Abraham Dauda Email & Phone Number

• Lead strategic planning and execution of medical affairs activities within Neurology, ensuring alignment with overall business objectives.• Cultivate and maintain relationships with key opinion leaders (KOLs), healthcare professionals (HCPs), and academic centers to support research initiatives and product endorsements.• Oversee the development and dissemination of clinical and scientific data to HCPs, tailoring communications to meet diverse audience needs and regulatory compliance.• Mentor and train new MSL team members, enhancing team performance and ensuring consistency in scientific messaging and stakeholder engagement strategies.• Collaborate with cross-functional teams, including clinical research, regulatory affairs, and marketing, to support product lifecycle management and market access strategies.• Identify and facilitate investigator-initiated trials (IITs) and collaborative research opportunities that align with company interests and enhance product value.• Provide scientific and technical support for clinical development programs, including protocol development, site selection, and data interpretation.

• Engage with key opinion leaders (KOLs) and healthcare professionals (HCPs) to facilitate scientific exchanges and gather insights to inform medical and clinical strategies.• Present scientific and clinical data to HCPs, supporting the safe and effective use of products within the therapeutic area.• Support clinical trial activities, including site identification, investigator engagement, and patient recruitment strategies.• Respond to unsolicited requests for medical information from HCPs, ensuring compliance with regulatory standards.• Conduct ongoing analysis of the competitive landscape and therapeutic area trends to inform strategic planning.

• Participate in medical conferences, symposia, and advisory boards, representing the company's scientific interests.• Collaborate with cross-functional teams to develop and implement medical education programs and materials.• Provide training and support to internal stakeholders on scientific research, product information, and therapeutic area updates.• Facilitate the development and execution of investigator-initiated trials (IITs) that align with company objectives.• Maintain strict adherence to ethical standards and compliance with all regulatory requirements and company policies.

• Performed on-site and remote monitoring activities, ensuring data accuracy through Source Data• Review (SDR), Source Data Verification (SDV), and CRF review.