What are the responsibilities and job description for the Global Clinical Study Specialist position at ICON Strategic Solutions?
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 $75,000 (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 reveiw, SSN Reporting) / Oracle / MS Teams-- expereince in vendor interaction and oversight preferred
Clinical Study Specialist position
You are:
Must have a Bachelor's Degree
- Must have a minimum of 2 years industry related work experience
- Experience supporting global trials (NA, LAM, EU, APAC, India)
- Experience working in TMF, CTMS, Sharepoint,
- Excels in written and verbal communications
- Self-starter, can work independently with minimal oversight, solution-oriented
- ICF review experience
- General competency: powerpoint/excel skills, meeting minutes
- Vendor management/oversight experience a plus
- Must be open to hybrid office/home based in Warren NJ or Armonk NY
Salary : $75,000