Onsite Associate Director, Physician – CVRM

Posted 3 hours ago

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About the role

  • 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

Job title

Associate Director, Physician – CVRM

Job type

Experience level

Senior

Salary

Not specified

Degree requirement

Postgraduate Degree

Location requirements

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