Genentech Pharmaceuticals Regulatory Policy Fellowship
OVERVIEW:
Regulatory Policy Fellows are assigned their responsibilities as business needs dictate, and often perform work that transcends multiple or all therapeutic areas. Regulatory Policy Program Fellows work in close coordination with other members of the policy team and under the supervision of their manager. They project manage the implementation of regulatory policy strategies based on regulatory and legislative trends important to Roche's product portfolio. Regulatory Policy Fellows support and participate in activities with trade associations, think tanks, advocacy organizations, and regulatory authorities. They are also responsible for identifying, documenting, coordinating, and communicating regulatory policy activities and information.
WHO ARE WE:
Genentech is a biotechnology company dedicated to pursuing groundbreaking science to discover and develop medicines for people with serious and life-threatening diseases. Regulatory Policy is part of the broader Product Development Regulatory (PDR) organization that interprets the needs of worldwide health authorities and provides strategic information necessary to advance the development and business priorities of the Roche Group. PDR policy is committed to developing regulatory frameworks that are evidence-based, innovative, ethical, and influential in the industry.
JOB SUMMARY:
The fellow will function as a Regulatory Policy Analyst and will support the Regulatory Policy team on the following activities at Genentech:
- Continues to expand his/her knowledge base of laws, regulations, and guidelines governing the development, licensure, and marketing of drugs and biologics.
- Obtains and applies in-depth knowledge of regulatory guidelines, procedures and best practices.
- Writes, coordinates analyze, and/or reviews comments on regulatory or legislative initiatives and guidance.
- Supports interactions on policy and advocacy issues, including building relationships with key regulatory decision makers.
APPLICATION REQUIREMENTS:
- Curriculum Vitae
- Letter of Intent
- Official Transcript
- 3 Letters of Recommendation
ELIGIBILITY CRITERIA:
Graduated with PharmD or Ph.D.