
Project Associate, Research
United States - California - Foster CityResearchRegularJob Description
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
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.
Embraces technology, and have advanced working knowledge of Microsoft Word
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.
Basic Qualifications:
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
Preferred Qualifications:
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.
People Leader Accountabilities
Create Inclusion - knowing the business value of diverse teams, modeling inclusion, and embedding the value of diversity in the way they manage their teams.
Develop Talent - understand the skills, experience, aspirations, and potential of their employees and coach them on current performance and future potential. They ensure employees are receiving the feedback and insight needed to grow, develop, and realize their purpose.
Empower Teams - connect the team to the organization by aligning goals, purpose, and organizational objectives and holding them to account. They provide the support needed to remove barriers and connect their team to the broader ecosystem.
For additional benefits information, visit:
https://www.gilead.com/careers/compensation-benefits-and-wellbeing
* Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.
For jobs in the United States:
Gilead Sciences Inc. is committed to providing equal employment opportunities to all employees and applicants for employment, and is dedicated to fostering an inclusive work environment comprised of diverse perspectives, backgrounds, and experiences. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, sex, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job related characteristics or other prohibited grounds specified in applicable federal, state and local laws. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact ApplicantAccommodations@gilead.com for assistance.
For more information about equal employment opportunity protections, please view the 'Know Your Rights' poster.
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For Current Gilead Employees and Contractors:
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