Medical Science Liaison

In this field-based position you will represent AbbVie Medical Affairs as subject matter expert in oncology covering the Western region of Czech Republic.  In your role you will: 

• Provide scientific and technical leadership to ensure professional and credible relationships with external experts /HCPs of strategic importance to Abbvie. 
• Serve as a point of contact within the Medical Affairs team for external experts within the assigned geographic area to satisfy their needs for scientific knowledge in a therapeutic area and, when requested, relevant AbbVie medicines, to support their safe, effective and appropriate use. 
• Develop and execute scientific interaction plans, cycle plans; contribute to cross-functional account planning, as appropriate. 
• Responsible for appropriate tiering and segmentation of external experts based on guidance from the IFT playbooks and appropriate documentation of HCP interactions and relevant insights in the CRS and related platforms and systems.   
• Ensure a strong medical and scientific presence for Abbvie in key academic centers by facilitation of research and educational initiatives, while supporting requests for medical and scientific information on products or areas of therapeutic interest to Abbvie. 
• Work closely together with your Medical Advisor colleagues and support internal teams such as sales and marketing and members of the Affiliate Brand Team to develop their scientific and technical expertise through the delivery of scientific update presentations.  Work collaboratively and cross-functionally with other in-field members while retaining functional independence. 
• Assist in the initiation, oversight and follow up of assigned GMA studies and medical projects initiated within the therapeutic area for which the MSL carries responsibility (e.g. registry/database projects, epidemiological studies, post-authorization studies (PMOS) 
• Support prioritized interventional studies run by Clinical Development Operations, with study initiation visits and act as subject matter expert as part of One R&D community.  All such activities must comply with applicable local laws, guidelines, codes of practice, SOPs, and AbbVie R&D SOPs. 
• Act as the point of contact with external experts to facilitate investigator-initiated study (IIS) ideas and requests for support to the local and global medical teams as appropriate. 
• Deliver credible presentations on scientific matters to physicians, individually or in groups (meetings, clinical sessions, etc.), where requested, but with the focus on thought leaders. 
•  Attend relevant scientific meetings and Conferences.  Collaborate with internal stakeholders to develop summaries of key data and other scientifically relevant information to inform AbbVie strategic priorities and initiatives.  
• Upon request, assist physicians with requests for access to AbbVie medicines on a named patient or compassionate use basis, subject to all applicable legal and regulatory requirements. 
• Provide key thought leaders / external experts and internal medical and clinical teams with scientific and technical support for publications of scientific or medical interest. 
• Ensure that all activities and interactions are conducted with due regard to all applicable local, global, and national laws, regulations, guidelines, codes of conduct, Company policies and accepted standards of best practice.