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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 SlovakiaNo salary listed

About the Job

Requirements

  • A degree or similar related life science qualification, or an equivalent combination of education and experience, is required.
  • Previous experience in a full-service or global project management role in the contract research organization (CRO) industry is essential.
  • Extensive clinical operations experience within a CRO and at least four years of full-service project management experience in a clinical trial setting at a clinical research organization are required.
  • Experience managing oncology studies is required.
  • A working understanding of Good Clinical Practice (GCP) and International Council for Harmonisation (ICH) guidelines and the clinical development process is required.
  • The candidate must be able to drive and be available for domestic and international travel, including overnight stays.
  • Effective written and spoken English communication is required.
  • Strong presentation skills are required.
  • Proven computer skills in Microsoft Office, Microsoft Project, and PowerPoint, and software experience with clinical trial management systems (CTMS), electronic trial master files (eTMF), electronic data capture (EDC), and interactive response technology (IXRS) are required.
  • The candidate must be able to develop positive working relationships with individuals and teams internally and externally.
  • A core understanding of medical terminology and clinical trial activities as they relate to executing a clinical development plan is required.
  • Candidates must be legally authorized to work in the country of employment without employer sponsorship.

Responsibilities

  • Independently lead clinical projects in accordance with the study budget and scope of work, setting and achieving contracted and financial objectives; projects may include 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 of the company 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, success metrics, and escalation items.
  • Participate as an active project team member to contribute to the efficient management and execution of trials.
  • Prepare and review protocols and other study documentation, including project plans, informed consents, site contracts, and budgets.

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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