Global Clinical Study Specialist

ICON Strategic SolutionsWarren, NJ, US

4 hours ago

Job type

Full-time

Permanent

Job description

Job Description

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

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Clinical Study Specialist • Warren, NJ, US