Global Feasibility Lead

PUB308305

About this role

About this role

We’re inviting candidates for a Global Feasibility Leader, for a Global and innovative pharmaceutical company head-quartered in Canada. This is a 1-year contract position, requiring on-site presence a few days a week once Covid-19 restrictions allow.

Champion the best use of data to drive strategic and operational feasibility, including site identification, and recommendations to improve our patient recruitment/retention strategies. This role will span from early to late stage medicines development across all TAs and from the concept stage through to execution.

Working across the functions of Development Operations, TA leads and CROs, the Feasibility and Recruitment Partner will enable expedited, predictive delivery for all stages of global feasibility. This ensures standardization in how we use data, tools and process to inform quality decision making at TA, indication, program and study levels.

Responsibilities

  • Working closely with study design teams enabling data-driven approaches to support balanced and informed decisions, and improve predictability of execution
  • Using data assets, advanced analytical models, and interpret data to provide recommendations to study teams to support planning and execution
  • Linking with internal groups for patients and site insights, ensuring a truly patient centric approach in your work
  • Become the expert user for the new study design and planning digital platform and optimization models, providing continuous improvements of tool features to meet current practice needs
  • Leading standardized design feasibility offering, using data intelligence (historical and RealWorld Data RWD), and insights from key external and internal specialists to support study teams from program concept to protocol design and study set-up

In this role you will be the authority on planning and delivering robust strategies for feasibility across a broad portfolio including end-to-end operational feasibility. This will help to inform site selection and baseline recruitment forecasts and study landmarks.

Requirements

Requirements

Requirements

  • Bachelors degree in relevant field (e.g. life sciences, business management, project management)
  • Significant experience within Drug Development and Feasibility in a pharmaceutical setting
  • Validated capabilities in data analysis, data interpretation to drive inform decision making
  • Experience developing study delivery strategies and tactical/operational plans aligned to commercial and regulatory objectives
  • Clinical trial patient and investigator recruitment and retention experience
  • Project and budget management, within a Global environment

Benefits

Benefits

Why apply through Brunel? Finding the next step in your career can be a fulltime job in itself. We manage the process for you: from submitting your resume to coordinating interviews to extending offers and assisting with on-boarding. We’ll get you going while you get on with the job.

Join the Brunel Family

Join the Brunel Family

Brunel has a reputation for working with some of the best in the business. That’s what we continually strive for. Over 45 years, we’ve created a global network of interesting clients and talented individuals working together through a vast array of services.

Start applying immediately

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, Paula Domingues Clarkson is happy to clarify anything about this vacancy. When reaching out, use the pub number:
PUB308305

Account manager

Paula Domingues Clarkson
Brunel Brazil - Rio de Janeiro
p.clarkson@brunel.net

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