AstraZeneca GmbH
Director Medical Affairs, CKD
AstraZeneca GmbH, 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 equivalentOver 5 years leading programs in a team environmentValidated understanding of medical strategy, clinical development, and medical science liaison areasAbility to lead a diverse group of responsibilitiesAbility to work efficiently in a cross-functional team environmentAuthority technical depth in the disease areaStrategic influencing skillsHighly developed written and verbal communication skillsWell-developed initiative abilityExcellent project management skillsStrong organization and time management skillsStrong analytical and problem-solving skillsPreferred Skills/Experience:
Cardiovascular/Metabolic disease experienceMinimum 5 years experience in a strategy-setting role within Medical AffairsGlobal experience within the pharmaceutical industrySolid understanding of FDA requirementsExcellent digital literacy (Excel, Word, PowerPoint, etc.)Knowledge of information/technology systemAre you ready to make a meaningful impact on patients' lives and your personal growth? Join us today!
#J-18808-Ljbffr
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 equivalentOver 5 years leading programs in a team environmentValidated understanding of medical strategy, clinical development, and medical science liaison areasAbility to lead a diverse group of responsibilitiesAbility to work efficiently in a cross-functional team environmentAuthority technical depth in the disease areaStrategic influencing skillsHighly developed written and verbal communication skillsWell-developed initiative abilityExcellent project management skillsStrong organization and time management skillsStrong analytical and problem-solving skillsPreferred Skills/Experience:
Cardiovascular/Metabolic disease experienceMinimum 5 years experience in a strategy-setting role within Medical AffairsGlobal experience within the pharmaceutical industrySolid understanding of FDA requirementsExcellent digital literacy (Excel, Word, PowerPoint, etc.)Knowledge of information/technology systemAre you ready to make a meaningful impact on patients' lives and your personal growth? Join us today!
#J-18808-Ljbffr