【ファイザー】[R&D] Clinical Development Medical, Associate Director, Research and Development - Vaccines
仕事内容
Role Summary
The clinician contributes towards providing medical and scientific expertise and oversight for Clinical Trials conducted worldwide with a primary focus in Japan and the Asia-Pacific region.
The clinician may be required to design a development strategy for multiple protocols designed to obtain approval particularly in Japan and other countries in Asia for a compound or group of compounds
Role Responsibilities
Protocol design and strategy:
Contributes towards the medical input during protocol development and updates to the clinical development plan.
Work closely with other clinicians and Japan study team members to ensure that documents (protocol, Informed Consent Document [ICD], etc.) meet regulatory requirements and company policy and has been reviewed by IRB/IECs.
Provides medical input into country feasibility.
応募資格(必須経験など)
Qualifications
Must have:
• Medical degree (M.D or equivalent).
• Licensed by a health authority to prescribe medicines (independent of supervision) for at least one year (post "intern/house officer" year) and has utilized the license to prescribe medicines in a patient care setting for an aggregate duration of at least one year.
• Possesses the ability to critically evaluate medical/scientific information.
• Excellent written and oral communication in English and Japanese.
• Understands the design, development, and execution of clinical programs and studies.
• Capacity to adapt to a fast paced and changing environment
Preferred/Nice to have:
• Documented work experience/knowledge of statistics
• Training and experience in infectious diseases and/or infection control in the hospital setting is preferred.
• Experience with investigational clinical trials is preferred.
• Flexibility to join frequent late night/early morning teleconferences with international study teams.
• Ability to travel domestically or internationally occasionally as required.