长沙招聘

Responsibilities

Essential Functions

? Review and negotiate site regulatory documents and contracts with sites and sponsors for agreement on wording and

budgets.

? Maintain and manage SSU data tracking entries in database. Review for completeness and accuracy.

? Review and provide feedback to management on site performance metrics.

? Serve as contact for investigative sites, designated project reports, communications, and customer service.

? Resolve site issues and determine status for product shipment.

? Work with regulatory team members or sponsor to secure authorization of regulatory documents.

? Work with legal team members or sponsor to secure authorization of contracts.

? Work with Clinical Operations, Project Management and Site Identification on SSU project specific status and deliverables.

? Inform team members of completion of regulatory and contractual documents for individual sites.

? Work with team members in preparation of regulatory submissions per work instructions.

? May serve as a SSU Team Lead for country or region as needed. Coordinate activities for projects within area of

specialization.

? May translate or review completed translations of critical documents.

? May participate in feasibility and/or site identification activities.

QuintilesIMS pioneered the idea of helping pharma companies conduct objective clinical trials to establish not only whether a drug is effective, but who can take it safely. Our customers have relied on us to design and conduct rigorous clinical research for decades, from small studies to multinational mega-trials. However, we continue to develop new ways of interpreting and evaluating data that allow us to create more effective trials and determine outcomes faster.
 
If that is your passion, we have a place for you.