长沙招聘

? Acts as a Regulatory Team Leader on more complex projects, which may include technical writing.

? Prepares and/or reviews regulatory documentation in area of expertise, as appropriate.

? Establishes relationships with many customers; may meet face to face without rest of the team to discuss regulatory issues, present lessons learned and discuss customer comments.

? Understands the Scope of Work, deliverables and management of budget for any given project and manages workload as appropriate.

? May give guidance to junior colleagues, including feedback on the quality of technical documents, and may assist in their training and development.

? May present to clients on complex regulatory processes at large full service bid defence meetings by phone or in person.

? May act as reviewer for regulatory SOPs, as assigned and appropriate.

? May prepare and deliver regulatory training to Quintiles small groups or individuals.

? Performs other tasks or assignments, as delegated by Regulatory management.

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.