JOB DESCRIPTION
Work Schedule
Standard (Mon-Fri)Environmental Conditions
OfficeJob Description
Join us as a Research Associate – And assist in the coordination of clinical trials, manage data and sample collection, support site activities, ensure protocol compliance, and contribute to the advancement of our research projects.
At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future. What You’ll Do:• Perform non-technical procedures, including urine collection, subject walks and safety monitoring.
• Under the general supervision of a licensed physician, may conduct the education, evaluation, patient treatment and follow-up
• Support the front desk tasks such as patient check-in, scheduling, reminder calls, & chart building
• Prepare and calibrate equipment for testing to ensure proper functioning.
• Interact regularly with patients during study visits in order to perform study related procedures.
• Undertake screening tests in accordance with protocol requirements.
• Answer incoming telephone calls.
• Assist in the lab and/or liaises with laboratories regarding sample collections and sample processing.
• Complete clinical supply orders and maintains appropriate levels.
• May collect medical history information for potential patients, liaising with medical facilities and networks to collect patient files, documentation and other relevant information as may be required as per protocol.
• Maintain accurate freezer logs, specimen labelling and other documentation when required.
• May take consent if permitted according to country regulation.
• Report Quality Incidents and supports investigation and resolution.
• Provide administrative support as needed.
• Ensure adherence to COP’s, SOP’s and GCP and local regulations.
Compensation and Benefits
The hourly pay range estimated for this position based in Minnesota is $19.00–$22.00.This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:
A choice of national medical and dental plans, and a national vision plan, including health incentive programs
Employee assistance and family support programs, including commuter benefits and tuition reimbursement
At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount
For more information on our benefits, please visit:
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