Early Talent Associate - PDR

Roche • Mississauga, ON

1d • CA$71,544 - CA$93,902 • Hybrid

About The Position

Embark on a transformative two-year journey with the One PDR ET Program, meticulously crafted to impart comprehensive foundational knowledge in regulatory affairs. This dynamic initiative blends hands-on assignments with tailored learning solutions, making it an ideal entry-point for aspiring regulatory professionals. Eligible candidates should possess a Bsc in life or pharmaceutical sciences, or an equivalent scientific qualification, and have less than one year of relevant pharmaceutical regulatory experience. Participants gain invaluable insights into the complete lifecycle of pharmaceutical products, from initial clinical trials to market exit, by engaging in diverse activities across various therapeutic areas and stages of development. The latter part of the program offers the opportunity to rotate into another Product Development function or specialize further in PDR. Throughout the program, ETs collaborate with global drug development teams to support the introduction of novel pharmaceutical products to patients worldwide. This environment not only enhances their scientific writing skills but also deepens their understanding of regulatory frameworks by preparing a wide array of regulatory documents. By joining the One PDR ET Program, participants become pivotal contributors to the regulatory landscape, dedicated to ensuring that life-changing medicines reach those who need them most.

Requirements

• Minimum qualification of a first degree in a life sciences, biological sciences, biology, chemistry, Pharmacy, or related field before the start of the program.
• Within two years of completion of a degree program in the before mentioned disciplines.
• Basic understanding of drug development and entry level understanding of the role of a regulatory professional.
• Maximum 1 year relevant pharmaceutical experience post last degree.
• Demonstrates a learning mentality, engages in personal growth, and actively seeks and acts on feedback.
• Fosters partnership, collaboration, empowerment, and autonomy to build a strong community.

Responsibilities

• Delivers on projects with mentorship and actively builds foundational regulatory experience with the support of colleagues.
• Owns their learning and development, actively seeking to understand drug development and regulatory roles, and engaging in knowledge sharing and peer support.
• Responsible for understanding and applying business processes to deliver foundational regulatory deliverables.
• Engages with the team through active listening, practicing open communication, and building trust within regulatory and cross-functional teams.
• Grasps the vision of the Roche organization, understanding how their work impacts the team and contributes to overall goals.
• Improves prioritization and time management skills while spending significant time on-site at Roche/Genentech offices.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level