Job Title:
Clinical Research Coordinator
Location:
Richfield, Minnesota, United States
Job ID:
R-01331478
Job Type:
Full-Time
Category:
Clinical Research
Work Arrangement:
Fully Onsite
Work Schedule:
First Shift (Days)
Environment:
Office / Clinical Research Setting
About the Company
At Thermo Fisher Scientific, you’ll discover meaningful work that contributes to a healthier, cleaner, and safer world. Our Clinical Research Services team, powering the PPD® clinical research portfolio, operates across 100+ countries—leading advancements in laboratory, digital, and decentralized clinical trial solutions.
We are committed to supporting our colleagues with resources, training, and career growth opportunities while taking science beyond boundaries through research, development, and the delivery of life-changing therapies.
About the Role
The Clinical Research Coordinator plays a vital role in conducting clinical studies under FDA/GCP and ICH guidelines. Working under the direction of the Chief Physician/Investigator and Staff Paramedic, this role ensures participant safety, maintains study documentation, and supports protocol compliance throughout all phases of the study.
Key Responsibilities
Clinical & Technical Support
Conduct clinical studies following FDA, GCP, and ICH regulations.
Perform study-related activities, including informed consent, screening, and protocol-specific procedures (vital signs, ECGs, pregnancy tests, height, weight, etc.).
Provide medical care to study participants with patient safety as the top priority.
Observe, document, and manage Adverse Events (AEs), escalating to the physician/investigator when necessary.
Record all test results and patient data accurately in accordance with protocol requirements.
Regulatory & Compliance
Ensure IRB approval is obtained before study initiation and maintain compliance throughout the study.
Report any suspected protocol non-compliance to site management.
Complete Investigational Product (IP) accountability logs and documentation when required.
Adhere strictly to company COP/SCOP and regulatory documentation standards.
Patient & Site Management
Build and maintain positive relationships with study participants to encourage retention.
Attend site initiation meetings, trainings, and other study-related briefings.
Perform patient scheduling, follow-up calls, and provide updates on results or study information.
Maintain patient files and source documents, ensuring data accuracy and timely updates.
Assist with maintaining a clean, safe, and organized clinical environment, including proper waste disposal.
Documentation & Reporting
Log and complete information in sponsor systems (CRFs, EDC, etc.) accurately and within required timeframes.
Support preparation of reports, study documentation, and audit-ready materials as needed.
Qualifications
Education:
Bachelor’s degree or equivalent qualification in a clinical or medical field.
Experience:
0–2 years of relevant clinical or research experience.
Certifications:
Basic Life Support (BLS) certification required.
Skills & Attributes:
Strong understanding of clinical research regulations (FDA/GCP/ICH).
Excellent attention to detail and patient care focus.
Proficient in clinical documentation and data entry systems.
Effective verbal and written communication skills.
Team-oriented with the ability to work under physician supervision.
Compensation & Benefits
Thermo Fisher Scientific offers a comprehensive Total Rewards Package including:
Competitive hourly pay and annual performance-based bonus eligibility.
Choice of national medical, dental, and vision plans, including wellness incentives.
Employee assistance and family support programs, commuter benefits, and tuition reimbursement.
Paid Time Off (PTO): Minimum of 120 hours annually + 10 paid holidays.
Paid parental leave: 3 weeks bonding + 8 weeks caregiver leave.
Life, accident, and disability insurance per company policy.
401(k) retirement plan and Employee Stock Purchase Plan (ESPP) at a discounted rate.
👉 For detailed benefits information, visit:
https://jobs.thermofisher.com/global/en/total-rewards
Our Mission
To enable our customers to make the world healthier, cleaner, and safer.
