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Clinical Research Study Manager Jobs in Boca Raton, FL

Flourish Research

Clinical Research Coordinator

Boca Raton, FL · On-site

$23 - $30.50/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

About Us Flourish Research is where clinical trials thrive. Flourish Research is one of the ... Maintain and document communication with Leads, Managers, PIs/Sub-Is, and study team per protocol ...

Flourish Research

Clinical Research Coordinator

Boca Raton, FL · On-site

$23 - $30.50/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

About Us Flourish Research is where clinical trials thrive. Flourish Research is one of the ... Maintain and document communication with Leads, Managers, PIs/Sub-Is, and study team per protocol ...

Flourish Research

Clinical Research Coordinator

Boca Raton, FL · On-site

$23 - $30.50/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

About Us Flourish Research is where clinical trials thrive. Flourish Research is one of the ... Maintain and document communication with Leads, Managers, PIs/Sub-Is, and study team per protocol ...

Flourish Research

Clinical Research Coordinator

Boca Raton, FL · On-site

$23 - $30.50/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

About Us Flourish Research is where clinical trials thrive. Flourish Research is one of the ... Maintain and document communication with Leads, Managers, PIs/Sub-Is, and study team per protocol ...

Flourish Research

Clinical Research Coordinator

Boca Raton, FL · On-site

$23 - $30.50/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

About Us Flourish Research is where clinical trials thrive. Flourish Research is one of the ... Maintain and document communication with Leads, Managers, PIs/Sub-Is, and study team per protocol ...

Flourish Research

Clinical Research Coordinator

Boca Raton, FL · On-site

$23 - $30.50/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

About Us Flourish Research is where clinical trials thrive. Flourish Research is one of the ... Maintain and document communication with Leads, Managers, PIs/Sub-Is, and study team per protocol ...

Health Haven

Clinical Research Coordinator

West Palm Beach, FL · On-site

$25 - $35/hr

  • Medical

  • Dental

  • Vision

  • Life

  • PTO

Data Collection & Management: Accurately collect, document, and enter study data into electronic ... Support additional clinical research activities and operational needs as required What You'll Bring

Health Haven

Clinical Research Coordinator

West Palm Beach, FL

$25 - $35/hr

  • Medical

  • Dental

  • Vision

  • Life

  • PTO

... study progress and resolve inquiries Data Collection & Management: Accurately collect, document ... Support additional clinical research activities and operational needs as required What You'll Bring ...

Health Haven

Clinical Research Coordinator

West Palm Beach, FL · On-site

$25 - $35/hr

  • Medical

  • Dental

  • Vision

  • Life

  • PTO

... to support study progress and resolve inquiries • Data Collection & Management: Accurately ... Support additional clinical research activities and operational needs as required What You'll Bring ...

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Showing results 21-40

All JobsClinical Research Study JobsClinical Research Study Manager JobsClinical Research Study Manager Jobs in Boca Raton, FL

Clinical Research Study Manager information

See Boca Raton, FL salary details

$46.5K

$101.9K

$179.4K

How much do clinical research study manager jobs pay per year?

As of Aug 17, 2026, the average yearly pay for clinical research study manager in Boca Raton, FL is $101,858.00, according to ZipRecruiter salary data. Most workers in this role earn between $76,900.00 and $116,200.00 per year, depending on experience, location, and employer.

What does a clinical research study manager do?

A Clinical Research Study Manager oversees the planning, execution, and completion of clinical trials to ensure they are conducted ethically and in compliance with regulatory standards. They coordinate with research teams, manage budgets and timelines, and ensure accurate data collection and reporting. Their role is crucial in ensuring that clinical studies run smoothly and produce reliable results that can be used for regulatory submissions or scientific publications.

What are the key skills and qualifications needed to thrive as a clinical research study manager?

To thrive as a Clinical Research Study Manager, you need expertise in clinical trial management, regulatory compliance, and protocol development, often supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and certifications such as GCP (Good Clinical Practice) are typically required. Strong organizational, leadership, and communication skills help manage cross-functional teams and ensure smooth study execution. These skills and qualifications are crucial for maintaining study integrity, meeting regulatory standards, and delivering successful clinical trial outcomes.

What are some common challenges faced by clinical research study managers in coordinating multi-site studies?

