Graduate Intern - Global Regulatory Policy & Intelligence

Gilead Sciences

Sep 28, 2023

Applications are closed

Internship
Full-time
Off-cycle Internship
Business, Operations & Strategy
San Francisco

Requirements

Required Qualifications:
Must be at least 18 years old
Must have a minimum GPA of 2.8
Authorized to work in the United States without Sponsorship now or in the future or CPT/OPT through your University.
Must be currently enrolled as a full-time student in a Masters/MBA/PhD program at an accredited US based university or college
Must be a Rising Sophomore, Junior, or Senior in undergrad or a Graduate or Doctoral Student
Must be enrolled full-time in the Fall Semester at an accredited university/college after the completion of the internship
Must be able to complete a 10-12 consecutive week internship between May and August
Must be able to relocate if necessary and work at the designated site for the duration of the internship
Preferred Qualifications:
Proficiency with MS Office Suite
Ability to identify issues and seek solutions
Ability to work both independently and collaboratively
Demonstrated commitment to inclusion and diversity in the workplace
Efficient, organized, and able to handle short timelines in a fast-paced environment

Responsibilities

Oncology Products Policy Research (75%):
Research novel and innovative oncology approaches topics like Contribution of Components for PDL1 Combination Strategies, methods for validating for novel endpoints, and investigation of biomarkers
Practice writing science-based articles for regulatory agencies review, consideration, and presentation.
Regulatory Intelligence Project (25%):
The research project will assess the impact of a US Food and Drug Administration (FDA), European Medicines Agency (EMA) or the International Council for Harmonization (ICH guidelines) impacting the Gilead oncology portfolio.
Research will be conducted using quantitative and qualitative analyses.
Other Professional Development Opportunities:
Outside of the Project, other professional development opportunities will be presented.
Partner and collaborate with the Development, International Regulatory affairs, and other cross functional stakeholders to understand research priority.
Conduct background research related FDA, EMA and ICH guidelines or other data need identified to support Gilead non cell therapy oncology pipeline products
Identify potential areas where guidance clarity is necessary, outdated or new references may be forthcoming
Partake in the development of research methodology and project plan; through contributing relevant research
Compile and analyze relevant qualitative and quantitative data
Present findings in a deliverable of professional quality and presentation to the broader team; and
Potential submission of the project, in article form, to Professional Societies, journals or at conferences.
Showcase your work with a final poster board presentation near the conclusion of your internship

Gilead Sciences

Science & Healthcare

Industry

10,001+

Employees

1987

Founded Year

Mission & Purpose

The way we see it, the impossible is not impossible. It’s simply what hasn’t been achieved yet. For more than 30 years, we’ve pursued it, chased it down, tackled it for answers and surrounded it for a way in. We have worked tirelessly to bring forward medicines for life-threatening diseases. Creating Possible drives everything we do. It’s evident in our mission and core values. This is how we built a culture of excellence that is fueled by a passion for improving lives of people around the world. For us, nothing is impossible – because of the people we work with, the communities we stand with and the partners we push forward with. Our ~12,000 employees band together through science, grit, compassion and courage to prove the impossible wrong. At Gilead, the tangible results of your contributions are evident. Where every individual matters. Where all employees can enhance their skills through ongoing development. And where we start every day with one question: “What’s next?”