Medical Science Liaison - Northern Region
Hemel Hempstead, GB
Job Purpose
Reporting to the Medical Director, the Medical Scientific Liaison (MSL), will lead the medical and scientific activities within the Northern region of the UK to inform and educate physicians, support staff, payers and any other relevant industry groups on Recordati’s portfolio. The MSL must also support and comply with all relevant internal and external regulations, guidelines and policies at both local and international level
Key Responsibilities
Scientific Expertise
- To established as an internal and external product and disease area expert including treatment guidelines, protocols, engage in discussions on and support clinical research projects including real world data studies.
- To respond in a timely manner to unsolicited requests from healthcare professionals for medical/scientific information.
- To communicate and disseminate scientific information across the internal and external stakeholder groups.
- To deliver internal and external product and disease state training as required.
- To monitor and maintain up to date knowledge on all products and company’s activities relevant to the disease area.
- Responsibility for attending national and international scientific meetings, as required, to gather current scientific information and to address HCP’s unsolicited questions.
KOL Management
- To serve as the primary scientific contact with Health Care Professionals at a Regional or National level on the specific disease area(s).
- To support clinical development activities in the assigned therapy area(s).
- To organise and engage in medical interactions with KOLs.
- To build relationships with external experts (e.g. Health Care Professionals, Payers, Patient groups), through robust, scientific dialogue
- To work cross functionally to connect KOLs with other internal and external parties as appropriate.
- To support specific events as required by the company including KOL led meetings and medical symposia, advisory board meetings and congresses.
- To identify and develop potential areas of medical collaboration with KOLs.
- To work with the local, regional, national and international collaborative groups, guidelines committees as needed to ensure accurate and timely dissemination of product and disease state information.
- To identify suitable publication projects through ongoing relationships with KOLs.
- To engage in discussions on and support clinical research projects including real world data studies.
Territory Management
- To maintain knowledge on current treatment pathways, protocols and practices across defined geographical area.
- To ensure and up to date knowledge of hospitals, KOLs, competitor activities, studies, trends, influencers, formularies, buyers, reimbursement providers across area.
- To support clinical development activities in the assigned therapy area if relevant (such as site identification and assessment; safety and product training for external clinical trial teams; addressing study subject retention and other scientific issues in partnership with the clinical operations and medical teams).
Organisational Effectiveness
- To take ownership of medically led projects as agreed with the Senior Medical Affairs Director.
- To represent the medical department at national and international meetings, congresses and symposia, draft and collate reports from relevant sessions.
- To work within the policies and procedures of Recordati’s internal and external regulations at all times.
- To act as an ambassador for Recordati at all times.
- To produce and implement a comprehensive annual Medical and Scientific plan that anticipate and support the requirements for product and disease information. Where and when necessary, make swift changes to address changing customer needs.
- To track and manage OPEX in line with the approved budget.
Required Education
Accredited Health Care Professional (Pharmacist) or Life Science Degree., PhD or MSc
Required Skills and Experience
Ability to tailor communication across multiple Health Care Professional groups
In depth knowledge of market access and clinical approval processes within the geography
Technical Competencies
Experience in interpretation and writing of scientific information.
Required Behaviours and Competencies
Strong communicator in a one to one and group setting, verbal and non-verbal using appropriate industry and medical language.
Monitor and ensure compliance with company policies.
Excellent project planning, organisation, implementation and tracking skills.
Required Languages
Fluent in English both written and spoken.
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Travel required in %
70%