Clinical Research Study Managers often encounter challenges in ensuring consistent protocol adherence and data integrity across multiple study sites. Coordinating communication between site teams, managing timelines, and troubleshooting unexpected issues such as recruitment delays or regulatory hurdles are frequent tasks. Successful managers use strong organizational skills and proactive planning to mitigate these challenges, and often rely on regular meetings and digital tools to keep all stakeholders aligned. Establishing clear processes and fostering open communication are key to overcoming these complexities and ensuring study success.

What is the difference between Clinical Research Study Manager vs Clinical Research Coordinator?

AspectClinical Research Study ManagerClinical Research Coordinator
CredentialsBachelor's degree, often with experience in project managementBachelor's degree in health sciences or related field, certification optional
Work EnvironmentOversees multiple studies, manages teams, and coordinates with sponsorsHandles daily study activities, patient interactions, and data collection
Employer & IndustryPharmaceutical companies, CROs, academic institutionsHospitals, clinics, research sites
Search & Comparison IntentUnderstanding managerial roles, responsibilities, and qualificationsFocus on operational tasks and patient management

The Clinical Research Study Manager typically oversees multiple studies, manages teams, and liaises with sponsors, requiring project management skills. In contrast, the Clinical Research Coordinator handles daily study activities, patient interactions, and data collection at research sites. Both roles are essential in clinical research but differ in scope and responsibilities.

What are popular job titles related to Clinical Research Study Manager jobs in Boca Raton, FL?

For Clinical Research Study Manager jobs in Boca Raton, FL, the most frequently searched job titles are:

What job categories do people searching Clinical Research Study Manager jobs in Boca Raton, FL look for?

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What cities near Boca Raton, FL are hiring for Clinical Research Study Manager jobs?

Cities near Boca Raton, FL with the most Clinical Research Study Manager job openings:

Clinical Research Study Manager jobs near you

Clinical Research Assistant

VENTRE MEDICAL ASSOCIATES

Fort Lauderdale, FL

Full-time

Re-posted 9 days ago

Job description

Function: The position trains with other clinical research staff and works directly with physicians to conduct clinical research trials, recruit and consent subjects, and collect and verify accuracy of data. The incumbent also assists in designing clinical trials and skill operationalizing a clinical trial in a clinical study; conducts human subject research involving multiple study sites; ensures IRB compliance; and provides communication to the Principal Investigator. 

Principal Duties & Responsibilities:

  • Assist in data management, regulatory paper works and other local administrative tasks as supervised by the clinical research coordinator
  • Coordinate research and administrative activities, ensuring all projects are completed according to project/study timelines
  • Assist in the development of project/study policies and procedures. Administer policies and procedures according to protocol, Institutional Review Board (IRB), grant/contract and study and site specifications
  • Recruit study participants and complete structured clinical assessments with participants
  • Monitor and promptly respond to participant queries
  • Collect and track study data and compile data reports
  • Submit and maintain proper study records, including submission of timely reports to Institutional Review Boards
  • Produce special and recurring reports


Other Duties as Assigned: 

The above information on this portion is designed to present the most essential duties and responsibilities necessary to achieve the positions end results. The occupant of this position is required to follow any other job-related instructions and perform any other duties as requested by Physician Director(s), Clinical Research Manager, and/or Practice Manager. It is the responsibility of each employee to assist other office staff when and where necessary. All employees have the responsibility of answering phones, maintaining files, filing, updating data, and receiving prescription refill orders, etc. Most importantly, it is each staff member’s responsibility to project and maintain a positive attitude toward all patients and fellow co- workers.  The duties listed may be changed or modified at any time.


 

  • Excellent interpersonal skills to deal effectively with clinicians, patients, administrators, auxiliary personnel, regulators, monitors and sponsors
  • Knowledge of medical terminology
  • Knowledge of good clinical practice, FDA, OHRP, HIPAA policies
  • Familiarity with the Microsoft Office Suite
  • Previous work with CRFs and EDC
  • Excellent organizational skills to independently manage work flow
  • Ability to prioritize quickly and appropriately
  • Ability to multi-task
  • Meticulous attention to detail

Education and Experience:

  • Licensed candidates must have an Associate's degree and RN or LPN licensure
  • One year of experience working in clinical research is preferred
  • Psychology background preferred

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