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Clinical Trial Manager Jobs in Boca Raton, FL (NOW HIRING)

Cleveland Clinic

Research Program Manager

Weston, FL · Hybrid

Serve as the clinical trial management system liaison for the assigned research operation cluster; ensure the proper use and ensure accurate, complete and timely data entry of study demographics and ...

Headlands Research

Research Assistant

Lake Worth, FL · On-site

$17 - $23.50/hr

... of clinical trial execution-from subject screening to data entry. Your work will directly ... Strong attention to detail, time management, and ability to work in a fast-paced, regulated ...

Neara

Data Partnerships Manager

Boca Raton, FL · On-site

$90 - $130/hr

Return to jobs list Data Partnerships Manager Job type: Full Time · Department: Provider ... Familiarity with clinical trial operations and patient recruitment workflows * Existing ...

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All JobsClinical Trial JobsClinical Trial Manager JobsClinical Trial Manager Jobs in Boca Raton, FL

Clinical Trial Manager information

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$91

How much do clinical trial manager jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for clinical trial manager in Boca Raton, FL is $59.33, according to ZipRecruiter salary data. Most workers in this role earn between $48.12 and $66.83 per hour, depending on experience, location, and employer.

What does a clinical trial manager do?

A clinical trial manager, or CTM, oversees research and each phase of clinical drug tests at a hospital. They work closely with both the doctors and clinicians who are performing the trial, as well as the sponsor of the study, which is typically a pharmaceutical company or other health care organization. As a CTM, duties and responsibilities include planning and managing the trial, making sure that the test meets all government standards, and determining if it was successful. Clinical trial managers also hire, train, and evaluate the members of the clinical team.

What does a clinical trial manager do?

A Clinical Trial Manager oversees the planning, coordination, and execution of clinical trials for new drugs, medical devices, or treatments. They ensure that trials are conducted in compliance with regulatory guidelines, company protocols, and ethical standards. Their responsibilities include managing budgets, timelines, and teams, as well as monitoring data quality and safety throughout the study. Clinical Trial Managers also work closely with investigators, sponsors, and regulatory agencies to ensure successful trial outcomes.

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

To thrive as a Clinical Trial Manager, you need a solid background in life sciences, clinical research experience, and often a relevant bachelor's or master's degree. Familiarity with clinical trial management systems (CTMS), regulatory requirements like GCP, and certifications such as ACRP or SOCRA are highly beneficial. Strong organizational skills, attention to detail, leadership, and effective communication are critical soft skills for managing teams and stakeholders. These skills ensure trials are conducted ethically, efficiently, and compliantly, leading to successful study outcomes.

What are some common challenges clinical trial managers face when coordinating multi-site studies?

Clinical Trial Managers often encounter challenges such as ensuring consistent protocol implementation across different sites, managing timelines in the face of site-specific delays, and maintaining clear communication among diverse teams. They must also navigate regulatory differences between regions and address unforeseen issues like patient recruitment shortfalls or data discrepancies. Success in this role requires strong organizational skills, adaptability, and proactive problem-solving to keep studies on track and compliant.

How much does a clinical trial manager earn?

A clinical trial manager's salary varies based on experience, location, and the size of the organization, but typically ranges from $80,000 to $130,000 annually. Senior managers or those with specialized skills and certifications can earn higher salaries, often exceeding $150,000. The role often requires knowledge of regulatory requirements and project management tools.

What qualifications do you need to be a clinical trial manager?

A clinical trial manager typically needs a bachelor's degree in life sciences, healthcare, or a related field, along with experience in clinical research or project management. Many roles also require knowledge of Good Clinical Practice (GCP) guidelines and proficiency with trial management software. Advanced degrees or certifications such as the Certified Clinical Research Professional (CCRP) can enhance job prospects.
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Clinical Trial Manager jobs near you
Infographic showing various Clinical Trial Manager job openings in Boca Raton, FL as of August 2026, with employment types broken down into 85% Full Time, 14% Part Time, and 1% Contract. Highlights an 81% Physical, 2% Hybrid, and 17% Remote job distribution, with an average salary of $123,398 per year, or $59.3 per hour.

Clinical Research Coordinator

DERMCARE MANAGEMENT LLC

Hollywood, FL • On-site

$22.25 - $29.50/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 10 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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