AstraZeneca
Director Medical Affairs, CKD
AstraZeneca, Wilmington, Delaware, us, 19894
Introduction to role:Join AstraZeneca, a place where we turn ideas into life-changing medicines. As a Director Medical Affairs - CVRM, you’ll play a pivotal role in channeling our scientific capabilities to make a positive impact on changing patients’ lives. You will be a part of the CVRM Brand Core Medical Teams, responsible for the development and execution of the Brand Medical Plans.
Accountabilities:As a Director Medical Affairs, you will be accountable for the design and execution of the Medical Affairs components of the Dapagliflozin and Lokelma Medical Plans. Your responsibilities will include the development and delivery of appropriate scientific messaging and education to key customers and professional organizations; the development and execution of scientific and educational programs aligned with the Brand Medical Plan; delivery of medical and scientific insight back to the CVRM Brand Teams; and identification and targeting of key clinical investigators for key clinical trials.
Essential Skills/Experience:
Advanced degree (M.D., PhD, PharmD, MBBS) in a science-related field, such as Pharmacology, Pharmacy, Medicine, or equivalent
Over 5 years leading programs in a team environment
Validated understanding of medical strategy, clinical development, and medical science liaison areas
Ability to lead a diverse group of responsibilities
Ability to work efficiently in a cross-functional team environment
Authority technical depth in the disease area
Strategic influencing skills
Highly developed written and verbal communication skills
Well-developed initiative ability
Excellent project management skills
Strong organization and time management skills
Strong analytical and problem-solving skills
Preferred Skills/Experience:
Cardiovascular/Metabolic disease experience
Minimum 5 years experience in a strategy-setting role within Medical Affairs
Global experience within the pharmaceutical industry
Solid understanding of FDA requirements
Excellent digital literacy (Excel, Word, PowerPoint, etc.)
Knowledge of information/technology system
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Accountabilities:As a Director Medical Affairs, you will be accountable for the design and execution of the Medical Affairs components of the Dapagliflozin and Lokelma Medical Plans. Your responsibilities will include the development and delivery of appropriate scientific messaging and education to key customers and professional organizations; the development and execution of scientific and educational programs aligned with the Brand Medical Plan; delivery of medical and scientific insight back to the CVRM Brand Teams; and identification and targeting of key clinical investigators for key clinical trials.
Essential Skills/Experience:
Advanced degree (M.D., PhD, PharmD, MBBS) in a science-related field, such as Pharmacology, Pharmacy, Medicine, or equivalent
Over 5 years leading programs in a team environment
Validated understanding of medical strategy, clinical development, and medical science liaison areas
Ability to lead a diverse group of responsibilities
Ability to work efficiently in a cross-functional team environment
Authority technical depth in the disease area
Strategic influencing skills
Highly developed written and verbal communication skills
Well-developed initiative ability
Excellent project management skills
Strong organization and time management skills
Strong analytical and problem-solving skills
Preferred Skills/Experience:
Cardiovascular/Metabolic disease experience
Minimum 5 years experience in a strategy-setting role within Medical Affairs
Global experience within the pharmaceutical industry
Solid understanding of FDA requirements
Excellent digital literacy (Excel, Word, PowerPoint, etc.)
Knowledge of information/technology system
#J-18808-Ljbffr