At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.

The Position

Medical Lead is the key Medical Affairs role that develops broad medical & scientific expertise within the given Disease/Therapeutic Areas. As a Medical Lead, you support the development and execution of patient-focused medical strategies and primarily drive scientific exchange and evidence generation activities.

Key Responsibilities

You are a strategic partner who provides medical insights and expertise to the organisation and executes all planned medical activities.
You will be the medical responsible of the team and will be more in the field.
You manage the integrity and accuracy of scientific and medical data communicated internally and externally for promotional and non-promotional purposes.
You collaborate with stakeholders in identifying and prioritising relevant research ideas and developing them into research projects.
You collaborate closely with Clinical Operations across different phases of interventional clinical trials: Gaining clarity and communicating/spreading the knowledge to communities of interest, helping to define and maintain country participation strategy, supporting development of sites selection strategy through a disease area lens by different means including participation in site feasibility activities, pre-activation site visits and other F2F and remote interactions with the sites as needed, patient recruitment & retention, protocol & patient-related issues, scientific communication of study results, clinical study report and scientific publications.
You detect the medical gap/need for RWD/E generation activities by reviewing Integrated Evidence Plans, communicate, agree and document, plan & execute and/or participate in respective work in non-interventional studies and RWD/E generation activities: Definition of the research questions and study objectives, study design and protocol, study budget, feasibility, site selection, pre-activation and ad-hoc visits, patient recruitment, protocol & patient issues, scientific communication of study results, clinical study report and scientific publications.

Who You Are

You have a Medicine, Pharmacy, or Dentistry degree
Your experience in Oncology (Lung) is preferred
You have previous experience in the Pharma Industry
You are fluent in Turkish and English
You have strategic thinking and a growth mindset
You are collaborative and experienced in stakeholder management

Who we are

A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.

Let’s build a healthier future, together.

Roche is an Equal Opportunity Employer.