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Research Technician, Early Phase Clinical Research - Dallas, Tx

Fortrea
Fortrea
1 years
Not Disclosed
Dallas, United States
10 March 3, 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

Research Technician, Early Phase Clinical Research – Full-Time | Dallas, Texas, USA

Location: Dallas, Texas, United States
Job Type: Full-Time (Rotating Shifts, Including Some Weekends)
Department: Early Phase Clinical Research
Experience Required: Minimum 1 year of related clinical or healthcare experience (Phlebotomy experience required)

Company Overview

Fortrea is a leading global Contract Research Organization (CRO) delivering clinical development, patient access, and technology solutions across more than 20 therapeutic areas. With operations spanning over 90 countries and a workforce of 19,000+ professionals, the organization partners with pharmaceutical, biotechnology, and medical device companies to accelerate drug and device development worldwide.

Job Overview

We are hiring a Research Technician to support early phase clinical trials in a fast-paced, protocol-driven research environment. This position is ideal for Certified Nursing Assistants (CNA), Medical Assistants (CMA), Emergency Medical Technicians (EMT), or healthcare professionals seeking to transition into clinical research.

The Research Technician will interact directly with healthy volunteer participants, perform clinical procedures, collect biological samples, and ensure strict adherence to study protocols and regulatory requirements. This is an on-site role based in Dallas, TX, requiring rotating shifts and weekend availability.

Key Responsibilities

Clinical Procedures & Participant Care

  • Perform vital sign measurements including blood pressure, pulse, respiratory rate, temperature, and weight.

  • Conduct venipuncture and support phlebotomy procedures.

  • Prepare and accurately record ECGs and Holter monitoring data.

  • Assist with screening procedures in accordance with study protocols.

Sample Collection & Processing

  • Collect, process, label, and distribute biological samples as outlined in clinical study protocols.

  • Ensure accurate documentation and chain-of-custody compliance.

  • Monitor participant dietary compliance when required by protocol.

Operational Support

  • Prepare clinical rooms and medical equipment prior to study activities.

  • Maintain a clean, safe, and compliant clinical research environment.

  • Support electronic data capture processes in a technology-driven setting.

  • Assist with additional clinical and administrative tasks as assigned.

Required Qualifications

  • High School Diploma or equivalent.

  • Minimum 1 year of related healthcare or clinical experience.

  • Phlebotomy experience required.

  • Strong attention to detail and ability to follow strict study protocols.

Preferred Qualifications

  • EMT, CMA, or CNA certification.

  • Experience working in a laboratory, hospital, or clinical research environment.

  • Familiarity with electronic clinical documentation systems.

Work Environment & Physical Requirements

  • Office-based and clinical/laboratory environment.

  • Exposure to biological fluids; use of personal protective equipment required.

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

  • Frequent bending, twisting, and repetitive hand movements.

  • Light to moderate lifting up to 20 lbs.

  • Occasional local travel between site locations.

  • Rotating shifts and varied hours, including weekends.

Key Competencies

  • Ability to thrive in a highly regulated, fast-paced clinical trial setting.

  • Strong teamwork and communication skills.

  • Adaptability to changing priorities and strict timeline requirements.

  • Commitment to protocol compliance and participant safety.

  • Comfort working in an electronic data-driven environment.

Employee Benefits

Eligible full-time employees working 20+ hours per week may receive 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 Apply Through ThePharmaDaily

This opportunity is ideal for healthcare professionals transitioning into clinical research, early phase trials, phlebotomy-based roles, and CRO environments. If you are seeking hands-on clinical research experience in Dallas, TX with exposure to global drug development programs, apply now to advance your career in early phase clinical research operations.