- The selected interns will work with assigned mentors on projects to help improve leadership, problem solving, and critical thinking skills
- Experience different disease-therapeutic areas, and associated regulatory areas including Product Labeling, Chemistry, Manufacturing and Controls, Policy and Intelligence
- Work with knowledgeable mentors and develop skills to build a strong career foundation
- Work on programs and strategies for compounds in development and/or marketed products
- Use creative problem-solving skillsets, to develop new ideas and insights, including takeaways about yourself as a leader
- Interns will be assigned to projects to help and support the regulatory leads and will be required to manage their time appropriately without major supervision.
- The interns will be required to make a final presentation in terms of their learnings from the program and may be asked to provide recommendation about the improvement needed for the future interns.
- The intern will be provided a topic that is related to global regulatory issues/challenges with the help of their individual mentors.
- The intern will participatein certain department activities and initiatives related to the project.
- Currently enrolled full-time and have completed at least 3 years in an undergraduate program, or enrolled full-time in a graduate program, pursuing a degree majoring in a scientific, technology, pharmacy or engineering related field
- Examples include, pharmacy, biomedical engineering and other biological other healthcare science
- Pharm D Students that are currently enrolled in P2 and P3 along with those that are enrolled in masters degree from an accredited DRA Program are also encouraged to apply.
- Possess a can-do approach, and courage to speak your voice and suggest innovative ideas
- Detail-oriented, highlymotivated, able to manage multiple tasks and to work independently and as a team member.
- Students with demonstrated leadership skills in projects at home and abroad will be preferred.
- Good communication skills are a must.
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Global Regulatory Affairs Intern - Bernards, United States - Daiichi Sankyo
Description
Join a Legacy of Innovation 110 Years and Counting
Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class scienceand technology. With more than 100 years of scientific expertise and a presence in more than 20 countries, Daiichi Sankyo and its 15,000 employees around the world draw upon a rich legacy of innovation and a robust pipeline of promising new medicines to help people. Under the Groups 2025 Vision to become a Global Pharma Innovator with Competitive Advantage in Oncology, Daiichi Sankyo is primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders.
Job Summary:
We are currently seeking a Regulatory Affairs Strategy Intern. This full time time position works for approximately 37.5 hours per week for the summer. The candidate will work closely with and report to the Regulatory Affairs Leadership team and will gain experience in the RA life cycle process. Basic responsibilities include:
Qualifications:Successful candidates will be able to meet the qualifications below.
Education/Experience:
Daiichi Sankyo, Inc. is an equal opportunity/affirmative action employer. Qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law.
