Associate Medical Director

• Medical monitoring – answering day to day medical and scientific questions, provide daily medical support to Parexel staff or site

• Safety monitoring – Review and sign off adverse reports for accuracy and medical consistency, provide support for preparation of Periodic Safety Update Reports, review and sign off data listings for safety data, review adverse events and concomitant medications coding for accuracy and consistency.

• Provide medical expertise and training to Parexel personnel, sponsor, or site

• Provide medical support for the preparation of clinical protocols, final study report, statistical summary reports

• Provide medical input into pharmacovigilance workflows and projects, feasibility studies, Data Monitoring, Committees (DMCs), Clinical Endpoint Committees (CECs)

• Participate in proposal development teams for client bid defense meetings

QualificationsClinical practice experience at least 5 years

Endocrinology background

Solid background of internal medical is preferred

Good English skill in writing, listening and speaking

Industry experience or clinical trial experience is preferred

Good communication skill and team work capability & attitude

Good computer skill in office software