Real World Evidence

vor 2 Wochen


Zurich, Schweiz MSD Vollzeit

We are a research-driven biopharmaceutical company. Our mission is built on the simple premise that if we “follow the science” and that great medicines can make a significant impact to our world. And we believe that a research-driven enterprise dedicated to world-class science can succeed by inventing medicine and vaccine innovations that make a difference for patients across the globe.

**Role Summary**
- This role sits within the Local Data Generation Center of Excellence (LDG COE) within Global Medical and Value Capabilities (GMVC) organization in Global Medical and Scientific Affairs (GMSA)
- This individual is primarily responsible for providing methodological and scientific support for the design, analysis, study reporting and publication development of non-interventional research studies

**Responsibilities and Primary Activities**
- Facilitates the development and execution of high-quality, consistent, and methodically sound scientific study protocols for approved Local Data Generation (LDG) study concepts in collaboration with the study lead and colleagues across Global Medical Scientific Affairs and Center for Observational and Real-World Evidence (CORE):

- Develops clear and concise study protocols, statistical analysis plans, and study reports for a diverse range of studies and activities in compliance with Good Pharmacoepidemiology Practice (GPP), along with Research Laboratories and CORE standard operating procedures (including primary/secondary data collection, chart review, database, registries, molecular epidemiology studies, literature reviews, dossier development and economic modeling support)
- Provides centralized, above therapeutic area, scientific direction for data collection and statistical analysis plan development for assigned studies
- Identifies and develops methodologies and strategies in partnership with study leads and project teams
- Provides scientific writing support to study lead for abstract/poster presentations at international/national congresses and publication of articles in scientific journals for assigned studies
- Harmonizes and facilitates scientific learning and experience across different study types and across countries
- Develops and maintains a knowledge repository of regional/local vendors used for LDGs and their capabilities
- Facilitates training on Non-Interventional Studies (NIS) methodology by identifying knowledge gaps and translating them into training modules for LDG study leads
- Maintains awareness of scientific developments, both in terms of new methodology and new activities to establish communications with key outcomes research opinion leaders
- Actively participates in internal process improvement initiatives or other operational projects (including leading some initiatives) to support GMVC leadership and team member mentorship

**Required** **Qualifications, Skills, & Experience**

**Minimum**
- Master’s degree from a school of medicine, public health, management, pharmacy, or economics

**and**
- Minimum of 3-5 years of experience in the design and implementation of non-interventional, RWE, epidemiological, or health economic studies within the pharmaceutical industry, Contract Research Organization (CRO) or academia
- Excellent leadership and strategic thinking skills
- A track record of scientific presentations and publications
- Excellent communication and interpersonal skills and the ability to collaborate with and influence a wide variety of stakeholders
- Strong project management and prioritization skills
- A high level of motivation and the ability to work independently and collaboratively

**Preferred**
- Doctoral degree from a recognized school of medicine, public health, management, pharmacy, or economics
- Demonstrated expertise in the field of outcomes research, epidemiology, or health economics

**COMPANY**

Our company has had a presence in Switzerland since 1963. With a regional office and manufacturing/packaging facility, Lucerne is considered the center of operations. Approximately 1,000 people work collaboratively at the four Lucerne locations (Tribschenstrasse, Citybay, Schachen and Kriens). A fifth location has been recently established in Zurich, aimed at accelerating the development and commercialization of many of our company’s medicines and vaccines, which supports our mission to save and improve lives around the world. The new location has a target date of 2021 for operational readiness.

We are proud to be certified as a “Top Employer Switzerland” and “Top Employer Europe” showing the company’s commitment to our employees and the community around us.

The Switzerland Head Office of our company’s Swiss Subsidiary is based in Lucerne's city centre. Located in the heart of the city, employees work collaboratively across many departments including commercial, market access, medical affairs, clinical research, regulatory affairs, and policy & communications.

**WHO WE ARE **

We are known as Merck &


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