Major Responsibilities

- Provide insight and recommended actions that support the highest value proposition for the pipeline products and/or new indications.

- Identify and address the relevant medical needs of clinical practice, to support the pre-launch phase of Roche pipeline products.

- Actively engage with Internal and External stakeholders to inform and shape public policies and ecosystem for upcoming Roche Pipeline products within new therapeutic areas.

- Link affiliate to Global Medical Affairs objectives and CT/IMT/DST strategy to deliver on data generation, knowledge exchange / data communications, and to lead TAE engagement in a scientific manner.

- Develop effective interactions with Clinical Operations (PDG, PDMA and PA), including but not limited to placing studies, provide input on feasibility, sites and investigators selection for all Roche pipeline products.

- Provide early insights on new products and indications in close collaboration with the PDG group.

- As the affiliate RWD Lead/back up, liaise with global teams all locally initiated RWD Initiatives and bringing to the affiliate any applicable global RWD solutions/initiatives that can be utilized locally.

- Train, where applicable, teams on RWD solutions that are relevant to their disease area.

- Support local teams with importing relevant RWD solutions to support their local Ecosystem needs.

- Leverage external and internal stakeholder inputs/partner with key stakeholders to identify data generation Gaps

- IIS/NIS local representative/back up & Publication Lead/back up

- Support Real World Evidence generation efforts and oversee the phase III-B/IV trial program by holding effective relationship with the Clinical Operations team and Ecosystem stakeholders.

- Inform other Affiliate functions on Global planned studies

- Medical expertise and customer insights to the Patient Journey Partners, Healthcare System Partners and Ecosystem Enablers.

- TAE engagement plan to support medical objectives: identification, development, and establishment of scientific relationship with TAEs

- Support for Pharmacovigilance activities, including assurance of appropriate adverse event reporting in coordination with LSR

Desired Candidate Profile

Who you are

Required Education and Experience

- Bachelor degree in Medicine/Pharmacy, additional business degree would be an advantage

- Fluency in English written and verbal & Arabic

- Professional experience within the pharmaceutical industry

- Experience in TAE relationship management

- Experience in the principles and techniques of data analysis, interpretation, and clinical relevance

- Knowledge of the overall drug development process relevant to pharmaceutical/biotechnology organizations processes

- Experience in preparation and delivery of scientific program (preferred)

- Familiar with code of conduct and Pharma regulations

Required Competencies and Skills

- Combines forward-looking vision with strong problem-solving capabilities to address complex challenges and drive sound decision-making.

- Delivers disciplined end-to-end execution, meticulous planning, and strong organizational skills to manage deliverables with initiative.

- Drives lateral leadership and team development through targeted coaching, mentoring, and the ability to influence without formal authority.

- Champions organizational change, navigates ambiguity, and resolves interpersonal and operational conflicts with resilience.

- Leverages solid data analysis capabilities to interpret complex metrics, identify patterns, and guide evidence-based actions.

- Demonstrates strong interpersonal presence, clear presentation delivery, and persuasive storytelling tailored to diverse audiences.

- Builds impactful internal and external networks across cross-functional, multicultural matrix environments to partner seamlessly with commercial counterparts.