Clinical Research Coordinator I
Location: Las Vegas, Nevada, USA
Job Type: Full-time
Work Schedule: Standard (Mon-Fri)
Work Setting: Fully onsite
Company: Thermo Fisher Scientific (PPD Clinical Research Portfolio)
The Clinical Research Coordinator I conducts ongoing clinical trials involving patients or healthy volunteers. The role ensures compliance with regulatory guidelines, facilitates study planning and execution, and supports positive interactions between patients and the research team from initiation to closeout.
Conduct clinical studies in adherence to FDA/GCP and ICH regulations, ensuring patient safety and medical care
Perform study activities including informed consent, screening, protocol procedures (vital signs, pregnancy tests, height, weight, ECGs)
Accurately record patient information, test results, and complete IP accountability logs
Report non-compliance and ensure IRB approval and adherence to study protocols
Promote the company and build positive relationships with patients
Manage patient bookings, follow-up calls, and log information in sponsor systems
Gather source documents, update patient files, and maintain a neat facility environment
Education:
Bachelor’s degree or equivalent experience in a clinical/medical field
BLS (Basic Life Support) certification required
Experience:
0–2 years of relevant clinical research experience, or equivalent combination of education, training, and directly relevant experience
Basic understanding of clinical research processes: GCP, SOPs, informed consent, safety monitoring
Ability to work autonomously, evaluate data, and prioritize detailed information
Strong decision-making, negotiation, and influencing skills
Excellent written and verbal communication skills in English
Strong organizational skills and attention to detail
Proficiency in basic computer applications
Ability to work effectively in a team environment
Work in office, laboratory, and clinical environments
Exposure to biological fluids and potential infectious organisms
Use of personal protective equipment (PPE) such as protective eyewear, garments, and gloves
Occasional domestic or international travel may be required
Ability to remain stationary for 6–8 hours daily
Repetitive hand movements, frequent mobility, occasional crouching, stooping, bending, and twisting
Ability to lift and carry objects up to 15–20 lbs
Perform tasks under stress and manage multiple priorities
Regular and consistent attendance required
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Siliguri |Illinois :
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Europe | France | Latvia | Lendava | Leuven | Poland | Slovenia | Spain |Finland :
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China | Quarry Bay |Liaoning :
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Arkansas | Remote Australia |New South Wales :
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Queensland |Melbourne :
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England | Harlow | Leeds | London | Maidenhead | Salt Lake City | Stevenage | Stirling | United Kingdom |North Yorkshire :
Harrogate |South Yorkshire :
Sheffield |Oxfordshire :
Witney |Ontario :
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Montreal |Brussels :
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Zaventem |South America :
Peru | Argentina |Brazil :
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Auckland |New Zealand :
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Tartu | Estonia |Harju County (Maakond) :
Tallinn |Hà Nội :
Hanoi | Hà Nội |Ho Chi Minh :
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