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Global Clinical Study Specialist

Global Clinical Study Specialist

ICON Strategic SolutionsArmonk, NY, US
1 day ago
Job type
  • Full-time
  • Permanent
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 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

  • 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

    • Required qualifications

  • Have you completed the following level of education : Bachelor's Degree?

    • Ideal Answer : Yes

  • Are you currently, or have you recently been, working at a Pharmaceutical, Biotechnology company or CRO as an FSP?

    • Ideal Answer : Yes

  • Do you have 2 years of clinical trial support experience including eTMF, supporting global trials, Oncology or Hematology experience at a Pharmaceutical, Biotechnology company or CRO through FSP?
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    Clinical Study Specialist • Armonk, NY, US

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