobs? Cities in Florida with the most Clinical Project Associate job openings:
Clinical Project Associate jobs near you
Infographic showing various Clinical Project Associate job openings in Florida as of June 2026, with employment types broken down into 1% As Needed, 76% Full Time, 20% Part Time, 1% Temporary, and 2% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $49,025 per year, or $23.6 per hour.
CLINICAL APPLICATIONS ANALYST II - EPIC PRELUDE ANALYST

CLINICAL APPLICATIONS ANALYST II - EPIC PRELUDE ANALYST

H. Lee Moffitt Cancer Center

Tampa, FL • Remote

Full-time

Posted 29 days ago

Moffitt Cancer Center rating

8.1

Company rating: 8.1 out of 10

Based on 92 frontline employees who took The Breakroom Quiz

70th of 871 rated healthcare providers

Job description

Remote applicants from the following states are encouraged to apply:

Alabama, Arizona, Arkansas, Florida, Georgia, Idaho, Indiana, Iowa, Kansas, Louisiana, Mississippi, Missouri, Montana, North Carolina, Ohio, Oklahoma, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, or Wyoming.

The Clinical Applications Analyst II - Prelude advances Moffitt’s mission to prevent and cure cancer by contributing to the design, implementation, and support of clinical and enterprise applications that improve patient care, research, and operational performance. This mid-level role manages technical solutions for moderately complex projects, collaborates with clinical and operational teams, and provides guidance to junior analysts. By ensuring effective and reliable technology solutions, The Analyst II empowers staff and clinicians to deliver exceptional cancer care and research outcomes.

The Clinical Applications Analyst II will:

  • Plan, design, configure, build, test, implement and maintain clinical and enterprise applications, including moderately complex system components.
  • Troubleshoot multifaceted issues spanning software, hardware, interfaces, and databases.
  • Monitors system performance
  • Perform quality assurance and integrated testing to ensure application reliability and alignment with organizational standards. 
  • Supports projects and develop application-specific enhancements and reports to support clinical and operational priorities.
  • Develops and maintains system documentation for build specifications.
  • Mentor and guide Analyst I team members on technical tasks and processes.
  • Provide 24/7 operational support for assigned applications and participate in on-call rotations as needed.

Minimum Education:

Bachelor’s Degree (Business, IS, Healthcare, or related field of study required)

Associate's Degree + 2 additional years of applicable experience (minimum total of 5 years) will be considered in lieu of Bachelor's degree

Certification:

Epic Certification in Prelude is required. Cadence certification is preferred.

Minimum Experience Required:
3 years of applicable system build experience; high level complexity

Assigned Applications:
Cadence Enterprise Scheduling
Prelude Enterprise Registration

Minimum Skills/Specialized Training Required:

  • Advanced knowledge of application support and development.
  • Experience in project management and team leadership.
  • Strong problem-solving and critical thinking abilities.
  • Experience with workflow analysis or development of application solutions preferred.
  • Experience in building and implementation within Epic applications, other electronic health record applications, and/or healthcare operations background (e.g., clinical, billing, scheduling, access services, health information management, etc.) preferred.
  • Must hold EPIC certification in Prelude. Additional certification in Cadence is preferred.
  • Knowledge of clinical, business, and/or operational healthcare hospital/clinic workflows preferred.
  • Proficient in Microsoft Visio preferred.
  • Strong project management and presentation skills preferred.
  • Professional level certification from an accredited organization in relevant informatics, health information technology, clinical or business specialties preferred.
  • Excellent presentation and documentation skills.

Preferred Experience:

  • Experience with PACS systems preferred.
  • Experience with systems provisioning/security and Active Directory structures preferred.
  • Experience with integration platforms including middleware and application interfaces preferred.
  • Experience working with project life cycle and project management methodologies preferred.
  • Experience with operational workflows of Patient Access functions

Note: Travel to our Tampa, Florida location will be required based on project needs, approximately once a month.

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