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Global Clinical Project Manager

Global Clinical Project Manager

Pharmaceutical Research Associates, Incmadrid, España
Hace 21 días
Descripción del trabajo

As a Global Clinical Project Manager, you will join the world's largest & most comprehensive clinical research organization, powered by healthcare intelligence. This is a permanent, full-time role through ICON on FSP, dedicated to a global pharma, and fully home-based.

You must currently be working as a Global Clinical Project Manager within a CRO or Pharma setting, with strong vendor management experience.

Responsibilities

What you will be doing :

  • Lead the Study Management Team, providing updates on deliverable status.
  • Ensure availability of reports to support real-time trial status tracking.
  • Manage documentation and communication of trial progress.
  • Maintain inspection-readiness of the Study Management Team.
  • Act as primary contact for Country and Regional staff.
  • Partner with the Global Trial Lead from planning to close-out.
  • Ensure issue escalation and resolution.
  • Work with Trial Team to resolve CAPAs; serve as CAPA owner or contributor.
  • Support site selection through data collection.
  • Participate in feasibility assessments.
  • Establish and monitor enrollment commitments and contingency plans.
  • Track and file trial data timely and accurately.
  • Perform Annual Quality Review of files.
  • Ensure proper archiving and retention of documents.
  • Manage country budgets and monitor expenses.
  • Oversee vendors and review invoices.
  • Create and update trial-specific documents.
  • Contribute to cross-functional documents and submissions.
  • Develop training materials and deliver training as needed.
  • Build strong relationships with internal stakeholders.
  • Ensure protocol compliance and participate in inspections and audits.
  • Support therapeutic knowledge and process improvements.
  • Lead or participate in special initiatives.

Qualifications

You are :

  • BS degree or equivalent in Life Sciences, with 6+ years of clinical trial management experience.
  • Therapeutic area experience.
  • Strong knowledge of ICH-GCP, laws, and regulations.
  • Proven track record managing trials from start-up to closure.
  • Effective leadership and stakeholder management skills.
  • Experience leading virtual, global or regional teams.
  • Strong project management skills and proactive risk mitigation.
  • Proficient in Microsoft Office, TMF, CTMS, and willing to learn new systems.
  • Monitoring or relevant experience preferred.
  • Fluent in local language and English.
  • Excellent communication, analytical, and presentation skills.
  • Understanding of country-specific budget and cost drivers.
  • What ICON can offer you : We prioritize building a diverse culture that rewards high performance and nurtures talent. Benefits include :

  • Annual leave entitlements.
  • Health insurance options.
  • Global Employee Assistance Programme.
  • Life assurance.
  • Flexible benefits such as childcare vouchers, gym memberships, and more.
  • Visit our careers site to learn more about working at ICON. We value diversity, inclusion, and belonging, and are committed to providing an accessible environment for all candidates. We encourage you to apply regardless of whether you meet all requirements—your qualities may be exactly what we need.

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