Instagram
youtube
Facebook

Clinical Research Coord I

0-2 years
Not Disclosed
10 Nov. 27, 2025
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ 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 (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.