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Clinical Project Manager Jobs in Brandon, FL (NOW HIRING)

TLS Management Inc

Project Manager

Riverview, FL · On-site

Position Summary The Project Manager is responsible for the complete and successful delivery of ... and clinical departments. * Comply with The Joint Commission, NFPA 101 Life Safety Code, NFPA 99 ...

TLS Management Inc

Project Manager

Riverview, FL · On-site

Position Summary The Project Manager is responsible for the complete and successful delivery of ... and clinical departments.Comply with The Joint Commission, NFPA 101 Life Safety Code, NFPA 99 ...

TLS Management Inc

Project Manager

Riverview, FL · On-site

Position Summary The Project Manager is responsible for the complete and successful delivery of ... and clinical departments.Comply with The Joint Commission, NFPA 101 Life Safety Code, NFPA 99 ...

Abbott

Implementation Project Manager

Tampa, FL · Remote

Technical and Clinical expertise and pre-close sales support expansion of base business Tasks ... Ability to manage a project with multiple stakeholders and process owners and clearly, concisely ...

Abbott

Implementation Project Manager

Tampa, FL · Remote

Technical and Clinical expertise and pre-close sales support expansion of base business Tasks ... Ability to manage a project with multiple stakeholders and process owners and clearly, concisely ...

EmergencyMD

Project Manager

Saint Petersburg, FL · On-site

$70 - $110/hr

Emede Electric is seeking an experienced Electrical Project Manager to oversee a variety of electrical manufacturing projects, from interpreting owner specifications to developing detailed production ...

New

Quiet Professionals LLC

Project Manager

Tampa, FL · On-site

Position Summary The Project Manager supports mission-critical objectives under the referenced work order by managing specific Work Order execution, tracking schedules, and mitigating risks to ensure ...

Endurion

Project Manager

Tampa, FL · On-site

$85 - $110/hr

Project Manager Full Time Professional TAMPA, FL, US 6 days ago Requisition ID: 1047 Position Summary The Project Manager supports mission-critical objectives under the referenced work order by ...

New

Full pipeline staffing llc

Project Manager

Tampa, FL · On-site

$140K - $160K/yr

We are seeking a Senior Project Manager with expertise in large scale Multi-Family projects to join an expanding team. Job Summary: Lead teams to complete ground up commercial construction projects ...

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All JobsClinical Project JobsClinical Project Manager JobsClinical Project Manager Jobs in Brandon, FL

Clinical Project Manager information

See Brandon, FL salary details

$25

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How much do clinical project manager jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for clinical project manager in Brandon, FL is $52.75, according to ZipRecruiter salary data. Most workers in this role earn between $36.78 and $61.83 per hour, depending on experience, location, and employer.

What does a clinical project manager do?

A clinical project manager, or CPM, manages clinical trial studies for new drugs and medical devices. In this clinical management position, responsibilities and duties include working with all team members and all aspects of a clinical project, including subject selection and enrollment, record keeping, process auditing, and documentation. They also work with the budget and communicate with third parties, such as laboratories or investigators.

What does a clinical project manager do?

A Clinical Project Manager oversees the planning, execution, and completion of clinical trials in the pharmaceutical, biotechnology, or medical device industries. They coordinate teams, manage budgets, timelines, and ensure that studies comply with regulatory standards and company protocols. Clinical Project Managers act as the main point of contact between sponsors, vendors, and clinical research sites, working to ensure that trials progress smoothly and data integrity is maintained. Their role is critical in bringing new therapies and treatments to market safely and efficiently.

What are the key skills and qualifications needed to thrive as a clinical project manager, and why are they important?

To thrive as a Clinical Project Manager, you need expertise in clinical trial management, regulatory compliance, and a relevant life sciences degree, often supported by experience in clinical research. Familiarity with project management tools, electronic data capture (EDC) systems, and certifications like PMP or ACRP are highly valued. Strong leadership, problem-solving, and communication skills help you effectively coordinate teams and stakeholders. These competencies ensure successful trial execution, regulatory adherence, and timely project delivery in a highly regulated environment.

What are some common challenges clinical project managers face when coordinating multi-site clinical trials?

Clinical Project Managers often encounter challenges such as maintaining consistent communication across different sites, ensuring adherence to regulatory guidelines, and managing timelines amidst unexpected delays. Coordinating multi-site trials requires balancing the needs of diverse teams, addressing site-specific issues, and ensuring data quality across all locations. Effective project management tools, regular status meetings, and proactive risk assessment are essential for overcoming these obstacles and keeping the study on track.

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

AspectClinical Project ManagerClinical Research Associate
CredentialsTypically requires a Bachelor's degree in life sciences, with many holding advanced degrees or certifications like PMPUsually holds a Bachelor's degree in life sciences or related field; certifications like CRA certification are common
Work EnvironmentManages multiple clinical trials, oversees teams, and coordinates with sponsors and sitesMonitors clinical sites, ensures protocol compliance, and collects data
Employer & Industry UsageFound in pharmaceutical, biotech, and CRO companies overseeing entire projectsPrimarily employed by CROs and sponsors to monitor trial sites

The Clinical Project Manager and Clinical Research Associate roles are closely related but differ mainly in scope. The Clinical Project Manager oversees entire clinical trials, manages teams, and coordinates with stakeholders, while the Clinical Research Associate focuses on monitoring clinical sites and ensuring protocol adherence. Both roles require similar educational backgrounds and certifications, but their responsibilities and work environments differ significantly.

