Senior Medical Advisor - Immunology (Rheumatology)
Apply locations: UK, Basingstoke Time type: Full time Posted on: Posted Yesterday Time left to apply: End Date: February 9, 2025 (9 days left to apply) Job requisition id: R-79199 At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world. Senior Medical Advisor - Immunology (primarily Rheumatology) UK and Ireland Primarily responsible for Rheumatology, but also involved in Dermatology and Gastroenterology Reporting to: Immunology Lead UK & Ireland Location: Hybrid (Basingstoke, UK) 3 days per week Due to a recent promotion within our organisation, we now have an exciting opportunity for you to join Eli Lilly as a
Medical Advisor / Clinical Research Physician / Scientist (CRP/S) for Immunology UK and Ireland. Qualifications and experience: An advanced medical/scientific or related graduate degree such as MD, PharmD, PhD (qualifications related to Immunology preferred). 1+ years experience in Medical Affairs Immunology essential. Medical Advisor experience in immunology preferred, particularly within rheumatology. Final signatory capabilities preferred. Other Skills: Strong understanding of medical’s role in the cross-functional team, and willingness to contribute to the cross-functional work needed to best support our immunology brands. Demonstrated ability to balance scientific priorities with business priorities. Strong communication, interpersonal, teamwork, organizational and negotiation skills. Successful track record of developing and delivering high-quality medical activities via an omni-channel approach. Ability to engage in domestic and international travel to the degree appropriate to support the business and the team. Knowledge and expertise of the UK ABPI code. Fluent in English, verbal and written communication. Responsibilities: Business / customer support (pre and post launch support) Understand and anticipate the scientific information needs of all local/regional customers (payers, patients, health care providers). Actively address customer questions in a timely fashion by leading data analyses and new clinical or health outcomes research efforts. Contribute to the development of medical strategies to support brand commercialisation activities. Contribute as a scientific and medical expert to activities and deliverables of the PRA organisation, particularly giving clinical input and insight to develop payer partnership programs and defend the product value. Contribute actively on an ongoing basis to the strategic planning for currently marketed brands. Offer scientific and creative input, contribute to the development, review, and approval of promotional materials for the brand team. Support training of sales representatives, and other medical representatives. Scientific Data Dissemination / Exchange Knowledge of compliance with local laws and regulations, and global policies and procedures, compliance guidelines with respect to data dissemination and interactions with external health care professionals. Review and approve promotional and non-promotional materials in line with local compliance guidelines. Support the planning of symposia, advisory board and medical meetings. Support medical information associates in preparation and review of medical letters and other medical information materials. Support the development of educational programmes and digital omni-channel capabilities. Support training of local medical personnel. Prepare or review scientific information in response to customer questions or media requests. Support data analysis and the development of slide sets. Develop and maintain appropriate collaborations and relationships with relevant professional societies. Clinical Planning Communicate and collaborate to ensure life cycle plans for drugs in development address customer needs. Collaborate with other regions and the global teams. Regulatory Support Activities Participate in development and review of local labelling and labelling modifications. Provide medical expertise to regulatory scientists. Support / assist in the preparation of regulatory reports. Scientific / Technical Expertise and continued development Be aware of current trends and projections for clinical practice. Keep updated with medical and other scientific developments relevant to the product. Embracing diversity is at the core of our long-held value of respect for people. It is the lens through which we understand and respond to the unique needs of the millions of individuals who depend on our medicines. For us, embracing diversity means understanding, respecting, and valuing differences, including but not limited to race, colour, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other legally protected status. Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status. #WeAreLilly
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Apply locations: UK, Basingstoke Time type: Full time Posted on: Posted Yesterday Time left to apply: End Date: February 9, 2025 (9 days left to apply) Job requisition id: R-79199 At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world. Senior Medical Advisor - Immunology (primarily Rheumatology) UK and Ireland Primarily responsible for Rheumatology, but also involved in Dermatology and Gastroenterology Reporting to: Immunology Lead UK & Ireland Location: Hybrid (Basingstoke, UK) 3 days per week Due to a recent promotion within our organisation, we now have an exciting opportunity for you to join Eli Lilly as a
Medical Advisor / Clinical Research Physician / Scientist (CRP/S) for Immunology UK and Ireland. Qualifications and experience: An advanced medical/scientific or related graduate degree such as MD, PharmD, PhD (qualifications related to Immunology preferred). 1+ years experience in Medical Affairs Immunology essential. Medical Advisor experience in immunology preferred, particularly within rheumatology. Final signatory capabilities preferred. Other Skills: Strong understanding of medical’s role in the cross-functional team, and willingness to contribute to the cross-functional work needed to best support our immunology brands. Demonstrated ability to balance scientific priorities with business priorities. Strong communication, interpersonal, teamwork, organizational and negotiation skills. Successful track record of developing and delivering high-quality medical activities via an omni-channel approach. Ability to engage in domestic and international travel to the degree appropriate to support the business and the team. Knowledge and expertise of the UK ABPI code. Fluent in English, verbal and written communication. Responsibilities: Business / customer support (pre and post launch support) Understand and anticipate the scientific information needs of all local/regional customers (payers, patients, health care providers). Actively address customer questions in a timely fashion by leading data analyses and new clinical or health outcomes research efforts. Contribute to the development of medical strategies to support brand commercialisation activities. Contribute as a scientific and medical expert to activities and deliverables of the PRA organisation, particularly giving clinical input and insight to develop payer partnership programs and defend the product value. Contribute actively on an ongoing basis to the strategic planning for currently marketed brands. Offer scientific and creative input, contribute to the development, review, and approval of promotional materials for the brand team. Support training of sales representatives, and other medical representatives. Scientific Data Dissemination / Exchange Knowledge of compliance with local laws and regulations, and global policies and procedures, compliance guidelines with respect to data dissemination and interactions with external health care professionals. Review and approve promotional and non-promotional materials in line with local compliance guidelines. Support the planning of symposia, advisory board and medical meetings. Support medical information associates in preparation and review of medical letters and other medical information materials. Support the development of educational programmes and digital omni-channel capabilities. Support training of local medical personnel. Prepare or review scientific information in response to customer questions or media requests. Support data analysis and the development of slide sets. Develop and maintain appropriate collaborations and relationships with relevant professional societies. Clinical Planning Communicate and collaborate to ensure life cycle plans for drugs in development address customer needs. Collaborate with other regions and the global teams. Regulatory Support Activities Participate in development and review of local labelling and labelling modifications. Provide medical expertise to regulatory scientists. Support / assist in the preparation of regulatory reports. Scientific / Technical Expertise and continued development Be aware of current trends and projections for clinical practice. Keep updated with medical and other scientific developments relevant to the product. Embracing diversity is at the core of our long-held value of respect for people. It is the lens through which we understand and respond to the unique needs of the millions of individuals who depend on our medicines. For us, embracing diversity means understanding, respecting, and valuing differences, including but not limited to race, colour, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other legally protected status. Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status. #WeAreLilly
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