Vendor Management Specialist - Global Clinical Supplies
at Thermo Fisher Scientific
Home Office, Iowa, Czech -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 12 Feb, 2025 | Not Specified | 13 Nov, 2024 | 2 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:
JOB DESCRIPTION
Thermo Fisher Scientific Inc. is a world-class company that is dedicated to making a positive impact on a global scale. Our mission is to enable our customers to make the world healthier, cleaner, and safer. Join us in our pursuit of this ambitious goal and be part of a team that is committed to delivering exceptional results.
As a Vendor Management Specialist in our Global Clinical Supplies Team, you will play a crucial role in ensuring flawless execution of our clinical trials. You will have the opportunity to work with a diverse range of vendors and contribute to the development and delivery of life-changing therapies. Your expertise in vendor management will be instrumental in successfully implementing our clinical research projects.
Responsibilities:
- Oversight of contracting with vendors, including legal and contract modifications, where required.
- Set up strategy for the vendors to be involved to support clinical trials.
- Ensure all activities are carried out in accordance with company practices, client requirements, and GxP and SOPs.
- Provide financial management of vendor pass through costs.
- Ensure compliance with required guidelines to support assembling, packing and shipping of study medication or ancillary material. Provide on-going support to junior staff. May lead or manage day to day technician activities in absence of management.
- Proactively identify potential risks, create backup strategies, and effectively communicate with all parties involved.
- Oversight of inverse logistics processes, including returns, destruction, and recalibration activities.
- Participate in GCS mini team meetings, providing insight about vendors processes and procedures, costs, timelines, requirements, and deliverables.
- Participate in and support department project teams.
REQUIREMENT SUMMARY
Min:2.0Max:7.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Proficient
1
Home Office, Czech