Job Brief:

Provides answers to medically and scientifically based questions and maintains longstanding scientifically based relationships with medical community: KOLs and Mid-Senior Clinicians, different Medical and Academic Institutions, Regulatory Authorities. Review promotional materials and keep adherence to relevant regulatory requirements and company Standard Operating Procedures (SOPs) as appropriate for all scientific activities. Responsible for providing updated medical and scientific data about TA and relevant Products to different internal stakeholders within the organization.

Major Accountabilities:

• Medical expert with (80%) field-based role within medical affairs department
• An integral position in communicating accurate, clear, and valued information regarding our clinical trials data, products, and relevant Therapeutic Areas to multiple levels within the medical community and is responsible for providing field observations to internal stakeholders.

Responsibilities & Duties:

• Support and provide scientific nonbiased information and data relevant to Therapeutic Area, and Pharmaceutical Products to external stakeholders (KOLs, Academic Institutions, Regulatory Authorities, etc..) to ensure safe effective utilization of Products, to advance the scientific platform as aligned with the corporate goals and objectives.
• Maintain scientific collaboration with KOLs, Clinicians, Academic Professors, and engaging them in educational activities like CME training programs, symposia, advisory boards, patients\' education and awareness programs, clinical trials updates relevant to TA and company\'s pipeline.
• Support, congress activities as aligned with company\'s strategy.
• Identify speakers, and rising Opinion Leaders to be engaged in speakers\' bureau by training and supporting them with all needed clinical trials and TA data.
• Responding to unsolicited requests for medical information from physicians and healthcare providers relevant to company\'s products, or pipeline products, as per company\'s SOPs and Compliance standards.
• Gathering insights from healthcare and medical community regarding feedback, TA related information to identify patient\'s journey, treatment, and diagnostics\' challenges, market intelligence.
• Educate and communicate clinical value, outcomes, and economic data to payers, providers, key stakeholders, advocacy, and access enablers.
• Update and train internal stakeholders on Therapeutic Area, and Products\' clinical trials data, and collaborate with different teams in scientific activities within compliance standards of the company.

Job Requirements:

• Bachelor\'s degree, Physician or Pharmacist.
• Minimum 3 years field experience in specialty TA with reputable pharmaceutical company including minimum 1-year MSL / Product Specialist.
• TA Ophthalmology or Rare Diseases experience is preferable.
• Geographical experience in UAE is a must.

Antal International