Clinical Trial Manager

6 hours, 2 minutes ago
Full-time
Senior
Project and Program Management
Precision For Medicine

Precision For Medicine

Precision for Medicine is a specialized scientific services company that helps pharmaceutical and life sciences clients innovate, develop, and commercialize next-generation medical products. With a diverse team of experts, they offer comprehensive serv...

Pharmaceuticals
1K-5K
Founded 2012
$225M raised

Description

  • Manage the clinical and operational delivery of assigned trials, including site selection, startup, enrollment management, monitoring, data cleaning, and closeout.
  • Serve as the central point of coordination for study activities and oversee clinical aspects across multiple countries.
  • Lead CRAs and support high-quality oversight of monitoring, regulatory, investigational product, site payment, and site correspondence activities.
  • Ensure trial deliverables are completed on schedule and within scope.
  • Coordinate closely with cross-functional team members to maintain appropriate communication and regulatory documentation oversight.
  • Identify risks and timeline threats, and develop creative action plans to address study issues.
  • Mentor and train team members to support ongoing growth and performance.
  • Maintain team focus on study priorities and drive client satisfaction through effective communication and partnership.

Requirements

  • Bachelor’s degree or equivalent combination of education and experience in a science or health-related field.
  • Experience in oncology clinical trial management.
  • Demonstrable experience leading clinical aspects of studies across multiple countries in a CRO, pharma, or biotech setting in a dedicated clinical lead role.
  • Working knowledge of GCP/ICH guidelines and the clinical development process.
  • Availability for domestic and international travel, including overnight stays.
  • Ability to communicate effectively in English.
  • Demonstrated computer skills with MS Office, MS Project, and PowerPoint.
  • Experience with CTMS, eTMF, EDC, and IXRS systems.
  • Ability to build positive working relationships with internal and external organizations.
  • Strong understanding of medical terminology and clinical trial activities related to executing a clinical development plan.
  • Mastery knowledge of ICH-GCP, relevant Precision SOPs, and regulatory guidance, with ability to implement them.

Benefits

  • Remote work available in the UK, Hungary, Poland, Romania, Serbia, or Slovakia.
  • Opportunity to work on precision medicine and oncology studies with advanced biomarker and data analytics solutions.
  • Role with significant autonomy, ownership, and influence over how clinical trials are run.
  • Chance to work in a dynamic environment and contribute to high-impact research for patients worldwide.

Interested in this position?

Apply directly on the company website

Apply Now

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