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The Medical Value Partner (MVP) provides field-based resources for the assigned therapeutic  areas , for the medical organisation, in the context of their work, in accordance with local news, regulations and codes, as well as Roche SOPs.

Key responsibilities

Identifying and addressing the relevant medical information needs of clinical practice, in the context of his/her work, in accordance with local news, regulations and codes, as well as Roche SOPs ,to successfully support the optimal use of Roche products.

Acts as a guardian for high standards of compliance, ethics, and safety of Roche products, putting patients at the center of his/her actions.Makes the mapping and feasibilities for the assigned TA(s) / TA(s) on focus

Generates insights from the field and bring them back into the Medical organization; also supports medical training needs of Marketing and Commercial organizations

Contributes to the tactical/field Medical plans; 

Maintains up-to-date information/education on latest scientific data and topics (e.g. new pathways, mode of action (MoA), new assays/compounds);

Looks for opportunities for scientific and educational collaboration, including the organization of advisory boards;

Identifies, collects and immediately reports all safety and or product complaint related information on Roche products, according to company procedures and local regulatory requirements.

Monitors and provides competitor activities regarding medical trends and topics

Ensures approval of all promotional activities and materials in the specific therapeutic area in line with Roche and local legal requirements. 

Links affiliate to Therapeutic Area and Product(s) Communities (as Roche Currents), to deliver on data generation, knowledge exchange/data communications.

Ensuring that all enquiries related to designated Roche Products received from all sources (e.g. via phone; e-mail; letter; fax; face to face) are resolved to the required standard;

Identifies, collects and reports any adverse event (AE) and/or other reportable event (PRI or PSI) and forward to appropriate department within timelines described in relevant SOPs;

Assures compliance with Roche Global and Local MI Directives/SOPs and local regulations;

Who you are:

Advanced knowledge of English (both written and spoken) and of MS Office suite.

Driving license B mandatory and availability to travel.

Strong time management skills: can prioritise multiple tasks and goals to ensure timely and high-quality accomplishment.

Able to build and cultivate relationships with key partners/stakeholders and to work effectively in cross functional teams.

Highly motivated self-starter who takes initiative with minimal supervision and works independently in a team-oriented environment.

Knowledge in interpreting the scientific medical data (statistics) and protocol design would represent an advantage,

Strong project management skills including planning, documenting, communicating and delivering the end-result on-time and within budget would represent an advantage.

Strong analytical, problem solving and decision making skills to evaluate alternatives and provide recommendations on business issues.

You have a University degree – Medical Doctor, Pharmacist or licensed in any medical related science area

You have at least 2 years of medical practice or in a similar role in the health industry.

At Roche, more than 100,000 people across 100 countries are pushing back the frontiers of healthcare. Working together, we’ve become one of the world’s leading research-focused healthcare groups. Our success is built on innovation, curiosity and diversity.

Roche is an Equal Opportunity Employer.