Pnd-662 Evidence Delivery Director

Detalles de la oferta

.TFS HealthScience is excited to be expanding our SRS team and we are looking for an experienced, highly motivated Evidence Delivery Director who shares our vision of providing clinical research excellence. Our SRS team is a highly experienced international group of professionals led by an industry expert. We are a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. We combine the full-service capabilities and global reach of a large CRO with the flexibility and personal approach only a mid-size CRO can deliver. Our core values of Trust, Quality, Flexibility, Passion, and Sustainability are what makes TFS HealthScience the successful company it is today. Our values shape our culture and work ethic. They reflect what we stand for and guide our organization. Together we make a difference. TFS HealthScience is looking for an Evidence Delivery Director in Barcelona. What can we offer you? A great place to work where you will get the chance to push your career to the next level, a global environment with global opportunities. You will also get the opportunity to be part of a team with highly intelligent, passionate experts from all over the world. TFS is a place for inspiration where we focus on the patients, saving lives and aiming to increase their quality of life by supporting our clients. Spain benefits include: Private Health Coverage Global General Liability Insurance Global Travel Insurance Homebased Allowance for home-based employees Lunch Allowance Flexible working schedule Responsibilities Cross-functional collaboration and stakeholder management to drive operationally viable outcomes Operational delivery input on feasibility of a proposed study or project Contribute to Governance reviews of global studies (also including local studies upon agreement EDGD) and other relevant forums as required (e.G. GPT, JPT, etc.) Support the development of one-pagers in close collaboration with Payer & Strategy Leads Process improvements, e.G. RFP process, ballparking, feasibility, etc. Mentoring, sharing of lessons learned, best practices, problem solving Early engagement with CRO partners and RFP process Responsible to provide insights on operational feasibility during the SDC 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 Core member of ERT and other planning/life cycle meetings, representing Evidence Delivery to provide operational expertise into Study Design Concepts and Study Protocols Plan & ensure adherence to all internal, study governance processes (e.G


Salario Nominal: A convenir

Fuente: Jobtome_Ppc

Requisitos

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