Pfizer Associate Director, Clinician in Beijing, China
The China Clinician is responsible for high quality and timely delivery of one or
more interventional clinical trials for a Global Product Development /Global Established Pharma medicine.
They applytechnical excellence in the design of cost-efficient clinical trials to meet the needs
of internal and external customers, ensure effective conduct and medical/scientific
oversight of studies (in partnership with Development Operations) and support
appropriate interpretation and communication of clinical trial data (including high
quality regulatory submissions and product defense activities). They ensure
compliance with internal and external standards, proactively mitigate risk and
manage emerging clinical issues.
The China Clinician may act as a site liaison and point of contact to expedite study
start-up and conduct and to support clinical training, compliance and overall study
Depending on the program, the China Clinician may manage a group of 1 to 5
C h i n a Clinicians.
Required: M.D., Ph.D., D.V.M., M.S., and/or PharmD or equivalent qualifications.
Preferred: Postgraduate training/certification /fellowship in a medical discipline or in drug development. Demonstrated scientific productivity (e.g. doctoral thesis, publications, research reports, etc.) Experience
Required: Proven track record of being a successful Study Clinician (preferably in late phase development, or post-approval, as applicable to role).
Preferred: Thorough understanding of local / international regulations applicable to clinical trials (pre and post approval). Experience in pharmaceutical industry as people manager of clinical colleagues.
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.