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Medical Advisor Oncology/Specialty (Saudi National)

Unknown
Riyadh Region, KSA
Mid-Senior
Onsite
Discovered Yesterday
Medical AffairsOncology and specialty therapeuticsSolid tumors, companion diagnostics, or specialty therapeutic areasClinical researchReal-World Evidence and non-interventional studiesInvestigator-initiated studies
Free

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Medical AffairsOncology and specialty therapeuticsSolid tumors, companion diagnostics, or specialty therapeutic areas
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Company Description

AbbVie develops medicines and solutions for serious health issues across areas including immunology, oncology, neuroscience, and aesthetics.

Primary Function

Represent the affiliate as a medical and scientific expert for assigned products and therapeutic areas.

Provide expert advice to healthcare customers and develop professional relationships with external experts.

Support medical affairs strategy, commercial planning, cross-functional teams, and affiliate medical activities while maintaining functional independence.

Medical Affairs Responsibilities

  • Support brand team strategy and execution with medical and scientific input.
  • Maintain in-depth product and therapeutic-area knowledge through internal training, congresses, seminars, and literature review.
  • Provide scientific advice and contribute to accurate dossiers, medical information packs, clinical expert reviews, and evidence materials.
  • Develop relationships with external experts and academic centers through congresses, advisory boards, round tables, and discussion forums.
  • Deliver scientific presentations and medical education to healthcare professionals.
  • Train sales forces and other departments and maintain relevant training materials.
  • Screen scientific literature and conference information and summarize important developments.
  • Review promotional and non-promotional materials for scientific accuracy, balance, fairness, and compliance.

Clinical Research Activities

  • Design and implement clinical research projects within defined standards and budgets, including Phase IV, registries, epidemiological surveys, and post-marketing studies.
  • Oversee the review, approval, and conduct of investigator-initiated studies.
  • Support clinical study management, including protocol review, investigator and site identification, and feasibility surveys.

Strategy and Compliance

  • Provide input into product- or therapeutic-area-specific medical affairs plans and local commercial plans.
  • Act as a scientific interface for healthcare professionals, institutions, external experts, professional associations, payers, and regulators.
  • Provide strategic and operational support for clinical research, healthcare professional interactions, scientific data communication, education, and patient safety.
  • Follow applicable laws, regulations, codes of conduct, company policies, procedures, and standards of best practice.

Location and Work Pattern

  • The role is based in Riyadh and is hybrid in nature.
  • Up to 50% of an individual's time may be spent working in the field.

Qualifications

  • A relevant undergraduate degree is required; an advanced degree such as PharmD, PharmB, MD, or PhD is preferred.
  • At least two years of Medical Affairs experience is required.
  • Experience in solid tumors, companion diagnostics, or specialty therapeutic areas is required.
  • Experience in evidence generation, including Real-World Evidence, non-interventional studies, registries, or investigator-initiated studies, is required.
  • Expertise in clinical research methods and applicable legislative and regulatory controls is required.
  • Excellent written and spoken English, communication, presentation, collaboration, planning, and organizational skills are required.
  • Regular travel of approximately 50% is required.
  • Experience in cross-functional or matrix organizations is advantageous.

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