Job Title: Clinical Research Technician – On-Site | Daytona Beach, Florida
Location: Daytona Beach, Florida, United States
Job Category: Clinical Research / Clinical Operations
Employment Type: Full-Time (Rotating Shifts, Including Some Weekends)
Experience Required: Minimum 1 year of related clinical or healthcare experience
Schedule: Rotating shift schedule provided in advance
About the Organization
Join Fortrea, a leading global Contract Research Organization (CRO) delivering comprehensive clinical development, patient access, and technology solutions across more than 20 therapeutic areas. With over 19,000 professionals operating in more than 90 countries, Fortrea partners with pharmaceutical, biotechnology, and medical device companies to accelerate drug and device development worldwide.
Fortrea is committed to scientific rigor, patient safety, and operational excellence in early and late-phase clinical research.
Position Overview
Fortrea is seeking a Clinical Research Technician to support on-site clinical trial operations in Daytona Beach, Florida. This role is ideal for Certified Nursing Assistants (CNA), Medical Assistants (MA), Emergency Medical Technicians (EMT), and allied healthcare professionals seeking to transition into clinical research.
As a Clinical Research Technician, you will work directly with healthy volunteer participants in a structured, protocol-driven research environment. You will assist in executing clinical study procedures while ensuring compliance with regulatory standards, data accuracy, and participant safety.
This is an office-based, laboratory and clinical unit position with rotating shifts, including some weekends.
Key Responsibilities
Interact directly with clinical trial participants in accordance with study protocols
Perform and accurately document vital signs, including blood pressure, pulse, respiratory rate, temperature, and weight
Conduct venipuncture and collect biological samples per protocol requirements
Process and distribute laboratory specimens in compliance with study guidelines
Prepare and record ECGs and Holter monitor readings
Monitor participant dietary compliance during study periods
Assist with screening procedures and clinical assessments
Prepare examination rooms and medical equipment for study visits
Maintain a clean, organized, and compliant clinical research environment
Enter and manage study data within electronic data capture systems
Perform additional duties as assigned to support clinical operations
Required Qualifications
High School Diploma or equivalent (relevant experience may be considered in lieu of formal education)
Minimum 1 year of related healthcare or clinical experience
Phlebotomy experience required
Strong attention to detail and adherence to protocol-driven procedures
Comfort working in a fast-paced, technology-based environment
Preferred Qualifications
EMT, CMA, or CNA certification
Prior exposure to clinical research or early-phase studies
Work Environment
Laboratory and clinical research unit setting
Exposure to biological fluids
Use of personal protective equipment (PPE), including protective eyewear, gloves, and garments
Occasional local driving to site locations and limited domestic travel
Use of electronic clinical systems and office equipment
Physical Requirements
Ability to stand or remain upright for 6–8 hours per shift
Repetitive hand and wrist movements for operating clinical and laboratory equipment
Frequent bending, twisting, and occasional stooping
Ability to lift and carry 15–20 lbs (including equipment and supplies)
Consistent and reliable attendance with flexibility for varied hours
Work Environment Expectations
Fast-paced, compliance-focused clinical research setting
Strict adherence to study protocols and timelines
Frequently shifting priorities requiring adaptability
Strong teamwork and communication skills
Fully electronic data collection systems
Compensation and Benefits
Employees working 20 or more hours per week are eligible for comprehensive benefits, including:
Medical, Dental, and Vision Insurance
Life Insurance and Short-Term/Long-Term Disability coverage
401(k) Retirement Plan
Paid Time Off (PTO)
Employee Recognition Programs
Employee Resource Groups (ERGs)
Why Join Fortrea
Fortrea fosters a collaborative and growth-oriented environment where healthcare professionals can expand their clinical expertise within the field of clinical research. By joining the Daytona Beach research team, you will contribute directly to the safe and efficient development of innovative therapies that impact patients globally.
Apply now through ThePharmaDaily.com to advance your career in clinical research and become part of a globally recognized CRO.
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