Instagram
youtube
Facebook

Clinical Research Coord I

0-2 years
Not Disclosed
10 Nov. 13, 2025
Job Description
Job Type: Full Time Remote 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, United States
🆔 Job ID: R-01332909
💼 Job Type: Full-Time | Category: Clinical Research
🏠 Work Setup: Fully Onsite | Schedule: Monday–Friday (Standard Hours)
🏢 Environment: Office / Clinical


Company Overview

At Thermo Fisher Scientific, you’ll contribute to work that makes a global impact — enabling our customers to make the world healthier, cleaner, and safer.
Through our PPD® clinical research portfolio, we conduct clinical trials in 100+ countries, advancing digital, decentralized, and traditional research models to deliver life-changing therapies worldwide.


Position Summary

The Clinical Research Coordinator I is responsible for conducting at least one ongoing clinical trial involving patients or healthy volunteers. The role involves coordinating study activities, maintaining patient safety, ensuring regulatory compliance, and supporting all phases of the clinical trial — from initiation to closeout.


Key Responsibilities

  • Conduct clinical studies in strict compliance with FDA, GCP, and ICH guidelines.

  • Obtain informed consent, perform patient screening, and execute protocol-specific procedures (e.g., vital signs, ECGs, pregnancy tests, height/weight measurements).

  • Accurately document patient data, test results, and maintain IP accountability logs.

  • Report deviations, non-compliance, and adverse events promptly.

  • Ensure IRB approvals are obtained and maintained.

  • Promote a positive image of the company through professional patient interaction.

  • Schedule and manage patient visits, follow-up calls, and maintain sponsor logs.

  • Compile and verify source documents and ensure data accuracy.

  • Maintain an organized and clean clinical environment in accordance with SOPs.


Qualifications

  • Education: Bachelor’s degree or equivalent in a clinical or medical field.

  • Certification: Basic Life Support (BLS) certificate (mandatory).

  • Experience: 0–2 years in a clinical research setting or equivalent combination of training and experience.


Skills & Competencies

  • Sound understanding of clinical research processes, including GCP, SOPs, informed consent, and patient safety monitoring.

  • Ability to analyze data, work independently, and prioritize multiple tasks with precision.

  • Excellent communication, organization, and interpersonal skills.

  • Decision-making, negotiation, and influencing abilities.

  • Proficiency in MS Office and other standard software tools.

  • Fluent in English (verbal and written).


Working Conditions

  • Work primarily in office, clinical, or laboratory settings.

  • Exposure to biological fluids, infectious organisms, and electrical office equipment.

  • Use of PPE (protective eyewear, gloves, garments) required.

  • Occasional domestic or international travel.


Physical Requirements

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

  • Frequent hand movements, bending, twisting, and mobility.

  • Occasional crouching or stooping.

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

  • Strong ability to communicate, multitask, and perform effectively under stress.

  • Regular and consistent attendance required.