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Clinical Research Coord I

0-2 years
Not Disclosed
10 Nov. 14, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/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

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)


About the Role:

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.


Key Responsibilities:

  • 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


Qualifications:

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


Skills & Competencies:

  • 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 Environment / Physical Requirements:

  • 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