Screening Technician – Clinical Research
Company: Clinical Research Organization (CRO)
Location: Madison, Wisconsin, USA
Job Type: Full-Time | On-Site
Work Schedule: Monday – Friday | 6:30 AM – 2:30 PM CST
Experience: 1 – 2 Years (Patient Care / Clinical Setting)
Qualification: Associate Degree or Bachelor’s Degree preferred
Approx Salary: $40,000 – $55,000 per year
Job Overview
The Screening Technician supports early-phase clinical trials by interacting directly with healthy volunteer participants and assisting in clinical screening procedures. The role involves performing clinical assessments, collecting biological samples, maintaining accurate records, and ensuring participant safety during Phase 1 clinical research studies. Candidates will work closely with research teams and gain exposure to various clinical trial types such as first-in-human, ascending dose, food effect, and drug-drug interaction studies.
Key Responsibilities
1. Clinical Screening & Participant Care
Perform vital signs monitoring, venipuncture, and ECG/Holter procedures.
Monitor participant health status and ensure compliance with study protocols.
Assist with participant check-in and check-out procedures.
Ensure participant safety, dignity, confidentiality, and overall well-being during clinical trials.
2. Sample Collection & Laboratory Support
Collect and process biological samples (blood, urine, etc.) according to study protocols.
Document sample collection and maintain accurate records.
Prepare clinical rooms and laboratory equipment for screening procedures.
3. Study Operations Support
Assist clinical research staff with study-related procedures.
Monitor dietary compliance and participant conditions during studies.
Maintain a clean and safe clinical research environment.
Support quality control documentation and study protocol compliance.
4. Data Management & Documentation
Record clinical data in electronic clinical systems.
Ensure documentation accuracy and adherence to research guidelines.
Respond promptly to inquiries related to participant care and study procedures.
Required Skills
Technical Skills
Vital signs monitoring and patient assessment
Venipuncture and phlebotomy procedures
ECG / Holter monitoring
Biological sample collection and processing
Basic knowledge of clinical research protocols and patient care procedures
Soft Skills
Strong attention to detail and protocol compliance
Good communication and interpersonal skills
Ability to work in fast-paced clinical research environments
Strong teamwork and adaptability
Preferred Qualifications
Certification as EMT, Phlebotomist, CMA, or CNA
Experience in clinical research or healthcare settings
Familiarity with electronic clinical data systems
Work Environment
Work performed in clinical and laboratory environments.
Exposure to biological samples and laboratory equipment.
Use of personal protective equipment (PPE) such as gloves, eyewear, and protective garments.
Occasional travel between research sites may be required.
Benefits
Medical, Dental, and Vision Insurance
Life Insurance and Disability Coverage
401(k) Retirement Plan
Paid Time Off (PTO)
Employee Recognition Programs
Employee Resource Groups and career development opportunities
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China | Quarry Bay |Liaoning :
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Canada |Quebec :
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Auckland |New Zealand :
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Madrid |Cebu Province :
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Croatia |Zagreb :
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Japan | Saitama |Tokyo :
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