PRA Manager Denmark
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 35,000 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.
Pricing, Reimbursement and Access (PRA) Manager, Denmark
Lilly is a global healthcare leader that unites caring with discovery to make life better for people around the world. We were founded more than a century ago by a man committed to creating high-quality medicines that meet real needs, and today we remain true to that mission in all our work. Across the globe, Lilly employees work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to communities through philanthropy and volunteerism.
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. The greatest measure of our diversity efforts is our ability to attract and retain exceptional employees who feel comfortable in a culture that supports them being themselves.
Join Lilly, who has been recognised as one of the world’s most ethical companies for 5 straight years in a row. We have a fantastic opportunity to join our Northern European Hub team of PRA Managers, based in Denmark.
We’re looking for you to manage and help deliver Lilly product access dossiers to the Danish Medical Counsel (MC). You’ll lead Market Access initiatives across the 5 Danish regions including the work on guidelines and recommendation lists, and maximise sales/positioning in national tender process. This role encompasses the project management of Lilly submissions to ensure delivery by the deadline and becoming a technical expert on MC submission processes, working across therapeutic areas with other members of the PRA team and various internal stakeholders to ensure the best probability of success with the MC body in Denmark. We’ll need you to bring your understanding of complex/detailed clinical data to write or contract out clinical sections of submission and drafting responses to MC during the process. In addition, this role will also cover Market Access related activities across regions and Lilly’s portfolio.
Some of your key responsibilities:
- To develop a project plan for each submission and ensure that all the required company inputs are delivered on time.
- Manage relationships with selected vendors to deliver submission on time and to budget.
- To organise and chair kick-off meetings and meetings with internal stakeholders
- Manage internal stakeholder list (brand, region and global) and ensure all relevant personnel are consulted at the appropriate time.
- To influence internal and external customers through personal credibility
- To maximise opportunity for all brands by ensuring payer strategy is aligned with business objectives.
- Apply environmental knowledge and bring the outside in to inform pathways and to anticipate and understand future customer needs.
- Support development of value propositions and payer objectives for selected brands
- Lead PRA aspects of customer planning process for selected brands.
- Follow tender best practices including environmental shaping
- Develop business cases for pricing committee
You come to us with these required skills:
Pharmacy or Life science degree
Previous experience of Market Access and writing submissions
Experience in medical, drug surveillance, regulatory activities or allied area
Experience of developing high quality technical documentation for external agencies
Attention to detail
Strong interpersonal & communication skills
Strong project management skills, great team worker attributes
Confidence and willingness to take on new challenges and manage multiple projects
Self starter and lot of drive
Good Knowledge of Danish Medical Counsel.
Skilled in using data analytics as part of the decision making
High level of English, both written and verbal
Previous Danish Medical Council or industry experience
Worked in multiple therapy areas, in particular Rheumatology and Dermatology.
Exposure to, or experience in multichannel engagement practices.
This role can be based anywhere in Denmark.
Sound like you? With a pipeline and career at Lilly this promising, there has never been a better time to join the Lilly family!
Eli Lilly and Company, Lilly USA, LLC and our wholly owned subsidiaries (collectively “Lilly”) are committed to help individuals with disabilities to participate in the workforce and ensure equal opportunity to compete for jobs. If you require an accommodation to submit a resume for positions at Lilly, please email Lilly Human Resources ( Lilly_Recruiting_Compliance@lists.lilly.com ) for further assistance. Please note This email address is intended for use only to request an accommodation as part of the application process. 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.
To submit resume, visit https://www.lilly.com/careers and apply to Req ID R-16500.
Lilly is an EEO/Affirmative Action Employer and 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.
Our scientists and researchers are developing the breakthrough medicines of tomorrow. Join us and become a creative innovator and thinker who can improve the lives of millions.
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