Intern Co-op, Global Value & Access

This application is for a 6-month student role from July - December 2025. Resume review begins in Feb 2024.This co-op position will be part of the global litifilimab team at Biogen. This is an exciting opportunity to gain hands-on experience in real world evidence generation and its application to research, medical and commercial issues and ensure that Biogen medicines are developed in line with the business strategy.

Projects may include analyzing clinical and economic data and coordinating complex projects under the guidance of experienced professionals and subject matter experts who are invested in your career and academic growth.

There are a number of opportunities to build your network, learn more about the organization through weekly lunch and learns led by leaders from across the company, in addition to several fun events for interns.

Collaborating with other teams will give the successful candidate a range of insights into the roles within a pharmaceutical company.

Position Description

This position will be part of the Global Value & Access team. The primary responsibility of the co-op is to support project lead in plan, design and execution of Real World Evidence (RWE) studies to develop and demonstrate the value of Biogen’s pipeline assets to scientific, clinical and payer stakeholders.

Who You Are

You enjoy working in a highly matrixed / cross functional global research environment.

You have good training on RWE studies such as writing protocols, conducting literature searches, writing draft analysis plans, and programming.

You have an interest in using real-world evidence (RWE) data sources (e.g., claims, EHR, registries) to support launch readiness and demonstrating product value over the product’s lifecycle.

To participate in the Biogen Internship Program, students must meet the following eligibility criteria:

• Legal authorization to work in the U.S.
• At least 18 years of age prior to the scheduled start date
• Be currently enrolled in an accredited community college, college or university

Additional qualifications:

• Minimum of 2-3 years of experience using Real World Data sources in healthcare.
• Demonstrated knowledge of existing databases, strengths and weaknesses, inherent coding systems such as ICD-9/ICD-10, NDC, CPT, HCPCS etc.
• Proficiency in conducting targeted literature reviews and landscape assessment to inform decision-making.
• Expertise in study design using a variety of Real World Data sources (such as claims, EMRs, registry data etc.) for research purposes.
• Good understanding of statistical methodologies commonly used in analyzing Real World Data sources and ability to write high-quality study protocols/SAPs.
• Strong programming skills in SAS and/or R are required.
• Demonstrated ability to effectively communicate complex information.
• Excellent team work.
• Proactivity and willingness to learn.
• Excellent time management and attention to detail.
• Ability to work independently.
• Excellent interpersonal skills.

Education

Advanced degree (PhD or Masters) students in epidemiology, public health, HEOR, biostatistics or related field. Advanced PhD students past qualifying exams are preferred.

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