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Clinical Research Coord I

0-2 years
Not Disclosed
10 Nov. 26, 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 ID: R-01332909
Employment Type: Full-Time
Work Model: Fully Onsite
Category: Clinical Research

Overview

Thermo Fisher Scientific’s Clinical Research team, supporting the PPD clinical research portfolio, plays a crucial role in advancing global healthcare solutions. Our teams contribute scientific and clinical expertise that accelerates the development of innovative therapies and brings life-changing treatments closer to patients.

In this role, you will support clinical trial operations from initiation through closeout, ensuring patient safety, regulatory compliance, and high-quality data collection.

Work Schedule

Standard (Monday to Friday)

Environmental Setting

Office and clinical environment


Position Summary

The Clinical Research Coordinator I is responsible for conducting at least one active clinical trial involving either patient participants or healthy volunteers. The role requires close coordination with site staff, patients, and interdepartmental teams to maintain study quality, compliance, and efficient workflow.


Key Responsibilities

Clinical Study Execution

  • Conduct clinical trial procedures in accordance with FDA, ICH, GCP, and protocol requirements.

  • Perform essential study activities, including informed consent, screening, and protocol-related assessments (vital signs, ECGs, pregnancy tests, height, weight).

  • Accurately document patient data, test results, and study logs, ensuring complete IP accountability.

  • Report any protocol deviations, safety concerns, or non-compliance.

  • Maintain IRB approvals and ensure site adherence to ethical and regulatory standards.

  • Support patient engagement, scheduling, follow-up calls, and interactions to ensure smooth trial participation.

  • Enter study-related information into sponsor systems and maintain updated patient files.

  • Preserve a professional and organized site environment.

Site and Patient Coordination

  • Promote a positive patient experience through consistent communication and support.

  • Collaborate with internal departments to ensure timely and accurate study deliverables.


Required Education and Experience

  • Bachelor’s degree in a clinical, medical, or health science field or equivalent relevant experience.

  • BLS (Basic Life Support) certification is mandatory.

  • Experience Required:

    • 0–2 years of prior clinical research or healthcare-related experience, demonstrating relevant skills and competencies.

    • A combination of education, training, and directly applicable experience may also be considered.


Skills and Competencies

  • Fundamental understanding of clinical research concepts, including GCP, SOPs, safety reporting, and informed consent.

  • Capability to work independently and manage multiple tasks with accuracy and attention to detail.

  • Strong analytical skills to evaluate data and prioritize activities.

  • Effective decision-making, negotiation, and problem-solving abilities.

  • Excellent written and verbal communication skills.

  • Proficiency in basic computer applications and ability to learn clinical research software tools.

  • Strong interpersonal skills to collaborate within multidisciplinary teams.

  • Well-developed organizational and time management abilities.


Working Conditions

  • Work conducted in office, laboratory, and clinical environments.

  • Possible exposure to biological materials and infectious agents.

  • Use of personal protective equipment (gloves, gowns, protective eyewear).

  • Exposure to standard office equipment.

  • Occasional domestic or international travel may be required.


Physical Requirements

  • Ability to remain seated or standing for 6–8 hours per day.

  • Frequent repetitive hand movements and routine physical activity.

  • Occasional stooping, crouching, bending, and twisting.

  • Ability to lift 15–20 lbs (luggage, equipment, laptop).

  • Strong verbal and written communication abilities.

  • Frequent interaction with diverse groups of individuals.

  • Ability to multitask and perform effectively under stress.

  • Consistent attendance is essential.