Medical Affairs Senior Advisor

Medical Affairs Senior Advisor/Manager - 06 months contract - £43.68 p/h to £58.24 p/h (Depending upon experience) Job Description: Medical Affairs (Senior) Advisor/Manager If you are innovative and passionate about healthcare and want a role where you can drive change and make a difference, this could be one for you.
In the Specialty Care Business Unit, we have a broad portfolio and pipeline of medicines, including those for Rare Diseases, Inflammation & Immunology and Antibiotics for difficult to treat, resistant infections.
This role is an excellent opportunity to work in a high-performing friendly team, and providing assistance on projects involving product launches within the Rare Haematology Team.
Role Main Responsibilities and Duties To provide medical and scientific advice to healthcare professionals and professional bodies through scientific communications and assistance for clinical research to facilitate a medical and scientific bridge between Company and the healthcare community.
To provide specialist medical, scientific and Code compliance advice to the nominated internal team(s) to promote the appropriate use of Company medicines and successful implementation of Company's initiatives and programs.
Certain roles may emphasise different elements of the role description based on medical and business need.
Partnerships: Activities to build and develop enduring external relationships facilitating a medical and scientific bridge between Company and the healthcare community.
• To provide specialist medical and scientific advice to the nominated internal teams to assist the appropriate use of Company medicines and successful implementation of Company's initiatives and programs.
• To provide medical and scientific advice to healthcare professionals and professional bodies through scientific communications and assistance for clinical research to facilitate a medical and scientific bridge between Company and the healthcare community and academia.
• To liaise with healthcare professionals to effectively convey and manage drug safety issues.
• To build and develop enduring peer-to-peer relationships with influential healthcare professionals and specialists, including non-traditional customers and key decisionmakers.
• To comprehend customer insights around current standard of care and to assist their knowledge of the value of our medicines to the NHS and patients.
Data generation and publication and assistance for clinical development: Shape development program through insights from academic and clinical community and patients.
Generate and publish real world data.
Data generation and publication: • To acquire and maintain in-depth scientific knowledge of Company medicines within nominated therapy area(s) (including those in development) as well as of key competitors.
• To deliver the medical plan in relation to medical projects, Investigator Sponsored Research (ISR) and assistance for Company sponsored clinical research.
• To deliver other key medical and scientific activities within the medical plan, e.g.
generation of real world evidence, non-interventional studies, database studies and registries (in partnership with Access & Value colleagues) and ensure timely publication of data.
Support for clinical development: • To provide medical/scientific input into protocol feasibility assessments for clinical trial proposals.
• To identify appropriate investigators / sites for Company-sponsored clinical trials.
• To work collectively with clinical research colleagues and in conjunction with above-country and global BU colleagues to drive the timely completion of Company-sponsored clinical trials.
• To provide input into the global clinical teams to ensure design and selection of trials relevant to UK needs, leveraging customer and patient insights.
• To assist the effective implementation of approved compassionate use and named patient supply programs to ensure appropriate access to Company medicines in response to HCP requests.
Data communication and customer insights: Convey the value of our medicines through high-quality, accurate, balanced and impactful information.
Utilise customer intelligence and insights to shape brand strategy.
• To provide high-quality, accurate, balanced and specific information to customers in reply to unsolicited requests for information.
• To provide scientific insight and assistance to field- and head office based commercial colleagues.
• To work with the cross-functional team in-country and above-country to develop impactful and compliant promotional and non-promotional materials of value to customers.
• To review (and certify where applicable) promotional and non-promotional materials and activities within scope of the ABPI Code of Practice.
• To ensure customer intelligence is brought into the organisation to generate customer insights, shape future strategy and influence business opportunities.
• To manage local advisory boards to gain customer insights.
• If media-trained, to present the scientific perspective on selected topics during media-briefings.
Cross functional medical and scientific advice: Assistance for other departments including Regulatory Affairs, Drug Safety, Medical Information, Access & Value, Corporate Affairs, Customer Operations, Medical Quality Oversight, Worldwide Research and Development and Clinical Operations.
• Assist Access & Value in providing medical input for HTA dossiers and regional/local formularies.
• Advise Regulatory Affairs in replying to questions from regulatory agencies and implementing changes to product SPC, PIL and PI.
Provide assistance for clinical overviews, core datasheet revisions, licence variations, batch specific variations and implementation of Risk Management Plans.
• Provide assistance to Medical Information to facilitate the maintenance of an accurate, relevant and high-quality database which would enable them to reply effectively to customer enquiries.
• Provide scientific input to other departments (e.g.
Policy & Public Affairs, Stakeholder Strategy, Communications, Customer Operations, Medical Quality Oversight, Research and Development groups) on a project-by-project basis.
• To provide specialist ABPI Code compliance advice to brand/therapy area teams and other departments on customer engagement and partnership activities (e.g.
Digital Programs, Joint Working, Medical & Educational Goods & Services, Advisory Boards).
• To develop and maintain ongoing cross-functional working relationships with colleagues within the in-country and global BU organisations.
REQUIRED SKILL SET • Fluency in Business English • Medical, Pharmacy or Science degree • For medical applicants GMC registration with a Licence to Practice is preferred.
Doctors registered outside the UK may be considered, for example if they have significant pharmaceutical industry exposure and/or have worked in the UK National Health Service.
A postgraduate degree (e.g.
PhD) or evidence of relevant practice or productivity is preferred.
• For pharmacy applicants UK registration is preferred.
Pharmacists registered outside the UK may be considered, for example if they have significant pharmaceutical industry practice and/or have worked in the UK National Health Service.
A postgraduate degree (e.g.
PhD) or evidence of relevant practice or productivity is preferred.
• For scientists a post graduate science degree (eg PhD, MSc) is preferred.
Scientists without this may be considered, for example if they have significant pharmaceutical industry experience in Medical Affairs and/or significant practice within a related specialty (e.g.
clinical research, medicines regulation, health technology assessment).