Medical Advisor Hematology MSD

Key Responsibilities:

• Medical Strategy and Planning:

Develop and execute the KSA hematology medical plan aligned to brand strategy and local market needs. Identify scientific gaps and medical education needs, feed insights into brand planning and lifecycle management.

Execution of 70% field-based interactions.

• External Expert Engagement:

Build and maintain peer-to-peer relationships with KOLs, academic centers, and professional societies across hematology.

Conduct fair, balanced scientific exchange, capture insights, and translate them into actionable plans.

Support advisory boards, speaker programs, and scientific roundtables in full compliance.

• Evidence Generation and Data Dissemination:

Lead/support local research (IIS/ISR, RWE, registries, non-interventional studies) and collaborate on regional/global trials.

Partner with Clinical Operations on feasibility, site identification, and medical oversight in KSA.

Interpret and present clinical data; contribute to publication plans and scientific communications.

Collaborate on HEOR/RWE projects relevant to access, guidelines, and reimbursement.

• Medical Information and Scientific Support:

Provide timely, accurate, balanced medical information; handle unsolicited requests compliantly.

Train CFT teams on disease area, product science, and competitive landscape.

Review and approve promotional and non-promotional materials per SFDA and internal SOPs.

• Patient Access and Cross-Functional Collaboration:

Partner with Market Access on value propositions, evidence needs, and payer engagements.

Collaborate with Regulatory on SFDA submissions, labeling, and commitments.

Support Pharmacovigilance with medical review of ICSRs and aggregate safety data as needed.

• Medical Education and Congresses:

Lead CME programs, workshops, tumor boards; coordinate medical presence at national/regional congresses. Ensure scientific booths, symposia, and materials meet ethical and compliance standards.

• Compliance and Governance:

Adhere to SFDA regulations, Saudi anti-commercial bribery law, industry codes (e.g., IFPMA/PhRMA), and company policies. Maintain high standards of ethics, transparency, and documentation.