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Clinical Research Coordinator I

0-2 years
Not Disclosed
10 June 3, 2025
Job Description
Job Type: Remote Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science 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

 

Job Title:

Clinical Research Coordinator I


Location:

Evansville, Indiana, United States
Job ID: R-01303654
Job Type: Full-time
Remote Status: Fully Onsite
Work Schedule: Standard (Mon–Fri)


Company Overview:

At Thermo Fisher Scientific, through our PPD® clinical research portfolio and Accelerated Enrollment Solutions (AES), we lead the way in advancing medical science by optimizing every step of the clinical trial journey. With global reach and local impact, we empower professionals to drive innovation that improves lives.


Position Summary:

As a Clinical Research Coordinator I, you will support clinical trials from start to finish, ensuring that studies are conducted in compliance with FDA, ICH/GCP regulations, and internal protocols. You’ll perform medical procedures, manage patient data, and collaborate across study teams to improve the development of novel therapies.


Key Responsibilities:

Study Execution:

  • Conduct study activities including informed consent, screenings, vital signs, ECGs, and more.

  • Ensure compliance with clinical protocols and regulatory guidelines.

  • Maintain accurate and complete source documentation and case report forms (CRFs).

  • Log data in sponsor systems such as EDC (electronic data capture) platforms.

  • Monitor subject safety and report non-compliance or adverse events.

  • Attend study meetings and trainings, including site initiation visits.

Participant Support:

  • Provide direct patient care during trials.

  • Maintain ongoing communication and positive rapport with study participants to ensure retention and satisfaction.

  • Schedule and follow up on patient appointments as needed.

Site Coordination:

  • Ensure IRB approvals and documentation are current and compliant.

  • Maintain clinical and patient files accurately.

  • Collaborate closely with the site and sponsor teams to meet enrollment and study timelines.


Qualifications:

Education:

  • Bachelor’s degree or equivalent vocational qualification in the clinical or medical field required.

Experience:

  • 0–2 years of relevant experience in clinical research or a healthcare setting.

  • Equivalent combinations of education and experience will be considered.


Knowledge, Skills, and Abilities:

  • Basic understanding of clinical trial processes (GCP, SOPs, informed consent, safety monitoring).

  • Excellent attention to detail and organizational skills.

  • Strong verbal and written communication skills.

  • Proficient in basic computer systems and Microsoft Office.

  • Ability to work independently and manage priorities under pressure.

  • Collaborative mindset with strong interpersonal skills.


Physical & Work Environment Requirements:

  • Exposure to biological fluids and clinical environments.

  • Must wear PPE including gloves, garments, and eyewear.

  • Ability to lift 15–20 lbs and sit or stand for extended periods.

  • Frequent bending, twisting, and mobility required.

  • Some domestic or international travel may be needed.


Benefits:

  • Competitive salary and annual incentive plan.

  • Comprehensive health, dental, vision insurance.

  • Paid time off (PTO), holidays, and parental leave.

  • Tuition reimbursement, 401(k) with company match, and stock purchase plan.

  • Career growth and development in a mission-driven, global organization.