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Precision for Medicine

Global CRO for precision medicine trials

Senior Clinical Project Manager - Oncology

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeRemote in SpainNo salary listed

About the Job

Requirements

  • A degree or similar related life science qualification, or an equivalent combination of education and experience.
  • Previous experience in a full-service or global project management role in the CRO industry is essential.
  • Extensive experience working in a Clinical Operations position within a CRO, with at least 4 years of full-service project management experience in a clinical trial setting at a Clinical Research Organisation.
  • Experience managing studies within Oncology.
  • Working understanding of Good Clinical Practice (GCP) and International Council for Harmonisation (ICH) guidelines and the clinical development process.
  • Ability to drive and availability for domestic and international travel, including overnight stays.
  • Ability to communicate effectively in English, both written and spoken.
  • Strong presentation skills.
  • Proven computer skills in Microsoft Office, Microsoft Project, and PowerPoint, and software experience with CTMS, eTMF, EDC, and IXRS.
  • Proven ability to develop positive working relationships with individuals and teams internally and externally.
  • Core understanding of medical terminology and clinical trial activities as they relate to executing a clinical development plan.

Responsibilities

  • Independently lead clinical projects in accordance with the study budget and scope of work, setting and achieving contracted and financial objectives during project execution; may lead international trials.
  • Serve as the primary client point of contact and liaison, providing customer service and participating in proposal activities and client presentations.
  • Liaise with project teams and senior management at Precision and sponsor organizations, including C-level stakeholders.
  • Handle and lead all aspects of one or more clinical research trials.
  • Manage all functional areas of projects, including data management, safety, clinical, medical monitoring, and biostatistics.
  • Prepare project status updates for clients and management, identifying key deliverables, success metrics, and escalation needs.
  • Actively participate in the project team to contribute to efficient trial management and execution.
  • Prepare and review protocols and other study documentation, including project plans, informed consents, site contracts, and budgets.

About the Company

Precision for Medicine

Global CRO for precision medicine trials

Precision For Medicine is a global clinical research organization (CRO) that helps life sciences companies run clinical trials from early to regulatory approval. It specializes in precision medicine, focusing on oncology, cell and gene therapy, and rare diseases. The company combines clinical trial services with specialty laboratory work and data sciences to improve speed, reduce costs, and increase the likelihood of success in bringing therapies to patients. It differentiates itself by integrating advanced technologies and data-driven biostatistics with specialized labs to support end-to-end trials across all stages. Its goal is to enable faster, more cost-efficient development of targeted therapies that meet regulatory requirements and reach patients in need.

Company size
1,001-5,000
Company stage
Growth Equity (Venture Capital)
Total funding
$225M
Headquarters
Bethesda, MD
Founded
2012

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