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Clinical Research Study Manager Jobs in Boca Raton, FL

Ambrosia Behavioral Health

Research Assistant

West Palm Beach, FL

$18.50 - $25.75/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

The ideal candidate has hands-on clinical research experience, strong knowledge of research operations and GCP, and the ability to independently manage study activities, participants, documentation ...

GNP Research

Clinical Research Coordinator

Cooper City, FL

$22.25 - $29.50/hr

GNP Research is seeking an experienced Clinical Research Coordinator (CRC) to lead and manage clinical trials across various therapeutic areas. The ideal candidate is detail-oriented, proactive, and ...

GNP Research

Clinical Research Coordinator

Cooper City, FL

$22.25 - $29.50/hr

GNP Research is seeking an experienced Clinical Research Coordinator (CRC) to lead and manage clinical trials across various therapeutic areas. The ideal candidate is detail-oriented, proactive, and ...

Headlands Research

Research Assistant

Lake Worth, FL

$17 - $23.50/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... clinical trial visits in compliance with study protocols * Collect and record vital signs , make ... Strong attention to detail, time management, and ability to work in a fast-paced, regulated ...

New

CenExel

Medical Assistant (Clinical Research)

Hollywood, FL · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

CenExel is a leading nationwide clinical research site and patient network serving the life ... Leading in CNS and early phase studies, our 18 science-led Centers of Excellence deliver the right ...

Headlands Research

Research Assistant

Lake Worth, FL · On-site

$17 - $23.50/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... clinical trial visits in compliance with study protocols * Collect and record vital signs , make ... Strong attention to detail, time management, and ability to work in a fast-paced, regulated ...

New

Research Centers of America, LLC

Clinical Rater

Hollywood, FL · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

We focus on quality people, teamwork, and highly experienced clinical research managers with a ... Administers clinical rating scales on study participants to confirm diagnosis and determine current ...

CenExel

PRN - Clinical Research RN I

Hollywood, FL · On-site

PRN-Clinical Research RN I CenExel is a leading nationwide clinical research site and patient ... Leading in CNS and early phase studies, our 18 science-led Centers of Excellence deliver the right ...

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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?

The top searched job categories for Clinical Research Study Manager jobs in Boca Raton, FL are:

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

Medical Assistant (Clinical Research)

Research Centers of America

Hollywood, FL • On-site

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 5 days ago

Job description

About us:
CenExel is a leading nationwide clinical research site and patient network serving the life sciences industry. Leading in CNS and early phase studies, our 18 science-led Centers of Excellence deliver the right patients, at the right time, in the right place. Recently acquired by BayPine Capital Partners, our research sites provide unparalleled medical and scientific support in the design and execution of clinical trials. Our world-class PIs, advanced patient engagement strategies, premium data analytics, and integrated operations optimize every step of the clinical trial process.
Along with an exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance, CenExel Clinical Research also provides highly competitive compensation and a generous benefits package to full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k.
Job Summary:
With moderate oversight, the Research Assistant I provides direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and site guidelines and policies.
Essential Responsibilities and Duties:
  • Creating and maintaining patient charts for all assigned studies.
  • Preparing participant visits based on CRCs schedule, ensuring all source documents, assessments, lab kits and other visit materials are available and accurate. Filing of lab results, EKG results, and other communication in designated patient charts.
  • Maintaining inventory of study specific supplies including lab kits, assessments and participant facing materials.
  • Timely completion of data entry and query resolution for all CRFs, based on sponsor specific timelines and deadlines established in contract or other communication.
  • Conducts assessments, including but not limited to, blood pressure, urine collection.
  • Communicating with study participants, caregivers, third party vendors and laboratories as needed.
  • Assisting Coordinators with scheduling, copying, faxing, and other clerical tasks.
  • Aiding Coordinators in the facilitation of study monitoring visits.
  • Completion of daily responsibilities delegated by CRC as they pertain to the study and/or participants.
  • Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.

Education/Experience/Skills:
  • High school graduate or equivalent.
  • Must be able to effectively communicate verbally and in writing in English and Spanish.
  • Excellent computer skills and advanced knowledge of electronic equipment (i.e., e-mail, computer, fax machine, copier, etc.).
  • Skilled in organization and record maintenance.
  • Skilled in developing and maintaining effective working relationships with supervisors and co- workers.
  • Strong personal initiative and attention to detail.
  • Ability to react calmly and effectively in emergency situations.
  • Ability to interpret, adapt and apply guidelines and procedures.
  • Ability to clearly communicate both orally and verbally.

Working Conditions
  1. Indoor, Office environment.
  2. Essential physical requirements include sitting, typing, standing, and walking.
  3. Lightly active position, occasional lifting of up to 20 pounds and/or pushing carts up to 50 pounds
  4. Reporting to work, as scheduled, is essential.
  5. On site work arrangement.

CenExel Clinical Research is an Equal Opportunity Employer. All applicants will be considered for employment without regards to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or status.
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

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