Medical Science Liaison

4 weeks ago

Riyadh, Ar Riyāḑ, Saudi Arabia Qataryello Full time

Our client is a global aesthetic multinational looking to recruit a Medical Science Liaison for their team in Riyadh. This position plays a key role in medical affairs, focusing on scientific education, pharmacovigilance, and key opinion leader (KOL) engagement within Saudi Arabia.

The Medical Science Liaison (MSL) will bridge the gap between internal and external stakeholders, ensuring the effective dissemination of clinical data and supporting the organization's aesthetics portfolio. The role aligns with the company's strategic initiatives and medical objectives in the region.

  1. KOL & Trainer Engagement: Identify, establish, and maintain relationships with key opinion leaders (KOLs) and trainers. Provide scientific support and continuous education to enhance their expertise.
  2. Investigator-Initiated Trials & Data Generation: Identify and support healthcare professionals (HCPs) in investigator-initiated trials (IITs) aligned with company strategy.
  3. Scientific & Medical Education: Provide training to internal teams on the scientific and clinical aspects of the product portfolio. Educate external stakeholders on new indications, research findings, and product-related inquiries.
  4. Conferences & Events Support: Facilitate speaker engagements and ensure alignment with conference objectives. Develop briefing materials, support content creation, and oversee honoraria processes.
  5. Medical Projects & Partnerships: Identify and drive educational collaborations that contribute to the development of the aesthetics community. Work cross-functionally with internal departments to implement impactful initiatives.
  6. Cross-Functional Collaboration: Establish strong working relationships across departments, fostering a collaborative work environment.
  7. Compliance & Regulatory Adherence: Ensure strict adherence to company policies, SOPs, and regulatory guidelines regarding medical communications. Monitor and report safety data as per regulatory requirements and internal protocols. Maintain awareness of local regulatory obligations related to reporting adverse events.
  8. Pharmacovigilance & Adverse Event Reporting: Accurately document and report adverse drug reactions (ADR) and serious adverse events (SAE) as per regulations. Act as the primary liaison for collecting and forwarding pharmacovigilance data.
  9. Scientific Communication & Data Dissemination: Regularly review and summarize new clinical studies for internal and external stakeholders. Ensure fair, balanced, and evidence-based scientific discussions.

The ideal candidate for this role will:

  • Have a scientific or medical background
  • Be a Saudi National (preferred)
  • Hold a degree in Pharmacy - Bachelor or Masters in Pharmacy
  • Have over 3 years of experience in the pharmaceutical or medical device industry as an MSL
  • Possess strong business acumen to analyze and interpret clinical studies
  • Exhibit excellent English communication skills
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