? Develop professional relationships, build advocacy and gain supports from KOL/decision makers.
? Responsible for successful execution of KOL engagement plan: Engage and develop more than 30 KOLs to be advocate/advisor for UCB per year;
? Collect, analyze and report insights (CRM System) may impact UCB development plans.
? Provide and discuss scientific information and data to KOL/healthcare professionals to ensure quality and accuracy of medical and scientific information on treatment options including UCB products and selected areas of therapeutic interest.
? Provide reactive response to unsolicited customer requests for product information on off-label indications;
? Facilitate use of standard prepared responses prepared by Global Medical Affairs to answer requests for medical and product information.
? Support clinical trial and development programs
? Identify, develop, maintain and expand communication with key investigators to facilitate appropriate research on pipelines and marketed products.
? Provide support to physicians interested in or involved in IITs (Investigator Initiated Trials) or UCB supported phase IV studies or RWE study;
? As appropriate, support in the design and development of clinical studies.
? Provide internal scientific support
? Ensure optimal collaboration across the assigned Medical team with internal customers, partners and other stakeholders.
? Implementation of UCB SOP, GCP and local policies to ensure medical initiatives to comply to related SOP and regulations
? Understanding and acting in line with UCB legal, regulatory and company standards and codes of practice;
? Inform Local Safety Responsible of safety issues according to UCB safety SOPs; and provide scientific support and follow-up on product safety issues
? Provide comprehensive product/disease and therapies presentations and training to internal and external customers, incl. the field force, for the accurate delivery of messages in line with global plans