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SalaryDate: 14 Mar 2024
Department: Medical Affairs
Team: Mktg, Market Access, Bus. Excellence & Med. Affair
Job Type: Direct Employee
Contract Type: Permanent
Location:
Manchester, GB
Purpose
The role provides non-promotional medical and scientific support for the Chiesi UK business, with the aim of providing high quality, accurate and timely scientific advice to healthcare professionals regarding the company’s products and associated disease area(s).
MSLs contribute to the development and implementation of Chiesi strategic planning for the UK by providing medical insight and applying expert knowledge about the product and/or disease area and by identifying, developing and maintaining credible relationships with Key Opinion Leaders (KOLs) and academic centres.
The role functions a non-promotional capacity for 100% of the time and is field-based.
The role is based primarily in the North
This role is on a secondment basis for 12 months
Candidate 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, whilst possessing the ability to work both independently or 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.
Main Responsibilities
Provide fair, balanced and unbiased field-based medical and scientific support 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 relevant disease area(s) to be the expert medical resource
Contribute to the development and implementation of the UK Medical Affairs strategic plan, including but not limited to: 1. Design and execute Medical Educational meetings 2. Gather Insights from relevant KOLs and feed competitive insights back to 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 enquiries from healthcare professionals
Produce and update scientific and clinical presentations for assigned therapeutic area(s) as appropriate
Work with Learning and Development to provide support for the provision of training the commercial teams at national and international sales meetings
Develop proficiency in the technical review of materials and/or activities on 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
Qualifications and Experience Required
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
Key Requirements and Skills
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
Organised with systematic approach to prioritisation
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 role to support the UKI Medical Affairs plan and to attend domestic and international conferences. Occasional weekend travel will be required
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