Global Feasibility Director


About this job

  • Market: Life Sciences & Health Care
  • Branch: Pharmaceutical
  • Area of Expertise: Research & Development
  • Location: MISSISSAUGA

What is required?

  • hours per week: 40
  • Education level: Professional Bachelor
  • Closing date: Saturday, 22 October 2022

About this role: Global Feasibility Director

We are currently hiring a Global Feasibility Director for our client, a global pharmaceuticalcompany known for its innovative technology and products in nutrition, diagnostics, medicaldevices, and branded generic pharmaceuticals.

The Global Feasibility Director will play a critical role by providing data-driven strategic design andoperational feasibility. This is a permanent role with a hybrid working model and an opportunity topartner with important stakeholders internally as well as externally

Responsibilities▪ Proactively lead standardized design feasibility offering, by using data intelligence andinsights from key external and internal authorities to support study teams fromprogram concept to protocol design and study set-up
▪ Partner with study design teams to enable data-driven approaches, and informeddecision making and improve the predictability of execution▪ Use relevant internal and external data assets, sophisticated analytical models, andinterprets data to provide recommendations to study teams in a significant way tosupport planning
▪ Secure traceability of assumptions and visibility in decisions for end-to-end process



▪ Bachelor’s degree in life sciences, business management, project management, orrelevant field, master’s degree is desirable▪ Experience with Drug Development and Feasibility in the pharmaceutical industry▪ Experience working with partners, CROs/AROs▪ Validated experience in the development of business the cases▪ Demonstrated experience in data analysis, and data interpretation to drive informeddecision making▪ Hands-on experience in building, managing, and influencing relationships andachieving results with senior partners in conflicting priority environment▪ Experience in developing study delivery strategies and tactical/operational plansaligned to commercial and regulatory objectives▪ Experience in relevant core therapeutic areas/indication▪ Clinical trial patient and investigator recruitment and retention experience▪ Validated experience in project and budget management▪ Experience working with Global teams is an asset▪ Experience with new product development in the pharmaceutical industry is an asset▪ Proven project/program management or other complex /cross-border managementexperience is desired


What We OfferWhy apply through Brunel? Finding the next step in your career can be a full-time job in itself. Wemanage the process for you: from submitting your resume to coordinating interviews to extendingoffers and assisting with onboarding. We will get you going while you get on with the job

Join the Brunel Community

Join the Brunel Community

About UsBrunel has a reputation for working with some of the best in the business. That is what we continuallystrive for. Over 45 years, we have created a global network of interesting clients and talentedindividuals working together through a vast array of services.

Start applying immediately

Sending an application is quick and easy. Just make sure you have the required documents ready to go.

  • Certifications (optional)
  • Job references (optional)
  • Motivation Letter (optional)
  • Resume
Apply now

Any questions remaining?

Your consultant, Quynh Vo is happy to clarify anything about this vacancy. When reaching out, use the pub number:

Account manager

Quynh Vo
Brunel Canada - Calgary

Other people also looked at