Graduate Intern - Medical Safety Science, Patient Safety, Virology

Gilead Sciences

Nov 6, 2023

Applications are closed

Internship
Full-time
Off-cycle Internship
Science
San Francisco

Requirements

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/PharmD program at an accredited US based university or college
Must be a Rising Sophomore, Junior, or Senior as 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
Have a basic understanding of the role of drug safety within the pharmaceutical industry
Demonstrated ability to be a fast learner.
Demonstrated ability to be flexible and adaptable to change
Strong interpersonal skills and understanding of team dynamics.
Proven ability to work successfully in a team-oriented, highly-matrixed environment.
Demonstrates good analytical thinking skills, attention-to-detail, good communication and writing skills, project management skills and proficiencies with Microsoft Office suite.
If needed, ability to travel.

Responsibilities

Supports authoring or otherwise contributes to the preparation of aggregate safety reports and risk management plans (RMPs).
Conducts signal detection and evaluation activities for assigned products in collaboration with the Global TA Safety Physician and Scientist as part of the continuous benefit-risk evaluation throughout the product lifecycle.
Supports implementation of decisions from the signal evaluation process, including updates to core safety information, Investigator’s Brochure and other key safety documents and deliverables.
May contribute to Patient Safety activities and input related to regulatory filings, New Drug Applications [NDAs], Biologics License Applications [BLAs]), and responses to safety queries from third parties, such as regulatory agencies.
May perform safety reviews of clinical trial protocols, Investigator’s Brochures, clinical study reports, informed consent forms, and other study related documents.
Ensures own work complies with established practices, policies, and processes, and any regulatory or other requirements.
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?”