Apply

Ready to go for it?

AI Apply speeds things up—apply directly if you prefer.

FREE ACCESS
5,000–10,000 jobs/day
JobTailor Logo

See all jobs on JobTailor

Search thousands of fresh jobs every day.

Discover
  • Fresh listings
  • Fast filters
  • No subscription required
Create a free account and start exploring right away.
Thermo Fisher Scientific

Traveling Clinical Research Coordinator II

Thermo Fisher Scientific

Traveling Clinical Research Coordinator II at Thermo Fisher Scientific overseeing clinical site activities. Conducting studies and ensuring patient safety and data integrity in a hybrid work environment.

Posted 5/20/2026full-timeFlorida, Illinois, Minnesota, Texas • 🇺🇸 United StatesJuniorMid-Level💰 $80,000 - $105,000 per yearWebsite

Tech Stack

Tools & technologies
Google Cloud Platform

About the role

Key responsibilities & impact
  • Conduct clinical studies according to FDA/GCP and ICH regulations and guidelines.
  • Provide medical care to patients, always ensuring patient safety comes first.
  • Schedule subject visits within protocol windows, ensuring scheduling capacity is maximized.
  • Perform all defined study activities (i.e., informed consent, screening, and protocol procedures which include but are not limited to vital signs, pregnancy tests, height, weight, ECG's, etc.).
  • Record all patient information and results from tests as per protocol on required forms.
  • Where required, may complete IP accountability logs and associated information.
  • Reports suspected non-compliance with relevant site staff.
  • Ensures that IRB approval is obtained prior to study initiation and IRB requirements are met throughout the study.
  • Promotes the company and builds a positive relationship with patients to ensure retention.
  • Attend site initiation meetings and all other relevant meetings to receive training on protocol.
  • May be required to call patients, do patient bookings and follow-up calls to confirm bookings or provide information or results.
  • Logs/complete information on sponsor systems and ensures all information provided is accurate (i.e., case report forms, EDC, etc.) and ensures it is completed within timeframe.
  • Gather and maintain source documents, updates patient files and notes, always ensuring relevant and most up to date information is recorded.
  • Adhere to company COP/SCOP.
  • May be required to dispose of waste according to standards and assist in keeping a general neat appearance of the facility.

Requirements

What you’ll need
  • Bachelor's degree or equivalent and relevant formal academic / vocational qualification
  • BLS certificate preferred. GCP knowledge: certificate can be earned once hired, CRC Certification preferred but not required.
  • Previous experience to provide the knowledge, skills, and abilities to perform the job (comparable to 2+ years’).
  • Solid understanding of the clinical research process (i.e., GCP, SOPs, informed consent, safety monitoring, etc.)
  • Capable of working independently, analyzing and working with attention to detail, processing and prioritizing sensitive complex information and problem solving
  • Demonstrated ability to exercise discretion and sound judgement
  • Good decision-making, negotiation and influencing skills
  • Good communication skills and English fluency will be an advantage
  • Good organizational skills
  • Good proficiency in basic computer applications
  • Good interpersonal skills to work in a team environment

Benefits

Comp & perks
  • 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
  • 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

ATS Keywords

✓ Tailor your resume
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools
clinical studiesFDA regulationsGCPICH regulationsinformed consentsafety monitoringvital signsECGcase report formsEDC
Soft Skills
attention to detailproblem solvingdiscretionjudgementdecision-makingnegotiationinfluencingcommunicationorganizational skillsinterpersonal skills
Certifications
Bachelor's degreeBLS certificateGCP knowledgeCRC Certification