•Adapt and Execute of a strategic ERC plan consistent with the Global Corporate Guideline's and aligned with local needs and requirements•Provide active guidance to the business partners on ERC matters, including interactions and practices with health care professionals, government/public officials, health care institutions, patients and patient associations• Support in assessing and monitoring ERC policy/risk areas based on applicable regulations, codes, and country/region risk profile; creates thorough analytic re-views and management reports.• Execute monitoring plans in collaboration with R&A team based on the risk assessment and ensure that results are communicated to the local leadership team and Corporate ERC• Ensure allegations of misconduct are timely reported pursuant to established protocols• Leading the local governance committees• Actively follow compliance trends in the market and regulatory environment including business practices and evolving compliance related legislation• Support as required investigations of alleged misconduct based on allocation of responsibility by the Global SpeakUp Team

Receiving, screening and validation of the medical enquires which submitted to Medical Information department and create the record on Novartis medical enquires management system in addition to assign the valid enquires to the relevant TAHs

Organize and Execute Scientific Activities:• Planned and executed of medical affairs strategic and tactical plans for Neuroscience therapy area• Led and organized MS brand prelaunch and launch.• Developed and Executed Medical activities (Master class, Ad.Boards and International and National Speaker led tours)• Review promotional materials and ensures materials alignment with Novartis Medical code of conduct guidelines from scientific and ethical point of view.• Leading Medical affairs in cross-functional & cross-therapeutic area projects with other functions (Market Access, Marketing and KAMs).• Identified and executed opportunities for productivity and/or efficiency improvement with appropriate colleagues/MSLs/ Cross-functional team.• Ensure providing suburb medical inputs in integrated product planning and strategy.• Attended regular local/ regional/ global meetings/teleconferences to review ongoing local studies progress (recruitment, sites performance... etc.) and instigate appropriate measures.• Designed, planning and implementing local events with full alignment with updated SOPs and regulations.Local Medical Experts Development:• Worldwide ME engagement in local scientific platforms to support local medical strategy execution.• Maintain top ME management. Keep strong relationship with scientific associations. Coordinate the collection and reporting of consolidated ME insights that may affect Novartis development plans, trial designs, launch strategies and tactics and any Cl data.• Align with MSLs colleagues on the medical expert development plan and follow up on execution.Clinical Research Support:• Defined and managed local phase IV clinical activities in collaboration with the clinical research team. Advise the clinical research team on study sites and investigators.• Prepare study documents for local studies and get it approved.

Compiled data for analysis and developed tracking and reporting.Managed own work assignments under general supervision to complete self-assessments and other assigned reviews and projects.In charge of working on improving operations and processes through ensuring application of SOPs.Responsible with coordinating and scheduling required compliance training for employees.Performed regular self-audits over medical affairs to ensure good according to compliance and ethical standards.

Organize and Execute Scientific Activities:• Planned and executed of medical affairs strategic and tactical plans for Ophthalmology specialty.• Led and organized Dry eye portfolio brand prelaunch and launch.• Developed and Executed Medical activities (Master class, Ad.Boards and International and National Speaker led tours)• Review promotional materials and ensures materials alignment with Novartis Medical code of conduct guidelines from scientific and ethical point of view.• Leading Medical affairs in cross-functional & cross-therapeutic area projects with other functions (Market Access, Marketing and KAMs).• Identified and executed opportunities for productivity and/or efficiency improvement with appropriate colleagues/MSLs/ Cross-functional team.• Ensure providing suburb medical inputs in integrated product planning and strategy.• Attended regular local/ regional/ global meetings/teleconferences to review ongoing local studies progress (recruitment, sites performance... etc.) and instigate appropriate measures.• Designed, planning and implementing local events with full alignment with updated SOPs and regulations.Local Medical Experts Development:• Worldwide ME engagement in local scientific platforms to support local medical strategy execution.• Maintain top ME management. Keep strong relationship with scientific associations. Coordinate the collection and reporting of consolidated ME insights that may affect Novartis development plans, trial designs, launch strategies and tactics and any Cl data.• Align with MSLs colleagues on the medical expert development plan and follow up on execution.Clinical Research Support:• Defined and managed local phase IV clinical activities in collaboration with the clinical research team. Advise the clinical research team on study sites and investigators.• Prepare study documents for local studies and get it approved.

• To serve as a liaison to medical/scientific community and responsible for establishing, developing and collaborating with Health Care Professionals (HCPs).• To implement clinical and educational strategies in collaboration with other Novartis colleagues for designated stakeholders.

Conducting an induction training for new hires and refreshment training for Retina Field Force.

Worked as product specialist responsible for Retina Product (Lucentis)

Worked as product specialist responsible for Ophthalmology Product (Lucentis)

Medical Rep responsible for promoting NSAIDS