About this role
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.
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).
In addition, the EDD will support BPM Evidence's continuous improvement by developing expertise in a specific area of study delivery, serving as a point of contact for best practices, and contributing to the development and maintenance of guidance documents and training materials. Usually, the EDD's focus will be on one of the three main types of work as described below:
Key ResponsibilitiesCompany Sponsored Observational and Interventional Research:Early input into evidence generation planningContribute to continuous development of Evidence DeliveryInput into Study Design Concept (SDC)Accountable for protocolManage Study Governance (post SDC)External Service Provider ManagementStakeholder ManagementManage study financeOther Project Management activitiesExternally Sponsored Scientific Research (ESR):Governance - DeliveryEarly Access (EA) / Named Patient Supplies (NPS)RequirementsBachelor'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.Ability to effectively work with Clinical Research Organisations/External Providers.Proven ability to interact widely and effectively within the company across regions, functions, and cultures.Experience and knowledge within compliant management of Externally Sponsored Scientific Research.Persuasive communicator in English with a proven ability to work collaboratively in a multi-cultural environment.Open to periods of travel.TFS HealthScience collects and processes personal data in accordance with applicable data protection laws. If you are a European Job Applicant, see the privacy notice for further details.
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