Global Feasibility Director

PUB368938

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

Requirements

Requirements

▪ 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

Benefits

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Any questions remaining?

Your consultant, Quynh Vo is happy to clarify anything about this vacancy. When reaching out, use the pub number:
PUB368938

Account manager

Quynh Vo
Brunel Canada - Calgary
q.vo@brunel.net

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