Early Talent Program Associate - PDR

Chez Roche, vous pouvez être vous-même et être apprécié pour les qualités uniques que vous apportez. Notre culture encourage l'expression personnelle, le dialogue ouvert et les connexions authentiques, où vous êtes valorisé, accepté et respecté pour ce que vous êtes, vous permettant de prospérer tant personnellement que professionnellement. Voici comment nous visons à prévenir, arrêter et guérir les maladies et à garantir à chacun l'accès aux soins de santé aujourd'hui et pour les générations à venir.

Rejoignez Roche, où chaque voix compte.

La 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.

The opportunity:

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.

Who you are:

You hold a minimum qualification of a first degree in a life sciences, biological sciences, biology, chemistry, Pharmacy, or related field before the start of the program from which you have graduated from within the past 2 years. And you are within two years of completion of a degree program in the before mentioned disciplines.

You have 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.

Additional Information:

Division:
Pharma

Department:
Global Product Development Regulatory (PDR)

Reports to:

Functional/Senior Functional Manager

Location:

Hybrid, Based in Mississauga, ON

Hours:

full-time (35 hours per week)

Length:
This opportunity is a 2-year work term.

Appro…