How much do clinical project managers earn?

Clinical project managers typically earn between $80,000 and $130,000 annually, depending on experience, location, and the size of the organization. Senior roles or those with specialized skills and certifications can earn higher salaries, often exceeding $150,000. Compensation may also include bonuses and benefits related to project scope and complexity.
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The most popular types of Clinical Project jobs in Brandon, FL are:

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The top searched job categories for Clinical Project Manager jobs in Brandon, FL are:

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Clinical Project Manager jobs near you
Infographic showing various Clinical Project Manager job openings in Brandon, FL as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $109,712 per year, or $52.7 per hour.

Clinical Trial Assistant- Minnesota

FloodGate Medical

Tampa, FL • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 16 days ago

Job description

"At Mobius, we only hire the best of the best. Our people are the primary reason for our success and the first pillar of our core values. As a leading CRO managing clinical trials across the USA, Australia, and New Zealand, we support a diverse portfolio of global and local clients across all phases of development and an array of therapeutic goods. We are committed to supporting our partners through every step of the clinical project journey, from rapid start-ups and comprehensive monitoring to precise data management, in-house EDC, and expedited study close-out."
Job Description
The Clinical Trials Assistant (CTA) role at Mobius Medical is an entry level position into a career in clinical research. The CTA is responsible for providing administrative and organisational support under direction to the clinical trials team. This includes assisting with study start-up activities, communicating with study sites, assisting with monitoring activities, and supporting data management. The CTA will work closely with the Clinical Project Manager and other team members to ensure compliance with ICH-GCP guidelines, as well as national and international regulations. In a training capacity, the CTA will be mentored by colleagues and delegated project-related tasks as part of hands-on training.
Minimum Requirements
  • Bachelor's degree in life sciences, healthcare, or a related field.
  • Basic familiarity with ICH-GCP guidelines and regulatory requirements for clinical trials.
  • Strong organisational and time management skills.
  • Excellent interpersonal and communication skills, both written and verbal.
  • Proficient in Microsoft Office applications (Word, Excel, PowerPoint, Outlook).
  • Ability to work both independently and collaboratively within a team setting.
  • Attention to detail and a commitment to maintaining high-quality work.

Job Requirements
  • Study Start-Up Support:
    • Assist with the development of clinical trial materials, e.g. trial master file build, patient binders, filing.
    • Assist the clinical team with the organisation and execution of site initiation visits, where appropriate.
  • Regulatory and Ethics Submissions:
    • Support the preparation and submission of regulatory documents where appropriate and with supervision.
    • Assist with ethics committee submissions under supervision of CRA or higher, ensuring compliance with applicable guidelines.
  • Site Coordination and Communication:
    • Communicate and coordinate with study sites regarding study shipments of binders and medical devices, including tracking information and record keeping
    • Assist with the collection, review and filing of essential documents from study sites.
    • Attend co-monitoring visits with a (Senior) Clinical Research associate or higher clinical staff member for hands-on training
  • Study Material Preparation and Review:
    • Assist with the preparation of documents and study-related materials under supervision of CRA or higher
    • Perform regular document quality control checks.
  • Data Management:
    • Support the study team with data entry and data cleaning activities under supervision of CDM or higher
    • Assist with Electronic Data Capture (EDC) system validations under supervision of CDM or higher.
  • General Administrative Support:
    • Assist with the preparation of presentations and tools for internal and external stakeholders.
    • Perform other administrative tasks as assigned by CRA, Project Lead (PL) or other team members.
    • Attend project meetings to take minutes, actions and distribute to PL.
  • Professional Development:
    • Stay current with industry trends, best practices, and regulatory updates through continuous learning and professional development opportunities.
    • Attend relevant training courses, workshops, and conferences to enhance job-related skills and knowledge.
    • Share acquired knowledge and expertise with team members to support a culture of continuous improvement within the organization.
  • Occupational Health and Safety:
    • Adhere to Mobius Medical's health and safety policies and procedures to maintain a safe working environment for all employees.
    • Comply with OH&S legislation and operate in accordance with established OH&S practices and procedures.
    • Promote a culture of safety awareness within the clinical trials team and study sites.
    • Identify and report potential hazards, incidents, and safety concerns to the appropriate personnel in a timely manner.
    • Complete required health and safety training to ensure compliance with company and regulatory requirements.

Location
  • Minnesota (Minneapolis preferred), open to near locations

Compensation:
  • Competitive base salary, depending on experience
  • Benefits: Medical, dental, vision - company pays 70% of the premium
  • 160 hours of PTO and 48 hours of sick leave annually
  • 401k match 4%

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