Schweiz, Basel-Stadt, Basel
enfresrutritptzhja
Apply now!PrintAt Roche, we believe it’s urgent to deliver medical solutions right now – even as we develop innovations for the future. We are passionate about transforming patients’ lives and we are courageous in both decision and action. And we believe that good business means a better world.
That is why we come to work each day. We commit ourselves to scientific rigour, unassailable ethics, and access to medical innovations for all. We do this today to build a better tomorrow.
The position:
Working across Pharma International enables PEP network to drive ecosystem and organizational readiness for pivotal data-release
Ensures quality input into medical/scientific planning, including local data generation, scientific collaboration and knowledge exchange activities, in line with global strategy
Ensures alignment and communication with other stakeholders including RED’s, PD and Roche Diagnostics when applicable on all matters related to planning medical activities
Contributes to establishing and implementing appropriate policies and standards
Collaborates with respective I8, I7 and HQ partners to define regulatory and access data gaps and develop tailored market access and regulatory strategies
Collaborates with RC Enabling office, PEP network, medical affairs and regulatory to identify options for acceleration of approvals by co-creation
Acts as reference for data generation activities
As the Disease Area Medical Director for Rare Conditions you will have the following accountabilities:
Provide scientific support to the PEP network and ecosystem
Guide and advise PEP network, ensuring alignment with global disease area strategies, plans and objectives
Establish and maintain relationships with internal stakeholders including but not limited to RED, PD, DIA contributing to medical strategies and exchange of medical insights
Establish and maintain relationships with scientific advocacy organizations and through leaders
Contribute to onboarding and PEP network learning and development programs
Support integrated evidence generation strategies, as appropriate support the design and development of clinical studies
Ensure medical compliance of PEP/ecosystem generated activities
Act as an internal and external ambassador for the RC model and continuous learning
Who you are:
You have professional disease area experience, in clinical practice and in the pharmaceutical industry (typically min 6-8 years, preferably in medical functions)
Profound experience in pharmaceutical medicine incl. data generation, medical communication, medical information, regulatory processes and pharmacovigilance
MD with relevant clinical experience (patient care decision-making) at the point of care and board-certified specialist in the respective disease area
Track record of making decisions and aligning the organization behind them
Experience partnering with TAEs and external organizations
You demonstrate the following skills and abilities:
Broad understanding of business context, including access evidence requirements and external value / decision making drivers
Proven expertise with a wide range of data and information analysis and synthesis
Profound knowledge of the overall drug development process
Strong knowledge of medical compliance and relevant regulations (e.g. ICH GCP, GPP, PV)
Strategic Agility & Managing Change - you demonstrate critical thinking and flexibility to overcome unfamiliar challenges
Teamwork, Collaboration and ability to work across multiple cultures and countries
Inspiring and Influencing - you can influence without authority and has proven experience building and cultivating relationships with key partners and stakeholders, both internally and externally.
Has demonstrated Roche Values, leadership commitments & core competencies to a consistently high level
Are you ready to apply? We are looking for someone who thinks beyond the job offered - someone who knows that this position can be a rare springboard to many other opportunities at Roche.