FSP Digital Provisioning Analyst
at Thermo Fisher Scientific
North Carolina, North Carolina, USA -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 31 Jan, 2025 | Not Specified | 01 Nov, 2024 | N/A | Global Health,It Support,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:
QUALIFICATIONS
- Experience with mobile device management platforms preferred.
- Proven experience in device provisioning or IT support, preferably in a clinical trial setting.
- Strong technical troubleshooting skills and the ability to compete in a fast-paced environment.
- Outstanding attention to detail and organizational skills.
- Excellent communication skills, both written and verbal.
- Ability to work collaboratively in a diverse and inclusive team environment.
Why Join Us?
At Thermo Fisher Scientific Inc., you will be part of an ambitious team that is making a tangible impact on global health. We offer an encouraging setting where your contributions are valued, and you can grow professionally while making a difference
Responsibilities:
ROLE OVERVIEW
Join a world-class team at Thermo Fisher Scientific Inc. as a Trial Supplies Associate I, where you can contribute to advancing clinical trials through outstanding IT support. This crucial role ensures flawless management of trial supplies, maintaining the highest standards of accuracy and efficiency.
KEY RESPONSIBILITIES
- Coordinate the setup, distribution, and management of mobile devices used in clinical trials.
- Ensure devices are configured strictly according to project-specific requirements.
- Provide devices to global end-users within determined timelines.
- Maintain accurate inventory reporting and additional project documentation as needed.
- Offer tier II technical support to internal helpdesk teams and end-users.
- Collaborate with cross-functional teams to successfully implement IT solutions that support clinical trials.
- Monitor and troubleshoot device issues to ensure flawless operation throughout the trial period.
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Information Technology/IT
Pharma / Biotech / Healthcare / Medical / R&D
Information Technology
Graduate
Proficient
1
North Carolina, USA