Evidence Delivery Associate Director - Barcelona, España - TFS HealthScience

TFS HealthScience
TFS HealthScience
Empresa verificada
Barcelona, España

hace 1 mes

Isabel García

Publicado por:

Isabel García

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Descripción

TFS HealthScience is excited to be expanding our
SRS team and we are looking for an experienced, highly motivated
Evidence Delivery Associate 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 cores 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 organisation.


Together we make a difference.
TFS HealthScience is looking for an
Evidence Delivery Associate 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 homebased employees
  • Lunch Allowance
  • Flexible working schedule

Responsibilities

  • Company Sponsored Observational and Interventional Research:
  • Support/coordinate protocol development and finalization
  • Manage Study Governance (post SDC)
  • Support/coordinate all internal, study governance processes (e.g. MEORT, MARC, LSPC, Clinical Challenge)
  • External Service Provider Management
  • Provide input into the selection of External Service Providers (ESPs), including Clinical Research Organisations (CROs)
  • Support strategic handover meetings and kick off meetings
  • Perform CRO oversight to help ensure project delivery within time, cost and quality
  • Collaborate with CRO/ESP to ensure the study operational aspects are effectively undertaken and that they have clear remits for delivery
  • Manage study specific issues and escalations with ESPs/CROs
  • Stakeholder Management
  • Support Project team setup and study sourcing activities
  • Support effective collaboration with the scientific/medical counterpart, the Epidemiologist/Medical Affairs Leader (MAL) respectively, as well as other internal cross functional global roles
  • Report study updates for areas of responsibility from a time, cost and quality perspective to internal stakeholders (e.g. Evidence Delivery Associate Director(EDAD)
  • Support implementation and upkeep of an effective communication approach, as well as roles and responsibilities between the BPM Evidence stakeholders, local AZ and External Service Providers
  • Coordinate efforts/input of the external scientific community (e.g. (International Coordinating Investigators, Steering/Executive Committee) during project design and delivery
  • If leading a study, develop and maintain the overall study budget (internal and external study costs)
  • Ensure transparency over areas of budget responsibility by updating through relevant systems (s.a. ACCORD) and platforms (PPC meetings) and obtaining approval for budget changes
  • Work with procurement on project agreement and manage subsequent out of scope changes for ESP/CRO
  • Manage and reconcile Contracts, POs and invoices
  • Support financial audit readiness and Sox attestation as needed
  • Support delivery of projects to agreed timelines (scorecard), within the approved budget and according to client quality standards
  • Support global oversight over the operational study start up, implementation and closure and ensure inspectionreadiness
  • Support implementation of studyrelated change management within business strategy, s.a. assessment of scope changes
  • Ensure Compliance with client Procedural Documents, Standards and Policies, international guidelines and local regulations at any time, and report compliance breaches
  • Undertake feasibility assessments with internal and external stakeholders
  • Manage study systems reporting
  • Supports the review of ESR proposals and protocols to enable a consistent, high quality approach to evaluation
  • Manage across a range of global and local crossfunctional stakeholders to ensure all client obligations and responsibilities for ESR (e.g. drug supply, contracting, regulatory documentation, publication review etc.) are met
  • Manage external stakeholder, e.g. external Investigator and Sponsoring institutions
  • Support ESR portfolio financial forecasting and budgeting for assigned ESR studies/portfolios, utilising appropriat
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