1+ months

Associate Director, Clinician

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**Role** **Summary:**

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.

Posted: 2020-04-16 Expires: 2020-06-18
Sponsored by:
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