Clinical Project Manager

hace 2 semanas


Barcelona, Barcelona, España Tfs Healthscience A tiempo completo

About Tfs Healthscience

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Tfs Healthscience is a leading global 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.

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About the Role

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We are seeking an experienced Clinical Trial Manager/Project Manager to manage projects in accordance with company policies, SOPs, regulatory requirements, financial, and contractual obligations.

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As part of our SRS/FSP team, you will be dedicated to one sponsor, a global biotech specialized in Oncology. Your key responsibilities will include:

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  • Ensuring projects are delivered on-time, within scope, and within budget and in compliance with applicable quality standards;">
  • Managing the strategic aspects of projects, identifying, analyzing, and minimizing/mitigating any risk, including the implications of different technical and operational choices;">
  • Communicating effectively with clients to successfully manage the relationship, identify needs, and evaluate alternative business solutions and strategies;">
  • Developing and maintaining project plans and timelines for their project and tracking progress;">
  • Ensuring all study team members are adequately trained on project-specific systems and procedures;">
  • Implementing and maintaining sound business practices;">
  • Measuring and evaluating project performance;">
  • Managing the project budget, profitability, and ensuring invoicing is performed on time and in accordance with the scope of work;">
  • Working with the Finance Accounting team to analyze profitability, revenue, margins, and utilization across their projects;">
  • Managing resource allocation on the project, in collaboration with respective line managers;">
  • Facilitating internal and external communication;">
  • Reporting and escalating to management as needed;">
  • Establishing and maintaining relationships with third parties/vendors;">
  • Managing high-level deliverables across the organization;">
  • Participating in capability presentations/bid defenses, as needed;">
  • Continually defining ways to increase customer satisfaction and deepen client relationships;">
  • Contributing in review/developing procedures, guidelines, SOPs, metrics as needed;">
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Requirements

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To be successful in this role, you will need:

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  • ">
  • Over 5 years of experience, preferably in early-stage oncology development, and within small, dynamic biotechnology companies;">
  • Hands-on experience as a Clinical Research Associate (CRA) combined with study management experience;">
  • A strong background in clinical trial management, including vendor selection, study initiation, execution, monitoring, and closure of clinical studies;">
  • Proven experience in contingency planning and risk management during clinical trials;">
  • A preference for candidates with experience working in small, fast-paced biotech companies;">
  • Native Spanish speaker is required, with a good command of English;">
">

Estimated Salary: €60,000 - €80,000 per annum


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