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Screening Technician / Dallas, Tx (On-Site)

Fortrea
Fortrea
2+ years
Not Disclosed
Dallas, United States
10 April 22, 2026
Job Description
Job Type: Full Time Education: B.Pharm. or Post-Graduation (Microbiology/Quality Assurance/Biochemistry/Biotechnology) 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

Job Title:

Screening Technician (Clinical Research Unit)


Location:

Dallas, Texas, USA


Job Type:

Full-Time (Clinic/Office-Based)


Work Schedule:

  • Monday to Friday: 7:00 AM – 3:30 PM
  • Occasional early start or extended hours based on study requirements

Job Overview:

The Screening Technician supports early-phase clinical trials (Phase I) by interacting directly with healthy volunteers and performing clinical procedures. This role involves patient care, sample collection, data recording, and protocol compliance, ensuring high standards of safety, accuracy, and efficiency in a fast-paced clinical research environment.


Key Responsibilities:

Clinical Procedures:

  • Measure and record vital signs:
    • Blood pressure
    • Pulse
    • Respiratory rate
    • Temperature
    • Weight
  • Perform venipuncture (phlebotomy)
  • Prepare and record ECGs/Holter monitoring
  • Collect and process biological samples as per protocol

Participant Care & Monitoring:

  • Monitor participants for well-being and safety
  • Ensure dietary compliance during study participation
  • Handle participant check-in and check-out
  • Address participant concerns and complaints professionally
  • Maintain participant dignity, safety, and confidentiality

Study Support Activities:

  • Assist with screening procedures and study tasks
  • Prepare rooms and clinical equipment
  • Maintain a clean and safe study environment
  • Assist with quality control (QC) of documents and case report forms
  • Support study procedures as required

Data Management & Documentation:

  • Accurately record all clinical and research data
  • Maintain proper documentation as per protocol
  • Ensure timely response to team and client queries
  • Maintain awareness of regulatory requirements

Team & Operational Support:

  • Participate in required meetings
  • Collaborate effectively with team members
  • Adapt to changing priorities in a fast-paced environment
  • Take ownership of work quality and compliance

Qualifications (Minimum Required):

  • High School Diploma or equivalent

Certifications (Preferred):

  • EMT (Emergency Medical Technician)
  • Phlebotomy Certification
  • CMA (Certified Medical Assistant)
  • CNA (Certified Nursing Assistant)

Experience Requirements:

  • Mandatory:
    • Experience as a Medical Technician / Screening Technician / Nursing Assistant
    • Phlebotomy (venipuncture) experience
  • Preferred:
    • Prior clinical research experience

Skills & Competencies:

  • Strong clinical and patient care skills
  • Attention to detail and accuracy
  • Ability to follow strict study protocols
  • Strong teamwork and communication skills
  • Adaptability in a dynamic environment
  • Basic knowledge of regulatory and clinical research practices
  • Comfort with electronic data capture systems

Work Environment:

  • Fast-paced clinical research setting
  • Protocol-driven environment with strict timelines
  • Technology-based data collection systems

Compensation & Benefits:

Eligible employees (20+ hours/week) receive:

  • Medical, Dental, Vision Insurance
  • Life Insurance, STD/LTD
  • 401(K) Plan
  • Paid Time Off (PTO)
  • Employee Recognition Programs
  • Employee Resource Groups (ERGs)

Physical Requirements:

  • Ability to stand or sit for 6–8 hours/day
  • Repetitive hand movements for operating lab equipment
  • Frequent bending, twisting, and occasional crouching
  • Ability to lift 15–20 lbs
  • Regular and consistent attendance required
  • Flexible working hours as needed

Additional Information:

  • Exposure to early-phase clinical trials (e.g., first-in-human, dose escalation, drug interaction studies)
  • Opportunity to work with leading pharmaceutical and biotech companies
  • Direct involvement in the development of new medical treatments