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Medical Science Partner Neuroscience

Role purpose

Leads the development and is accountable for implementation of the medical part of dedicated Therapeutic Areas (TA) strategy that ensures better outcomes for patients by being timely diagnosed and treated, gaining preference from our stakeholders, accelerating access through customer centricity, bringing a holistic product strategy across organization.
Reports to Country Medical Director

Responsibilities

Responsibility for local adaptation of global medical strategy, for preparation and realizations medical tactics  in frame of  dedicated therapeutic areas

Ensuring strategic close collaboration with key clinical experts (being PPOC for key clinical experts), providing them with regular medical scientific updates in dedicated  therapeutic areas  (TAs)

Ensuring scientific support for PPOCs in frame of dedicated TAs for registered and unregistered treatment and diagnostic solutions

Member of launch readiness team, contribution to launch readiness strategy and pre-launch activities in frame of dedicated  TAs in order to achieve effective launch and prepare disease area to new products.

Developing meaningful alliances with different stakeholders within the country ecosystems, insights collection, accelerating access and improving customer experience and patient outcomes, ensuring sustainability while improving company reputation and strengthen value relationships

Leverage data and insights to build positive experiences for our customers by understanding their needs and insights, resulting in customer satisfaction and improved patient journey to our innovation

Preparation local and adaptation globally available non-promotional materials in dedicated TAs

Contribution to preparation and realization omnichannel strategy in dedicated TAs

Work in the related Company systems (Veeva VPM, EpicX, etc) in accordance with internal and external regulation

Contribution\\support in frame of  dedicated TAs for regulatory\\safety activities

Contribution\\support in frame of dedicated TAs for access dossiers preparation

Accountable for collecting evidence gaps and related needs in dedicated TAs and ensure relevant RWD/E availability and collection if needed.

Leading RWD activities and IIS in frame of  dedicated TAs 

Local Coordinator for patients early access programs (CUP\\PAA) and PTA (if it will be required)

Working collaboratively and sharing expertise across the organization to remove silos and duplication, ensure efficient use of similar skill-sets, and to ultimately support common pursuit of the North Star.

Involvement in Affiliate Team work, Network and Global activities, as required

Compliance with relevant internal standard operation procedures and external regulation

​Critical capabilities

Clinical Expertise in dedicated  therapeutic areas

Relevant experience in pharm industry is additional plus

Environmental expertise (patient journey, healthcare system landscape, etc.)

Analytic, strategic and agile thinking (being & doing)

Growth mindset

Innovative/ creative thinking  

Strong communication skills

Collaborative, team-worker, able to focus and prioritize, outcome oriented

Fluent English (both verbal and writing)

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.