As a Senior Medical Expert (m/f/d): Real World Evidence, you will be responsible for the development of integrated evidence generation, the implementation of RWE projects and for deriving recommendations to internal stakeholders. In this key position, you will play a crucial role in focusing on the unmet needs of our patients and ensuring the realization of our philosophy “Better outcomes for more patients”.
YOUR CONTRIBUTION
Integrated Evidence Planning: Create an IEP (integrated evidence plan) and study designs along the product life cycle to generate scientific evidence and act as a project manager for outsourcing during study conduct
Real World Data: Analyze real-world data (RWD) and create evidence-based reports and use the insights for your strategic suggestions.
Patient centricity: Ensure that all studies are conducted ethically and patient safety is guaranteed. Taking opinions and needs of patients into account when planning studies in order to work towards our common goal of “Better outcomes for more patients”
Advisory Boards: Implementation and planning of advisory boards with HCP, patients and payors to inform study design; ensure compliance with GxP guidelines and regulatory requirements for RWE studies
Crossfunctional Approach: Engage in crossfunctional teams (Market Access, Marketing, GPT, R&D and digital hub) and represent your department in result-oriented project teams
Organizational and Process Development: Work in accordance with SOPs, complications, policies & procedures and systems to support all Medical Affairs operations
Strategic Communication: Strong thought leader relationships for physician messaging via robust podium presence and medical literature. Ability to guide agencies through effective writing process
IIT: Align and execute IIT strategy, as well as results communication to internal stakeholders
YOUR PROFILE
Medical or scientific university degree in Biology, Biochemistry or Pharmacy (MD, PhD). Therapeutic area (neurology, rehabilitation) experience is a plus.
Relevant experience in pharmaceutical industry, with track record of successful RWE strategy and execution
Experience in planning, interpretation and publication of clinical studies with innovative and/or digital design
Strong project management skills, ideally familiar with agile working methods
Fluent in English, German ideally at least basic conversational
Strong team-working and communication skills, able to understand and communicate complex science
Reliable and authentic personality who can gather a team towards our common goal
YOUR BENEFITS
Find out more about our benefits here.
ABOUT US
Welcome to Merz Therapeutics, a leading pharmaceutical company that helps people with movement disorders, neurological diseases, liver diseases and other health conditions regain their quality of life.
We are proud to be a family-owned and value-driven company that has been dedicated to serving the needs of our patients for 110 years and is now a global innovation leader with products in more than 90 countries.
Our goal is to use our products to improve treatment outcomes for patients around the world, thereby reducing the burden of suffering for affected people and their surroundings.
Our dedication and commitment to relentless research and development is to ensure that unmet patient needs are identified and appropriate treatments are provided.
Therefore, become part of our international and motivated Merz Therapeutics family now and help us achieve our goal:
"BETTER OUTCOMES FOR MORE PATIENTS"