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Clinical Research Study Manager Jobs in Boca Raton, FL

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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 Sep 7, 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 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

Clinical Research Coordinator

DERMCARE MANAGEMENT LLC

Hollywood, FL • On-site

$22.25 - $29.50/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 26 days ago

Job description

Clinical Research Coordinator
The Clinical Research Coordinator leads and manages clinical trials in compliance with regulatory standards, working closely with the investigative team, pharmaceutical sponsors, and research participants. This role requires a strong medical background, proficiency in Good Clinical Practices (GCP), FDA regulations, and a commitment to ethical research standards.
Key Responsibilities:
Duties will include, but are not limited to:
  • Manage and oversee the execution of clinical trials under the direction of the Principal Investigator and Site Manager.
  • Conduct patient visits and ensure adherence to study protocols, collecting and processing biological specimens (blood/urine) and performing procedures such as ECGs and vital signs monitoring.
  • Administer questionnaires, diaries, and other participant materials as per protocol.
  • Schedule and coordinate research visits, assessments, and procedures, ensuring all requirements are met.
  • Maintain accurate case report forms, cross-referencing patient medical records for completeness and FDA compliance.
  • Collect, enter, and manage clinical data while maintaining confidentiality.
  • Monitor study participants, ensuring adherence to study guidelines and ethical standards.
  • Manage investigational medications, including receiving, dispensing, and performing drug accountability.
  • Collaborate with laboratories to process, ship, and ensure review of investigational reports.
  • Actively participate in recruiting and screening study participants.
  • Maintain organized records of study materials, ensuring all regulatory documentation is up to date.
  • Ensure necessary supplies and equipment are available and functional for each study.
  • Complying with company policies, HIPAA, OSHA regulations, and Standard Operating Procedures (SOPs) to deliver high-quality services.

Qualifications:
  • High School Diploma or GED
  • Preferred: Bachelor's or master's degree in a related field.
  • Required: Previous experience conducting clinical trials, including recruitment and compliance with regulatory guidelines.
  • Preferred: Certification as a Clinical Research Coordinator (CCRC).
  • Phlebotomy experience and certification where required.
  • Strong knowledge of medical terminology, clinical trial processes, and industry regulations.
  • Proficient with computer hardware and software, including clinical research databases.
  • Proficient in accessing, inputting, and retrieving data from a computer.
  • Strong attention to detail and organizational skills.
  • Ability to prioritize tasks, manage deadlines, and adapt to changing environments.
  • Ability to receive and process information through both oral and written communication.
  • Excellent problem-solving, leadership, and communication skills.
  • Outstanding interpersonal skills, with the ability to establish and maintain effective relationships with patients, investigators, and external partners.
  • Ability to work both independently and collaboratively as part of a team.
  • Ability to maintain confidentiality and handle sensitive information.
  • Willingness to learn and stay updated on new clinical research trends and regulations.
  • CCRC certification a plus.
  • Bi-lingual in Spanish is a plus.

Benefits:
  • Medical Insurance
  • Dental Insurance
  • Vision Insurance
  • Supplemental health benefits
  • Paid time off
  • Holidays
  • Retirement plan (401k)

Physical Demands and Work Environment
  • Ability to sit or stand for 6-8 hours a day and lift or carry 5-10 pounds occasionally.
  • Requires substantial use of wrists, hands, and fingers for tasks such as typing and filing.
  • This position operates primarily in a professional office/clinical environment. The role regularly requires sitting, working at a computer, communicating with employees and managers.

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