Associate Clinical Research Monitor – Short term Contract
at Medtronic
Milano, Lombardia, Italy -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 10 Jul, 2024 | Not Specified | 11 Apr, 2024 | 1 year(s) or above | Good communication skills | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
CAREERS THAT CHANGE LIVES
Relieving pain, restoring health, and prolonging life. It is driven by this mission that Medtronic continues to benefit millions of patients with its innovative therapies. Today you have the opportunity to join one of the largest medical device companies in the world and participate in this daily challenge. By joining our teams, you will be at the heart of our values!
As Associate Clinical Research Monitor you would be responsible for the oversight of clinical research conducted at investigational sites to ensure compliance with study protocols, applicable regulatory standards, Ethics Committee/Institutional Review Board (IRB/EC) policies as well as procedures and business policies. This position works under supervision as needed, with a lot of flexibility for personal development. You would work closely with study management teams within Medtronic and site personnel for resolution of site issues towards successful clinical studies execution.
Responsibilities:
Please refer the Job description for details
REQUIREMENT SUMMARY
Min:1.0Max:4.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Biology, Engineering
Proficient
1
Milano, Lombardia, Italy