Medical Science Liaison

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We have an exciting opportunity for a Medical Science Liaison (MSL) to join our Medical Affairs team.

At Chiesi, it is our people who are at the heart of what we do and achieve. A proud family business, we are a Top Employer and a Great Place to Work in the UK.

In the role of MSL, you will proactively engage healthcare professionals and other external stakeholders at all levels of the NHS by providing information that is of high quality, accurate, and timely. The MSL not only reacts to medical information requests for balanced information but also initiates high-level medical, scientific, and clinical discussions, using a non-promotional approach.

MSLs contribute to the development and implementation of Chiesi's strategic planning for the UK by providing medical insight and applying expert knowledge about the product and/or disease area, identifying, developing, and maintaining credible relationships with Key Opinion Leaders (KOLs) and academic centres.

The role functions in a non-promotional capacity for 100% of the time and is field-based.

Profile

This role requires a blend of strong scientific/clinical expertise and a high level of communication skill. It is essential that MSLs are self-starters with a high level of motivation, possessing the ability to work both independently and as part of a team as the situation demands. Thorough knowledge of the allocated therapeutic and disease area(s) is essential, as is a comprehensive knowledge of the ABPI Code of Practice to ensure that all activities undertaken are conducted in a non-promotional manner. A working knowledge of the pharmaceutical industry and a thorough understanding of the wider NHS environment is highly desirable.

Responsibilities

• Provide fair, balanced, and unbiased field-based medical and scientific support both proactively and in response to specific requests from healthcare professionals for further information around Chiesi’s product portfolio, clinical development program, or disease area(s) of interest.
• Identify, develop, and maintain professional and credible relationships with the health care community, especially Key Opinion Leaders (KOLs) and academic centres, in the relevant disease area(s) and in collaboration with relevant internal functions.
• Develop and maintain in-depth knowledge of relevant products and disease area(s) to be the expert medical resource.
• Contribute cross-functionally to the development and implementation of the UK AIR/RARE/CARE business plans, including but not limited to:
• Design and execute the Medical Educational programme(s).
• Gather insights from relevant KOLs and feed competitive insights back to the wider medical team.
• Project management of UK investigator-initiated trial (IIT) applications, ensuring that all IIT applications are carried out in compliance with applicable UK regulations and Chiesi SOPs.
• Provide local input into company-sponsored UK Phase II-IV clinical development activities, as required.
• Attend relevant national and international scientific meetings/congresses to ensure up-to-date knowledge of therapy area, gather competitive intelligence, and respond to any specific inquiries from healthcare professionals.
• Produce and update scientific and clinical presentations for assigned therapeutic area(s) as appropriate.
• Provide expert support and internal training of key clinical evidence to the XF team.
• Develop proficiency in the technical review of materials and/or activities on the internal approval system.
• Ensure compliance with all statutory requirements, internal processes, and procedures for Pharmacovigilance.
• Ensure that all activities and interactions are conducted in compliance with applicable local, global, and national laws, regulations, guidelines, codes of conduct (including but not limited to the ABPI Code of Practice), company policies, and accepted standards of best practice.

• A medical/pharmacy degree or PhD preferably or BSc qualification.
• Demonstrable relevant Industry experience, including proven ability to engage with KOLs.
• In-depth knowledge of ABPI Code of Practice, preferably with final signatory status.
• Good working knowledge of the clinical trial process, including the regulations pertaining to phase III/IV clinical study management and conduct.
• Good understanding of Good Clinical Practice (GCP) and Good Pharmacovigilance Practice.
• Understanding of the wider NHS environment and key opportunities for pharma and the NHS to partner effectively within the scope of the ABPI Code of Practice.

• Resilience with the ability to deliver in a challenging external environment.
• Ability to engage and manage multiple stakeholders (both internal and external) to achieve the objective(s).
• Curious with learning agility.
• Organized with a systematic approach to prioritization.
• Strong communication and presentation skills.
• Excellent interpersonal skills with confidence to engage stakeholders at all levels.
• Ability to work effectively both independently as well as part of a team, as the situation demands.
• Ability to interpret and present complex clinical data in a clear manner to a variety of audiences.
• Drive to continuously expand medical and scientific knowledge.
• Ability to travel as part of the role to support the UKI Medical Affairs plan and to attend domestic and international conferences. Occasional weekend travel will be required.

Seniority level

• Entry level

Employment type

• Full-time

Job function

• Research, Analyst, and Information Technology
• Industries: Pharmaceutical Manufacturing