Clinical Research Coordinator I (Onsite – Las Vegas, Nevada)
Job ID: R-01332909
Location: Las Vegas, Nevada, USA
Category: Clinical Research
Employment Type: Full-Time
Work Model: Fully Onsite
About the Role
Thermo Fisher Scientific is seeking a Clinical Research Coordinator I to support the planning, execution, and completion of clinical trials involving patients or healthy volunteers. This onsite role in Las Vegas requires close collaboration with research site teams and cross-functional departments to ensure high-quality clinical trial conduct aligned with global regulatory standards.
As part of the PPD® clinical research portfolio within Thermo Fisher Scientific, you will contribute to studies that accelerate the development of life-changing therapies worldwide.
Experience Level Required
Entry-Level to Early Career
0–2 years of experience in clinical research, healthcare, or a related medical field
Must have a Bachelor’s degree in a clinical/medical discipline or equivalent experience
BLS (Basic Life Support) certification required
Key Responsibilities
Clinical Trial Execution
Conduct clinical study activities in full compliance with FDA, GCP, ICH, and site SOPs.
Perform key protocol procedures including:
Informed consent
Patient screening
Vital signs
ECGs
Pregnancy testing
Height and weight measurements
Maintain accurate documentation of patient information, assessments, and test results.
Regulatory & Compliance
Ensure IRB approvals are obtained and maintained for relevant study protocols.
Complete investigational product (IP) accountability logs.
Identify, report, and document non-compliance issues promptly.
Maintain adherence to safety, ethical, and protocol standards.
Patient Coordination & Site Support
Manage patient scheduling, bookings, follow-up calls, and reminders.
Assist with maintaining patient files, source documents, and study records.
Promote the research site and foster strong patient engagement.
Operational & Administrative Duties
Enter patient and study-related data into sponsor systems.
Maintain clean, organized, and compliant clinical areas.
Support site teams from trial initiation to closeout.
Required Skills & Competencies
Foundational understanding of clinical research processes, GCP, informed consent, and safety reporting.
Ability to work independently with strong attention to detail.
Effective prioritization and data evaluation skills.
Strong communication skills with proficiency in English.
Good judgment, negotiation skills, and professional discretion.
Competency in basic computer applications (Word, Excel, email systems).
Strong interpersonal skills for cross-functional teamwork.
Working Conditions
Work conducted in office, laboratory, and clinical environments.
Exposure to biological samples and potential infectious agents.
Use of PPE such as gloves, protective eyewear, and lab garments is required.
Occasional domestic and international travel may be required.
Physical Requirements
Ability to remain seated or standing for 6–8 hours daily.
Frequent repetitive hand movements for data entry.
Regular mobility including bending, stooping, and twisting.
Ability to lift up to 15–20 lbs (e.g., equipment, laptops, carry-on bags).
Ability to communicate effectively with diverse patient and team populations.
Capacity to perform under stress and multitask effectively.
Consistent attendance is essential.
Why Join Thermo Fisher Scientific?
You will be part of a globally recognized organization dedicated to advancing human health through scientific innovation and high-quality clinical research. As part of the PPD® clinical research team, you will contribute to studies that improve clinical outcomes and support the development of transformative therapies.
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Siliguri |Illinois :
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Atlanta | Augusta | Rome |Maine :
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