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Senior Clinical Project Manager

hace 2 meses


Madrid, Madrid, España Precision Medicine Group A tiempo completo
About the Role

We are seeking a highly experienced Senior Clinical Project Manager to join our global team at Precision Medicine Group. As a Senior Clinical Project Manager, you will be responsible for leading clinical projects in accordance with the study budget and scope of work.

Key Responsibilities
  • Independently lead clinical projects in accordance with the study budget and scope of work.
  • Use strong interpersonal and organizational skills to set and achieve objectives in the execution of the projects; both contracted objectives and financial objectives.
  • May be called upon to run international trials as well.
  • Serve as the primary point-of-contact liaison with the client to provide excellent customer service, including participation in proposal activities and client presentations.
  • Liaise with Project Team and senior management of both Precision and sponsors, including C-level.
  • Handle and lead all aspects of a clinical research trial or trials.
  • Total project management for all functional areas including data management, safety, clinical, medical monitoring and biostatistics, etc.
  • Prepare project status updates for clients and management; identifying key deliverables and performance metrics of success and escalation.
  • Serve as an active member of the Project Team with the goal to contribute towards efficient management and execution of trials.
  • Prepare and review protocols and other study documentation such as project plans, inform consents, site contracts and budgets.
Requirements
  • Degree or similar related life science qualification, or equivalent combination of education and experience.
  • Previous experience in a full service/global Project Management role working in the CRO industry is essential.
  • 5 to 7 years industry experience and at least 3 years full service Project Management experience in a clinical trial setting working for a Clinical Research Organisation.
  • Working understanding of GCP/ICH guidelines and the clinical development process.
  • Ability to drive and availability for domestic and international travel including overnight stays.
  • Be able to communicate effectively in the English language both written and spoken.
  • Strong presentation skills.
  • Proven computer skills (MS Office, MS Project, PowerPoint) and software experience (CTMS, eTMF, EDC, IXRS).
  • Proven ability to develop positive working relationships with individual and teams internally and externally.
  • Demonstrated core understanding of medical terminology and clinical trial activities as it relates to the execution of a clinical development plan.