Gujarat :
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Kannur | Kochi | Malappuram | Thiruvananthapuram | Trivandrum |Pondicherry (Puducherry) :
Pondicherry (Puducherry) |Jharkhand :
Ranchi |Sikkim :
Rangpo |India :
Siliguri |Illinois :
Abbott Park | Bloomingdale | Champaign | Chicago | Deerfield | Glenview | Lake Forest | Lombard | Naperville | Norridge | Park RIdge | Round Lake |Maryland :
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Appleton | Kenosha | Pleasant Prairie | Portage | Waukesha |United states :
Arizona | Buffalo Grove | Clayton | Downers Grove | fairmont | Georgia | Keene | Michigan | Mt. Pleasant | New Jersy | OH | Piedmont | Salisbury | United States | Whitesboro | Winston-Salem |Georgia :
Atlanta | Augusta | Rome |Maine :
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Frank Scottile Blvd |Missouri :
Fulton | Milan | St. Louis |United States :
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Hebron | Nebraska City |Hawaii :
Hilo | Honolulu |Tennessee :
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Mexico |northeastern :
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Bavaria |Bavaria :
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Frankfurt | Harveysburg |Germany :
Germany | GErmany |Lower Saxony :
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Hamburg |Rhineland Palatinate :
Ingelheim am Rhein | Mainz |Schleswig Holstein :
Kiel |Berlin :
Mitte |Mecklenburg Vorpommern :
Rostock |Saarland :
Saarbrucken |Switzerland :
Basel | Zurich |Serbia :
Belgrade | Serbia |Hungary :
Budapest |BULGARIA :
Bulgaria | Vedant |Denmark :
Copenhagen | Denmark |Europe :
Europe | France | Latvia | Lendava | Leuven | Poland | Slovenia | Spain |Finland :
Finland |Istanbul :
Istanbul | Turkey |Norway :
Norway | NOrway |Romania :
Romania |Belgium :
Wavre |Tipperary :
Ballydine |Cork :
Brinny | Ringaskiddy |Carlow :
Carlow |Republic of Ireland :
Cork | Dublin | Limerick | Waterford |Ulster :
Donegal |Meath :
Dunboyne |Dún Laoghaire :
Dún Laoghaire |Galway :
Galway |County Dublin :
Swords |Republic of China :
Beijing |China :
China | Quarry Bay |Liaoning :
Dalian |Zhejiang :
Hangzhou |Tokiyo :
Osaka | Tokyo |Shanghai Sai :
Shanghai Shi |Hubei :
Wuhan |Capital of Netherland :
Amsterdam |North Brabant :
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Haarlem |South Holland :
Leiden |Netherlands :
Netherlands |Remote Australia :
Arkansas | Remote Australia |New South Wales :
Ballina | Sydney |Republic of Western Australia :
Nedlands |Queensland :
Queensland |Melbourne :
South Yarra |United Kingdom :
England | Harlow | Leeds | London | Maidenhead | Salt Lake City | Stevenage | Stirling | United Kingdom |North Yorkshire :
Harrogate |South Yorkshire :
Sheffield |Oxfordshire :
Witney |Ontario :
Mississauga | North York | Australia | Uxbridge | Renfrew | Richmond Hill |Canada :
Canada |Quebec :
Montreal |Brussels :
Brussels |Antwerp :
Heist op den Berg |Flemish Brabant :
Zaventem |South America :
Argentina | Peru |Brazil :
Brazil | Sao paulo |Attica :
Athens | Koropi |Greece :
Greece |North Island :
Auckland |New Zealand :
New Zealand |Austria :
Austria |Vienna :
Vienna |Catalonia :
Barcelona |Madrid :
Madrid |Cebu Province :
Cebu City |Philippines :
Manila |Croatia :
Croatia |Zagreb :
Zagreb |Estonia :
Tartu | Estonia |Harju County (Maakond) :
Tallinn |Hà Nội :
Hanoi | Hà Nội |Ho Chi Minh :
Ho Chi Minh City |Italy :
Italy |Lombardy :
Rho |Jakarta :
Jakarta |East Java :
Surabaya |Japan :
Japan | Saitama |Tokyo :
Otemachi |North Ostrobothnia :
Oulu |Southwest Finland (Varsinais-Suomi) :
Turku |Remote Korea :
Remote Korea |Republic of Korea :
Seoul |Kazakhstan :
Almaty |Republic of Thailand :
Bangkok |Israel :
Yavne | Kfar Saba | Netanya | Be'Er Sheva | Tel Aviv |Remote :
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Bucharest |Buenos Aires :
Buenos Aires |Republic of Egypt :
Cairo |Mexico :
Ciudad de México | New Mexico |Dubai :
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King Abdullah Economic City | Khulais | Riyadh | Rabigh | Najran | Jeddah |Kuala Lumpur :
Kuala Lumpur |Kyiv Oblast :
Kyiv |Lima Region :
Lima |France :
Lyon | Paris |South Africa :
Midrand | South Africa |Nišava District :
Niš |Bohemia :
Prague |Chile :
Santiago |Bosnia and Herzegovina :
Sarajevo |Singapore :
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