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Clinical Research Technician I, Early Phase Clinical Research

Fortrea
0-1 years
Not Disclosed
Daytona Beach, United States
1 June 9, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: ICSR Case Processing, Interpersonal Skill, Labelling Assessment

Clinical Research Technician I – Early Phase Clinical Research

Location: Daytona Beach, Florida
Job Type: Full-Time, On-Site
Job Requisition ID: 262578


About the Role

We are seeking a detail-oriented and motivated Clinical Research Technician I to support Early Phase Clinical Research studies at our Daytona Beach, FL facility. This role is ideal for individuals with clinical experience in phlebotomy, vital signs collection, and patient-facing healthcare environments who are interested in contributing to the development of innovative therapies.

As part of a leading global Clinical Research Organization (CRO), you will work directly with research participants and clinical teams to ensure study procedures are performed accurately, safely, and in compliance with protocol and regulatory requirements.

Required Skills: Phlebotomy, Vital Signs Collection, and Exceptional Attention to Detail.


Key Responsibilities

Clinical Trial Procedures

  • Perform clinical and administrative study activities according to study protocols and regulatory requirements.

  • Collect and accurately document participant data and clinical assessments.

  • Ensure compliance with study procedures, safety requirements, and Good Clinical Practice (GCP) standards.

Participant Assessments

  • Accurately perform and document:

    • Blood Pressure Measurements

    • Pulse Rate

    • Respiratory Rate

    • Body Temperature

    • Weight Measurements

  • Monitor participant well-being throughout study procedures.

Phlebotomy & Sample Collection

  • Perform venipuncture and blood collection procedures.

  • Collect, process, label, and prepare biological samples according to protocol requirements.

  • Ensure proper handling, storage, and distribution of samples.

ECG & Clinical Monitoring

  • Prepare and accurately record:

    • Electrocardiograms (ECGs)

    • Holter Monitor Assessments

  • Maintain high standards of data accuracy and documentation.

Participant Support

  • Monitor participant meals to ensure dietary compliance with study requirements.

  • Assist participants during study visits and procedures.

  • Support participant screening activities when required.

Clinical Operations Support

  • Prepare examination rooms and clinical areas.

  • Set up and maintain medical equipment required for study procedures.

  • Assist with operational activities to ensure efficient study execution.

  • Perform additional duties as assigned by management.


Required Qualifications

Education

  • High School Diploma or equivalent required.

Equivalent relevant experience may be considered in place of formal educational requirements.

Experience

  • 0–1 year of clinical research experience preferred.

  • Previous clinical or healthcare experience is highly desirable.

  • Recent graduates with relevant clinical exposure are encouraged to apply.

Certifications

  • Current CPR/AED Certification required.

Required Skills

  • Phlebotomy and venipuncture experience.

  • Experience taking and recording vital signs.

  • Strong attention to detail and documentation accuracy.

  • Basic computer and data entry skills.

  • Excellent communication and interpersonal skills.

  • Ability to work effectively within a team environment.