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Clinical Research Coordinator

0-2 years
Not Disclosed
10 Nov. 13, 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

Location: Richfield, Minnesota, United States
Job ID: R-01331478
Job Type: Full-Time
Category: Clinical Research
Work Mode: Fully Onsite


About the Company

At Thermo Fisher Scientific, you’ll be part of a global mission — enabling customers to make the world healthier, cleaner, and safer.
Through our PPD® clinical research portfolio, we conduct trials across 100+ countries, integrating laboratory, digital, and decentralized clinical trial services. Our teams are committed to advancing life-changing therapies with precision and care.


Work Schedule

  • Shift: First Shift (Days)

  • Work Environment: Office-based, fully onsite


About the Department – Medical Communications

Within Medical Communications, we support patient health by providing accurate medical information services to customers, healthcare providers, and regulatory agencies.
Key focus areas include:

  • Managing medical inquiries, adverse event reports, and product complaints

  • Supporting product launches

  • Developing process improvements

  • Ensuring compliance with global regulatory standards


Role Overview – Clinical Research Coordinator

As a Clinical Research Coordinator (CRC), you will work under the direction of the Chief Physician/Investigator and Staff Paramedic to ensure subject safety, data integrity, and protocol compliance throughout the study.
You will assist in conducting clinical studies according to FDA, ICH-GCP, and company procedures, while directly engaging with patients and supporting all operational aspects of clinical trials.


Key Responsibilities

  • Conduct clinical trials in compliance with FDA/GCP/ICH regulations.

  • Provide medical care and ensure patient safety at all times.

  • Perform study activities such as:

    • Informed consent

    • Screening

    • Vital signs, ECGs, pregnancy tests, height, and weight measurements

  • Record and verify patient data on required forms and electronic systems (EDC/CRF).

  • Maintain IP (Investigational Product) accountability logs as required.

  • Report non-compliance to site management and ensure IRB requirements are met.

  • Build strong relationships with patients to support retention and compliance.

  • Attend site initiation and training meetings for study-specific guidance.

  • Manage patient scheduling, follow-up calls, and result communication.

  • Ensure accuracy and timeliness in all data entries and sponsor communications.

  • Maintain and update source documents and patient files.

  • Adhere to company COP/SCOP (Controlled Operating Procedures).

  • Support general clinic hygiene, including proper waste disposal and workspace upkeep.


Qualifications

Education

  • Bachelor’s degree (or equivalent vocational qualification) in Clinical, Life Science, or Medical field

Certifications

  • BLS (Basic Life Support) certification required

Experience

  • 0–2 years of relevant clinical or research experience

  • Knowledge of GCP, FDA, and ICH standards preferred


Skills & Competencies

  • Strong attention to detail and organizational skills

  • Excellent written and verbal communication

  • Ability to collaborate with investigators, coordinators, and research teams

  • Commitment to maintaining high standards of data integrity and patient care


Compensation & Benefits

Compensation

  • Position: Clinical Research Coordinator I

  • Location-based Pay Range: (To be determined based on Minnesota rates)

  • Bonus Eligibility: Annual performance-based variable bonus

Total Rewards Package Includes:

  • Medical, dental, and vision plans (national coverage)

  • Health incentive programs

  • Employee assistance and family support programs

  • Commuter benefits and tuition reimbursement

  • Paid Time Off (PTO): At least 120 hours annually

  • Paid Holidays: 10 per year

  • Paid Parental Leave: 3 weeks bonding + 8 weeks caregiver leave

  • Insurance: Accident, life, short- and long-term disability

  • Retirement: Competitive 401(k) savings plan

  • Employee Stock Purchase Plan (ESPP) – discounted company stock options

🔗 More Information: Thermo Fisher Total Rewards


Equal Opportunity Statement

Thermo Fisher Scientific is an Equal Opportunity Employer.
All qualified applicants will receive consideration for employment without discrimination based on race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.