Intern – Benefit Risk Sciences Established Products (BRSEP)

For Current Gilead Employees and Contractors:

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At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world’s biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.
 

Every member of Gilead’s team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we’re looking for the next wave of passionate and ambitious people ready to make a direct impact.
 

We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together.

Job Description
 

As a Gilead intern you will contribute to high-impact meaningful projects that will not only further advance our company’s mission but will allow you to gain real world experience at one of the most innovative organizations in the world.  You will also have opportunities to participate in special events including professional development and leadership presentations, social/network building activities and local community volunteer programs.

Position Overview:

The position exposes interns to the various components of BRSEP’s functions by involvement in related tasks in drug safety reporting in clinical trials and post-market product use. Interns will contribute to projects, attend departmental team meetings, and work closely with professionals from a multitude of backgrounds, including PhDs, MDs, or PharmDs, in varied specialties, such as Oncology/Hematology, Virology, and Inflammation, or business document experts. The internship is an entry-level position, beginning with an initial period of training under direct supervision.

Key Responsibilities will include, but are not limited to the following:

• Supporting the Therapeutic Area (TA) Teams in the authoring or contributing to sections of signal validation/assessment documents
• Supporting quality control and, where required, authorship of assigned portions of aggregate reports
• Collaborating with Gilead subject matter experts to contribute to the review and creation of risk language for non-Gilead investigational medicinal products
• Participating in both internal and external educational initiatives and activities
• Supporting the TA and BRSEP teams with ad hoc safety projects
• Ensures own work complies with established practices, policies and processes, and any regulatory or other requirement
• Showcase your work with a final presentation (PPT) near the conclusion of your internship

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 Bachelor’s/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