Senior Trial Vendor Lead – Clinical Operations (Hybrid)

ES06 (FCRS = ES006) Novartis Farmacéutica, S.A.

Sabadell

Hybride

EUR 46 000 - 86 000

Plein temps

Il y a 9 jours

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Avantages offerts par ce poste

Hybrid working options
Insurance plans
Retirement plans
Wellbeing resources
Global recognition programs
14 weeks parental leave

Résumé du poste

Novartis Farmacéutica, S.A. is seeking a Trial Vendor Manager to lead the Clinical Trial Team’s vendor sub-workstream, overseeing vendor service delivery, study timelines, budgets, quality, and compliance.

The role partners with the Vendor Start-up Manager across labs, IRT, eCOA/ePRO, imaging and PR&R to ensure timely study initiation. You will manage vendor-related risks, translate protocols into vendor specifications, supervise UAT for eCOA/IRT, and drive site activation from a vendor

Qualifications

  • Bachelor’s degree in Life Sciences or equivalent.
  • Minimum of 3 years’ clinical operations experience, including direct operational management and oversight of clinical trial vendors.
  • Strong knowledge of GxP and ICH regulations, clinical trial design, and supplier service specifications.
  • Proficiency in vendor management, contracting, and site-related collaborations, including UAT for eCOA and IRT systems.
  • Results-driven with proven ability to complete projects within timelines.
  • Excellent interpersonal, negotiation, problem-solving, and communication skills in a matrixed environment.

Responsabilités

  • Act as the single point of contact for vendor service delivery at the study level, partnering with vendors and cross-functional teams.
  • Provide direct, end-to-end operational oversight of vendor deliverables, ensuring alignment with timelines, scope, quality, and compliance expectations across major vendor categories.
  • Review vendor-related protocol sections during protocol development and translate requirements into accurate vendor specifications and Statements of Work (SOWs).
  • Oversee vendor financials, including forecasting, budget tracking, validation of work performed, service confirmations, invoice reconciliation, and purchase order management and close-out.
  • In collaboration with vendors, study start up leads and vendor start up managers, ensure that all key vendor deliverables and documentation are in place to support submission during study start-up.
  • Lead UAT activities for vendor systems (e.g., eCOA, IRT), and contribute to vendor system validation.
  • Drive site activation from a vendor perspective, compile vendor related central documents, and address risks/issues during site activation and throughout the life-cycle of a site.
  • Manage vendor performance against agreed KPIs, proactively identify risks and issues, drive corrective actions and mitigation plans with vendors and study teams, and maintain complete, inspection-ready oversight documentation.

Connaissances

Vendor management
Clinical trials
GxP knowledge
Communication skills
Negotiation
Project planning

Formation

Bachelor’s degree in Life Sciences or equivalent
Advanced degree preferred

Outils

eCOA/IRT systems

Description du poste

Novartis Farmacéutica, S.A. is seeking a Trial Vendor Manager to lead the Clinical Trial Team’s vendor sub-workstream, overseeing vendor service delivery, study timelines, budgets, quality, and compliance.

The role partners with the Vendor Start-up Manager across labs, IRT, eCOA/ePRO, imaging and PR&R to ensure timely study initiation. You will manage vendor-related risks, translate protocols into vendor specifications, supervise UAT for eCOA/IRT, and drive site activation from a vendor

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