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Clinical Research Technician - Daytona Beach, Fl (On-Site)

Fortrea
Fortrea
1 years
Not Disclosed
Daytona Beach, Florida, United States
10 Feb. 24, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Clinical Research Technician – Early Phase Clinical Trials (On-Site)

Location: Daytona Beach, Florida, United States
Category: Clinical Operations
Job ID: 26273
Employment Type: Full-Time (Rotating Shifts, Including Some Weekends)
Experience Required: Minimum 1 Year Related Clinical Experience

About the Company

Fortrea is a leading global contract research organization (CRO) with extensive experience in clinical development across more than 20 therapeutic areas. Operating in over 90 countries, Fortrea partners with pharmaceutical, biotechnology, and medical device companies to accelerate drug and device development through scientific rigor and operational excellence.

Role Overview

The Clinical Research Technician will support early-phase clinical trials by working directly with healthy volunteer participants in a structured, protocol-driven clinical research unit in Daytona Beach, FL. This role is ideal for Certified Nursing Assistants (CNA), Medical Assistants (CMA), EMTs, or healthcare technicians seeking to transition into clinical research operations.

The position involves rotating shifts, including some weekends, within an on-site clinical environment.

Key Responsibilities

Clinical Procedures & Participant Monitoring

  • Accurately measure and document blood pressure, pulse, respiratory rate, temperature, and body weight

  • Perform venipuncture and ensure proper sample labeling and handling

  • Prepare and record ECG and Holter monitoring procedures

  • Monitor participant dietary compliance according to protocol

Sample Collection & Processing

  • Collect, process, and distribute biological samples per study protocol

  • Maintain accurate source documentation and regulatory-compliant records

Operational Support

  • Prepare clinical rooms and medical equipment for study visits

  • Assist with screening procedures and participant flow

  • Maintain a clean, safe, and efficient clinical and laboratory environment

  • Support electronic data collection and documentation systems

Educational Qualifications & Experience Requirements

  • High School Diploma or equivalent required

  • Minimum 1 year of related healthcare or clinical experience required

  • Phlebotomy experience mandatory

  • EMT, CMA, or CNA certification preferred

  • Equivalent relevant experience may be considered

Work Environment

  • On-site laboratory and clinical research setting in Daytona Beach, FL

  • Exposure to biological fluids

  • Use of personal protective equipment (PPE) including gloves and protective garments

  • Occasional local travel and limited domestic travel may be required

Physical Requirements

  • Ability to stand or remain upright for 6–8 hours per shift

  • Repetitive hand movements for clinical and laboratory procedures

  • Occasional bending, crouching, and lifting up to 15–20 lbs

  • Proficiency with clinical software and electronic data systems

Core Competencies

  • Strong attention to detail and adherence to clinical trial protocols

  • Ability to perform in fast-paced, compliance-driven environments

  • Strong teamwork and interpersonal communication skills

  • Adaptability to changing study priorities

  • Comfort with technology-based clinical documentation systems

Compensation & Benefits

Eligible employees working 20+ hours per week may receive:

  • Medical, Dental, Vision, Life Insurance, STD/LTD

  • 401(k) Retirement Plan

  • Paid Time Off (PTO)

  • Employee Recognition Programs

  • Employee Resource Groups (ERGs)

Why Consider This Opportunity?

This position offers hands-on exposure to early-phase clinical research, allowing healthcare professionals to contribute to first-in-human and safety-focused studies that shape future therapeutic advancements.

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