Clinical Project Manager

hace 5 días

Barcelona, España Tfs Healthscience A tiempo completo

.Clinical Trial Manager - Home based in Spain or Hybrid based in BarcelonaAbout this roleTFS HealthScience is a leading global, mid-size 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.The Clinical Trial Manager / Project Manager has the overall responsibility for managing projects in accordance with company policies, SOPs, regulatory requirements in addition to financial and contractual obligations.As part of our SRS/FSP team, you will be dedicated to one sponsor, a global biotech specialized in Oncology.ResponsibilitiesEnsure that projects are delivered on-time, within scope and within budget and in compliance with applicable quality standards.Manage the strategic aspects of projects, identify, analyze and minimize/mitigate any risk, including the implications of different technical and operational choices.Communicate effectively with clients to successfully manage the relationship, identify needs and evaluate alternative business solutions and strategies.Develop and maintain Project Plans and timelines for their project and track progress.Ensure all study team members are adequately trained on project specific systems and procedures.Implement and maintain sound business practices.Measure and evaluate project performance.Manage the project budget, profitability and ensure invoicing is performed on time and in accordance with the scope of work.Work with the Finance Accounting team to analyze profitability, revenue, margins and utilization across their projects.Manage the resource allocation on the project, in collaboration with respective line managers.Facilitate internal and external communication.Report and escalate to management as needed.Establish and maintain relationships with third parties/vendors.Manage high-level deliverables across the organization.Participate in capability presentations/bid defenses, as needed.Continually define ways to increase customer satisfaction and deepen client relationships.Contribute in review/develop procedures, guidelines, SOPs, metrics as needed.RequirementsMinimum Experience: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.Technical Knowledge:Strong background in clinical trial management, including vendor selection, study initiation, execution, monitoring, and closure of clinical studies.Risk Management:Proven experience in contingency planning and risk management during clinical trials.Biotechnology Environment:Preference for candidates with experience working in small, fast-paced biotech companies.Language:Native Spanish speaker is required, with a good command of English

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