ICON just opened a Global Clinical Study Specialist position, and I wanted to see if you know anyone that might be interested.
Must be open to hybrid office/home based in Warren NJ or Armonk NY - 3 days per week in office with the other 2 days remote.
Full time, direct hire, full benefits with salary up to $85,000 (No bonus)
2 years of related industry experience including at a Pharmaceutical or Biotechnology company: eTMF, supporting global trials, Oncology or Hematology experience.
Meeting Minutes and action items • Tracker management (list possible trackers) • Site communications • CRO communications/oversight • TMF responsibilities: IRR, EDL, uploading documents • ICF updates • Protocol Deviation Review meeting • feasibility---- Must understand the protocols, understand protocol deviation.
Global studies experience• Processes Veeva Vault / Medidata RAVE EDC / Sharepoint / ODR Operational Data Repository reports / MyQumas / AIR Tracker (Excel) / QMOD (CRC review, SSN Reporting) / Oracle / MS Teams-- experience in vendor interaction and oversight preferred
Clinical Study Specialist position
You are:
Must have a Bachelor's Degree
Required qualifications
Ideal Answer: Yes
Ideal Answer: Yes
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