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Precision Medicine Group

Biomarker-driven clinical development services and consulting

Senior Clinical Project Manager - Oncology

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeRemote in Poland

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 in a Clinical Operations position within a CRO, including at least four years of full-service project management experience in a clinical trial setting for a Clinical Research Organisation.
  • Experience managing Oncology studies.
  • 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 spoken and written English.
  • Strong presentation skills.
  • Computer skills with Microsoft Office, Microsoft Project, and PowerPoint, and software experience with CTMS, eTMF, EDC, and IXRS.
  • 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; may run international trials.
  • Serve as the primary point of contact and liaison with the client, including participating in proposal activities and client presentations.
  • Liaise with the Project Team and senior management at Precision and sponsors, 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, performance metrics, and escalation needs.
  • Contribute as an active member of the Project Team to efficient management and execution of trials.
  • Prepare and review protocols and other study documentation, including project plans, informed consents, site contracts, and budgets.
  • Provide full-service oversight for global and regional Phase I–IV clinical projects in Oncology, ensuring delivery against agreed timelines, scope, cost, and quality.
  • Participate in proposal strategy, development, costing, and bid defense, and manage studies through completion while overseeing client relationships, project teams, budgets, and timelines.
  • Drive quality and coordinate the study team across internal and external stakeholders.

About the Company

Precision Medicine Group

Biomarker-driven clinical development services and consulting

Precision Medicine Group provides specialized life sciences services to pharma and biotech companies across the full product lifecycle, from preclinical work to post-launch commercialization. Its Precision for Medicine unit runs biomarker assays, supports cell and gene therapy logistics through Project Farma, and manages global clinical trials, with ApoCell bolstering biomarker sample collection and analysis. The company differentiates itself by offering an integrated, biomarker-centric platform that combines scientific services with regulatory support and market access under one umbrella. Its goal is to de-risk and accelerate development and commercialization of targeted therapies by identifying responsive patient populations and demonstrating value to payers.

Company size
1,001-5,000
Company stage
Acquired
Total funding
$310.2M
Headquarters
Bethesda, MD
Founded
2012

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