Project Associate, Research
About The Position
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.
Requirements
- High School and Six Years’ Experience OR Associate Degree and Five Years’ Experience OR Bachelor's Degree and Four Years’ Experience OR Masters' Degree and Two Years’ Experience
- Embraces technology, and have advanced working knowledge of Microsoft Word
Nice To Haves
- Bachelor’s degree with regulatory submission experience preferred.
- High school diploma with relevant experience acceptable.
- Attention to detail, patient, organized and thorough.
- Looks for efficiency in processes.
- Self-motivated, willingness to learn and take direction, and has high work ethic.
- Clear and effective communication, able to influence without authority and work in a matrixed environment.
- Operates in a professional, service-oriented manner.
- Resourceful self-starter with problem-solving and critical thinking skills.
- Understands general principles of project management, timelines and interdependencies of deliverables.
- Ability to work collaboratively; experience communicating with stakeholders at all levels is desirable.
- Strong proficiency in Microsoft Office (e.g., Outlook, Word, Excel, PowerPoint, and Teams), Adobe Acrobat, Veeva systems and Smartsheet.
Responsibilities
- Has general understanding of regulatory documents, the electronic common technical document (eCTD) specifications.
- Experience with electronic document management systems, and capable of supporting the lifecycle of regulatory documents, from creation to review and completion.
- Able to format documents in MS Word.
- Understands and adheres to standards and processes, willing and able to do minute and repetitive tasks on the computer.
- Collaborates cross-functionally (Research, Regulatory Affairs, Regulatory Operations, Medical Writing/Content Managers, Clinical Development) to support timely availability of regulatory documents.
- Is able to work in ambiguous situations, sometimes without known precedence, and able to think critically to implement effective solutions.
- Able to manage multiple tasks simultaneously with strong attention to detail and work with tight deadlines, but flexible enough to pivot when necessary.
- Participates in process improvements, new standards, updating systems, and other activities related to continuous improvement in support of submissions.
- Is able to work onsite at least 3 days a week.
Benefits
- company-sponsored medical, dental, vision, and life insurance plans
- discretionary annual bonus
- discretionary stock-based long-term incentives
- paid time off
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
High school or GED
