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.
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