At 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 confident 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.
As an Associate Medical Director you will:
- Participate in Clinical Development strategy development and present to various internal committees,
- Provide clinical oversight across all relevant studies and programs,
- Lead and/or otherwise participate in ongoing clinical study team and relevant sub-team meetings, other interactions and communications,
- Work with regulatory and other internal partners/stakeholders in the completion and submission of regulatory filings and other regulatory documentation. Support others with clinical science information and input for regulatory submissions and other regulatory processes. Includes developing labeling and packaging language, etc.
- Play a lead role in the development and implementation of communication strategies to support existing and concluded studies. Includes Key Opinion Leader (KOL) interactions, advisory boards, major medical meetings, congresses and other events, publications and other materials
- Contribute clinical science input into the relevant therapeutic/disease area scientific strategy,
- Help research and other Product Development groups to ensure consistency of scientific and late-development strategies with target label claims and corporate clinical development goals,
- Collaborate with a variety of internal and external organizations and partners, such as clinical investigators, clinicians, scientists and key opinion leaders (KOLs), as well as multidisciplinary internal groups, including other groups in Product Development, research, business development, commercial operations, legal, etc.
Who you are:
You’re someone who wants to influence your own development. You’re looking for a company where you have the opportunity to pursue your interests across functions and geographies.
Where a job title is not considered the final definition of who you are, but the starting point.
We are looking for a professional with 2+ years of drug development experience in the biotechnology or pharmaceutical industry or a combination of academia and industry (industry is a nice to have, but we are open) and with experience in the design, conduct, analysis, and reporting of clinical studies.
In addition, you bring:
- M.D. degree with board certification or eligibility in Oncology or Hematology/Oncology
- Solid tumor experience, preferably in breast cancer, expertise and an interest, preferably experience, in Cancer Immunotherapy experience
- Exposure to next-generation engineered molecules and doublet and triplet combination study clinical trials (both are of advantage)
- Significant successful interactions with key opinion leaders and investigators globally
- An excellent scientific track record proven by publication record in peer-reviewed journals
Are you ready to apply? We want someone who thinks beyond the job offered - someone who knows that this position can be a rare springboard to many other opportunities at Roche.
Roche embraces diversity and equal opportunity in a serious way. We are committed to building a team that represents a variety of backgrounds, perspectives, and skills. The more inclusive we are, the better our work will be.
Please note that this position can be based in the UK (Welwyn) and we will accept applications only until the 23rd of February 2019.