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Graduate Intern - Real World Evidence
Company | Gilead Sciences |
Address | Foster City, CA, United States |
Employment type | FULL_TIME |
Salary | |
Category | Biotechnology Research,Pharmaceutical Manufacturing |
Expires | 2023-10-13 |
Posted at | 8 months ago |
For Current Gilead Employees And Contractors
- Work with his/her supervisor to decide on a epidemiology research project, based on the experience and interest of the intern (within the scope of Real World Evidence (RWE) post authorization studies (PAS), pharmacoepidemiology, or established products regarding safety and effectiveness)
- With guidance and direction from the supervisor, learn to develop a study protocol and/ or statistical analysis plan to describe the research design and method
- At the conclusion of the internship, the intern will give a presentation summarizing the research project completed during the program
- Learning how to address the challenges with the project or data through presentation of scientific evidence
- Conduct analysis using in-house real-world database (e.g., insurance claims, electronic medical records, or from an existing post-marketing Phase IV study)
- Learn different research methodologies used in conducting real-world studies
- Attending and participating in group discussions within RWE and across other departments.
- Learn the ability to handle multiple tasks, maintain clear tracking and documentation, and manage tight project timelines
- Develop knowledge of other roles and functions within Real-World Evidence and cross-functional team.
- Must be enrolled full-time in the Fall Semester at an accredited university/college after the completion of the internship
- Must be currently enrolled as a full-time student in a Masters or PhD program at an accredited US based university or college pursuing a degree in Epidemiology, Public Health, or a related field
- Self-motivated, adaptable to a dynamic environment
- Strong organizational, time-management, interpersonal and communication capabilities
- Must have a minimum GPA of 2.8
- Must have a good working knowledge of SAS, STATA, SQL, or R
- Must be able to complete a 10-12 consecutive week internship between May and August
- Ability to work both independently and collaboratively
- Must be able to relocate if necessary and work at the designated site for the duration of the internship
- Must be at least 18 years old
- Authorized to work in the United States without Sponsorship now or in the future or CPT/OPT through your University
- Excellent detail oriented analytical, problem-solving skills
- Efficient, organized, and able to handle short timelines in a fast-paced environment
- Demonstrated commitment to inclusion and diversity in the workplace
- Demonstrated experience with observational research
- Proficiency with MS Office Suite
- Ability to work both independently and collaboratively
- Experience with secondary data analysis, including electronic medical record and/or medical claims databases
- Ability to identify issues and seek solutions
- Integrity (Doing What’s Right)
- Accountability (Taking Personal Responsibility)
- Excellence (Being Your Best)
- Teamwork (Working Together)
- Inclusion (Encouraging Diversity)
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