Precision For Medicine

Senior Project Manager – Clinical Trials

Precision For Medicine

full-time

Posted on:

Location Type: Remote

Location: Spain

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Job Level

About the role

  • 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
  • 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 reviews 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 4 years full service Project Management experience in a clinical trial setting working for a Clinical Research Organisation.
  • Experience managing studies within Oncology
  • 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.
Benefits
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Applicant Tracking System Keywords

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Hard Skills & Tools
project managementclinical trial managementdata managementbiostatisticsmedical monitoringprotocol preparationperformance metricsOncology experienceGCP guidelinesICH guidelines
Soft Skills
interpersonal skillsorganizational skillscustomer servicecommunication skillspresentation skillsrelationship buildingteam collaborationleadershipproblem-solvingobjective setting
Certifications
degree in life sciencesclinical research certification