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Director, Evidence Delivery

3 months ago

Canada, CA TFS HealthScience Full time

Join Our Team as an Evidence Delivery Director

TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and Functional Service (FSP) solutions.

About this role

The Evidence Delivery Director (EDD) will be responsible and accountable for the operational planning, delivery, oversight and budget management of company sponsored studies and/or externally sponsored studies and/or Early Access Programs. The EDD will work hand in hand with the scientific study leader who is responsible for all scientific aspects throughout all stages of the study (epidemiologist for observational studies, Medical Affairs Leader for interventional studies).

As part of our SRS team you will be dedicated to one sponsor, a global patient-focused pharmaceutical company.

Key Responsibilities:
  • Responsible to provide the insights on operational feasibility during the Study Design Concept development process.
  • Drive the process of coordinating protocol development by ensuring input of all relevant cross functional (internal) and external stakeholders.
  • Responsible to provide input on operational feasibility of the protocol.
  • Coordinate all internal, study governance processes (e.g. ERT, MARC, LSPC, ClinicalChallenge).
  • Lead the process for selection of External Service Providers (ESPs), including Clinical Research Organisations (CROs).
  • Set up study team and manage study sourcing.
Qualifications:
  • Bachelor's degree required preferably in medical or biological science or equivalent by experience.
  • Extensive pharmaceutical industry/CRO experience within clinical study/research project delivery, drug development process and relevant guidelines, for example GCP/ICH, for a specific therapeutic and geographical area.
  • Project Management qualification or demonstration of project management skills including scope, budget, timeline, resource management and use of associated tools.
  • Scientific awareness and extensive knowledge of observational study guidelines and SOPs.
  • Extensive knowledge of early and late stage Pharmaceutical Development.
What We Offer

We provide a competitive compensation package, comprehensive benefits, and the opportunity for personal and professional growth in a rewarding environment. You'll be joining a team that values collaboration, innovation, and making a difference in the lives of patients.

A Bit More About Us

Our journey began over 27 years ago in Sweden, in the city of Lund. As a full-service, global Contract Research Organization (CRO), we build solution-driven teams working towards a healthier future. Bringing together over 800 professionals, TFS delivers tailored clinical research services in more than 40 countries with flexible clinical development and strategic resourcing solutions across key therapeutic areas including Dermatology, Neuroscience, Oncology, and Ophthalmology.

Our core values of Trust, Quality, Passion, Flexibility, and Sustainability are our guiding light serving as the framework for decision-making at all levels of the organization. They assist us in attracting and retaining valuable talent who share our sentiments, resulting in high employee engagement and satisfaction. By aligning on these fundamental values, we cultivate a unified force, geared towards innovation and excellence. This collective effort propels us towards our shared goal and fosters a culture of mutual respect and collaboration. Together we make a difference.

Department: SRS North America
Locations: Canada
Remote status: Hybrid
Employment type: Full-time
REQ ID: 216988
Work Arrangement: Hybrid

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