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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.

Medical Advisor Oncology

Bringing a deep understanding of the emerging science, key objective of the medical affairs team in Switzerland is to educate physicians and to collect their insights to assemble the scientific evidence, hence, enabling cross-functional teams to focus on programs which are relevant to health care providers (HCPs) and have the biggest impact on patient outcomes.

To strengthen our affiliate medical affairs team, we are looking for a Medical Advisor assuming responsibilities for the clinical advancement of our Oncology/Hematology portfolio.

Purpose of the job:

Through the application of scientific and clinical training and expertise, the Medical Advisor Oncology is an integral member of the medical affairs, development, or a business unit brand team for strategic planning in the support of pre-launch, launch and commercialization activities to meet patients’ needs and ultimately enhance the customers’ experience in interacting with Lilly as a Medicine company.

Core job responsibilities:

In an effort to fully understand external opinions, issues, and new science in the area of oncological diseases medical advisors gather and communicate scientific intelligence, clinical care gaps (CCGs) and scientific gaps (SGs) and other insights identified through their interactions with scientific experts and other health care providers. To foster late-stage product development and to enable patientsÂŽ access to innovative treatments they partner locally across functions (regulatory, marketing, PRA, legal) and with regional/global colleagues to facilitate integrated evidence generation, hence, to better inform Lilly’s strategic direction. Key tasks and responsibilities include:

• Interacting with scientific experts and other HCPs.
• Leading and presenting at conferences, advisory boards, scientific exchange meetings, etc., and overseeing the development of the scientific content of educational programs.
• Participating in the development of the "patient journey" and the strategic plan for the respective compounds.
• Partnering with regional/global teams for integrated evidence generation projects.

Job requirements:

• An advanced health/medical/ scientific (for example, in pharmacology, physiology, microbiology) or related graduate degree such as DVM, PharmD, PhD, MSN with advanced clinical specialty (Clinical Nurse Specialist/ Nurse Practitioner) and one of following:

• 3-5 years of clinical experience, ideally in the area of oncology/hematology, or
• 3-5 years of pharmaceutical experience (2 of which is in clinical development)

OR

• University degree/ Master-degree or PhD in medicine, pharmacy, life science, or health economics that is directly related to at least one of the following:

• Clinical trial experience
• Experience in areas relevant to drug discovery
• Drug/clinical development experience (for example, epidemiology, toxicology, pharmacology, regulatory affairs, medical affairs)

What do we also expect?

• You are familiar with MS Office (Word, PPT, Excel, etc.), Outlook, MS Teams.
• You are fluent in English and German, with a good command of French, verbal and written communication.
• You are goal and solution oriented and have a passion for teamwork.
• You enjoy working in a fast-paced and challenging but fun environment.
• You have the ability to move work forward, even in the face of ambiguity.

Engagement in domestic and international travel to the degree appropriate to support the business of the team will be required. Travel requirement is expected 40% of time.

Eli Lilly (Suisse) SA is based in Geneva. For an applicant living in the German part of Switzerland, consider the possibility of working partially remotely.

Contract subject to a valid work permit in Switzerland.

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. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

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.

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