Global Clinical Study Specialist (Pay increase)ICON Strategic Solutions • Armonk, NY, US
Global Clinical Study Specialist (Pay increase)
ICON Strategic Solutions • Armonk, NY, US
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job_description.job_card.job_descriptionProcesses 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 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 Have you completed the following level of education : Bachelor's Degree? Are you currently, or have you recently been, working at a Pharmaceutical, Biotechnology company or CRO as an FSP? 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?
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 $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
Clinical Study Specialist position
You are :
Must have a Bachelor's Degree
Required qualifications
Ideal Answer : Yes
Ideal Answer : Yes
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Clinical Study Specialist • Armonk, NY, US
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