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Intern, International Regulatory Affairs

72% Flex
UNLIMITED HOLIDAYS - EXTRA HOLIDAYS - EXTRA PARENTAL LEAVE - LONG REMOTE PERIOD ALLOWED
Remote: 
Full Remote
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Offer summary

Qualifications:

Currently enrolled or recent completion of Bachelors/Masters degree in life science, pharmacy, pharmaceutical sciences, or chemistry.

Key responsabilities:

  • Gain exposure to international regulatory affairs and market access
  • Participate in marketing applications & complex market access processes
  • Craft projects based on interest & business needs
Blueprint Medicines logo
Blueprint Medicines Biotech: Biology + Technology SME https://www.blueprintmedicines.com/
501 - 1000 Employees
See more Blueprint Medicines offers

Job description

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Your missions

Title: Intern, International Regulatory Affairs

Manager: Nabila Nazir & Ning Lu

Location: Zug, Switzerland

 

Blueprint Medicines is a global precision therapy company that invents life-changing therapies for people with cancer and blood disorders. Applying an approach that is both precise and agile, we create medicines that selectively target genetic drivers, with the goal of staying one step ahead across stages of disease. Since 2011, we have leveraged our research platform, including expertise in molecular targeting and world-class drug design capabilities, to rapidly and reproducibly translate science into a broad pipeline of precision therapies. Today, we are delivering approved medicines directly to patients in the United States and Europe, and we are globally advancing multiple programs for systemic mastocytosis, lung cancer and other genomically defined cancers, and cancer immunotherapy. For more information, visit www.BlueprintMedicines.com and follow us on Twitter (@BlueprintMeds) and LinkedIn.

 

Responsibilities:

This 9-month internship (full-time or 4 days per week) will serve as an introduction to International Regulatory Affairs and Market Access.  This is a fantastic opportunity for students who have just finished their university cycle or who are still enrolled in a university degree program to gain exposure to these two crucial functions in an International start-up biotech environment.  Within Regulatory Affairs, you will gain first-hand exposure to the registration process of international submissions being exposed to marketing applications and helping with other lifecycle management activities.   Within Market Access, you will gain exposure to the complex process of obtaining market access and reimbursement and to the health technology assessment.   The internship will start on September 1st.

Projects will be crafted along one or multiple of the following key areas based on interest and business needs:

Regulatory Affairs:

  • Be involved/exposed to a marketing application and the submission/preparation process
  • Shadowing the International Regulatory Affairs team in order to understand various aspects of the regulatory process
  • Participate in Global Regulatory Sciences (GRS) 2024/2025 Project Improvements
  • At completion of internship present an overview at a GRS department meeting

Market Access:

  • Shadowing the International Pricing & Market Access team to gain understanding of the complex market access and pricing process
  • Conduct secondary research on healthcare system and healthcare policy, e.g. EUnetHTA and Joint Clinical Assessment and present to the International Pricing & Market Access team

 

On-site Expectations:

While blueprint offers flexibility to work from home, you will gain the most of this experience by being on-site and learning first-hand from the key functional stakeholders.  For this reason, we request presence in the office at least twice per week, to be agreed with respective functional managers. 

 

Qualifications:

SCHOOL YEAR: You are currently enrolled in a Bachelors or Masters degree or you have just completed your Bachelors or Masters degree

  • MAJOR OR AREA OF STUDY: Life science related disciplines (e.g. Biology, Biochemistry, Molecular Biology etc.), Pharmacy, Pharmaceutical Sciences or Chemistry
  • BROAD AREAS OF INTEREST: Market Access, health technology assessment, healthcare systems, Regulatory Affairs, drug development and lifecycle management

 

WHO WE ARE:

Blueprint Medicines’ mission is to dramatically improve the lives of patients with genomically defined diseases. Our singular focus is to use our deep understanding of the genetic blueprint of cancer and other diseases driven by the abnormal activation of kinases to craft highly selective medicines aimed at eradicating these diseases.

We don’t think in small steps. We think in giant leaps.

We are driven by the pursuit of new ideas, new innovations, and new ways of thinking.

We know that what each and every one of us does matters and that our success depends on our ability to work together. We believe we are at our best as a company when our employees are thriving and foster a culture that provides opportunities to grow and develop professionally, while also having fun.

Required profile

Experience

Industry :
Biotech: Biology + Technology
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Soft Skills

  • Proactive Mindset
  • Excellent Communication

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