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AstraZeneca

Global pharmaceutical company developing prescription medicines

Medical Science Liaison

Clinical Research OperationsPosted on Nov 11
Full-timeKarachi, Karachi City, Sindh, PakistanNo salary listedIn-person

About the Job

Requirements

  • External candidates must have at least 2 years of experience in a Medical Affairs role in the pharmaceutical industry.
  • External candidates must have an established track record of basic or clinical research.
  • Candidates must hold a bachelor's degree in medicine, pharmacy, pharmacology, or biomedical sciences, or a master's degree in a scientific discipline.
  • Candidates must be fluent in English.
  • Candidates must have strong oral and written communication and interpersonal skills.
  • Candidates must be able to communicate internally and externally using different channel mixes.
  • Candidates must be able to learn and acquire scientific concepts and knowledge effectively.
  • Candidates must have project management skills and presentation skills.
  • Candidates must have high-level analytical and conceptual thinking abilities.
  • Candidates must be able to work effectively in a matrix, multicultural organization and cross-functional environment.
  • Internal candidates must have at least 2 years of experience at AstraZeneca, a strong performance record, and no compliance-related issues.

Responsibilities

  • Build, enhance, and maintain advocacy among Key External Experts (KEEs), including non-traditional stakeholders, based on scientific or clinical expertise and influence, and engage them in balanced, objective, and accurate scientific discussions.
  • Identify and prioritize accounts based on patient care pathways, and map multidisciplinary teams and their maturity.
  • Provide the company with insight into the local medical community, clinical practice trends, healthcare professional insights, scientific knowledge gaps, patient journeys, and disease management.
  • Foster scientific partnerships with KEEs to advance disease understanding and evidence-based changes in medical practice aligned with Medical Affairs strategy and objectives.
  • Interact with the medical community on clinical trials, non-interventional studies, investigator-sponsored studies, scientific exchange, and other medical projects.
  • Identify potential speakers and train them for local events as appropriate.
  • Recommend participants for advisory boards and round tables, and serve as faculty or facilitator for advisory board meetings.
  • Present scientific data to healthcare professionals in group medical meetings and one-on-one settings.
  • Facilitate continuing medical education events for healthcare professionals.
  • Support evidence generation in the region in alignment with the disease-area and product medical strategy.
  • Collect and share actionable insights that enhance appropriate use of products and disease management with internal stakeholders.
  • Engage in strategic planning meetings and scientific presentations with medication-access stakeholders, institutional decision makers, and other external stakeholders to support clinical decisions and medication accessibility, keeping scientific discussions separate from promotional and other business discussions.
  • Organize and facilitate scientific events at healthcare institutions for multidisciplinary teams in the therapeutic area to support holistic patient care.
  • Develop an understanding of healthcare systems and patient experiences in priority hospitals and institutions to transform care and improve patient outcomes.
  • Maintain expertise in company products, emerging therapies, competitors, patient and treatment trends, clinical trials, and scientific activities in the disease area.
  • Train internal stakeholders periodically on the therapeutic area, products, local medical community, clinical practices and trends, scientific knowledge gaps, and medical treatment options and guidelines.
  • Provide scientific support at company-sponsored educational events.
  • Plan and execute regional medical activities during product launches.
  • Respond to unsolicited requests for information about unapproved products or unapproved uses of approved products with objective, balanced, substantiated, truthful, non-misleading scientific information free of promotional messages.
  • Document accurate scientific responses to unsolicited healthcare-provider questions in accordance with company policies, applicable laws, regulations, and ethical standards.

Desired Qualifications

  • A doctoral degree in a scientific discipline, such as an M.D., Ph.D., or Pharm.D.
  • Experience in the pharmaceutical industry, regulatory environment, clinical or preclinical research, and knowledge of a therapeutic-area disease state and treatment.
  • Experience with basic research, drug discovery, drug development, and KEE interactions.

About the Company

AstraZeneca

Global pharmaceutical company developing prescription medicines

AstraZeneca develops and markets prescription medicines and vaccines worldwide, with a focus on oncology, cardiovascular/metabolic, respiratory, and infectious diseases. Its products work by targeting specific biological pathways or cells, using small-molecule therapies, biologics, and vaccines to treat diseases or prevent infections. It differentiates itself through its dual heritage from Sweden and the UK, a broad pipeline, and strong R&D and collaborations that move from discovery to patient access. Its goal is to improve people’s health by discovering, developing, and delivering medicines and vaccines to patients worldwide.

Company size
10,001+
Company stage
IPO
Headquarters
Cambridge, United Kingdom
Founded
1913

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