Associate Director, Physician managing clinical trials in the pharma industry. Leading project execution and providing expertise in CVRM therapeutic areas.
Responsibilities
Provides expertise to China development strategy and plan for all portfolio projects within the own area of specialty.
Leads and/or performs China protocol development, preparation for clinical challenges and governance committee review, as well as health authority interactions.
Manages clinical trials as a medical lead to deliver study with cooperating with cross-functional partners.
Provides, as an expert, strategic physician expertise to quantify the benefits, risks, value and uncertainty of clinical trials.
Ensures efficient and effective leadership and management of project information, strategy, quality standards, and integrity of information interpretation.
Networks with colleagues and experts, providing medical consultancy in own area of expertise and serving as a resource for others by sharing experience within and beyond project team.
Keeps close connection with global study team during the entire course of the study.
Coaches junior physicians and provides supervision as needed.
Keeps own knowledge of best practices and new relevant developments up to date
Requirements
Master degree in Clinical Medicine or M.D. or Ph.D.
Experience as a clinical physician
Experience of management and design of clinical trials
Minimum 7 years of experience as clinical research physician in pharma industry R&D
Therapeutic area expertise in CVRM.
Benefits
AstraZeneca embraces diversity and equality of opportunity
Committed to building an inclusive and diverse team
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