Scientific Liaison Specialist

5 days ago

Riyadh, Ar Riyāḑ, Saudi Arabia Qataryello Full time

At Qataryello, we are seeking a highly skilled Scientific Liaison Specialist to join our medical affairs team in Riyadh. This role will play a pivotal part in advancing our aesthetics portfolio, focusing on scientific education, pharmacovigilance, and key opinion leader engagement within Saudi Arabia.

The ideal candidate for this position will bridge the gap between internal and external stakeholders, ensuring seamless dissemination of clinical data and supporting our organization's strategic initiatives in the region.

Key Responsibilities:
  1. KOL & Trainer Engagement: Establish and maintain relationships with key opinion leaders (KOLs) and trainers, providing 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 our company strategy.
  3. Scientific & Medical Education: Provide training to internal teams on the scientific and clinical aspects of our 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.
  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 should possess a scientific or medical background, be a Saudi National (preferred), hold a degree in Pharmacy (Bachelor or Master), have over 3 years of experience in the pharmaceutical or medical device industry as an MSL, exhibit excellent English communication skills, and demonstrate strong business acumen to analyze and interpret clinical studies.

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