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Clinical Trial Manager

8 hours, 57 minutes ago
Serbia, Slovakia, United Kingdom, Hungary, Poland, Romania
Full-time
Senior
Project Manager
Project and Program Management
GCP
Apply Now
Precision Medicine Group

Precision Medicine Group

Precision Medicine Group specializes in precision medicine, utilizing targeted expertise and data insights to accelerate drug development and enhance the commercialization of next-generation medical products for the pharmaceutical and life sciences ind...

Pharmaceuticals
251-1K
Founded 2012
View All Jobs 106

Description

  • Manage the clinical and operational delivery of assigned trials, including site selection, start-up, enrolment management, monitoring, data cleaning, and close-out.
  • Serve as the central point of coordination for the studies you manage and maintain oversight of all clinical aspects across multiple countries.
  • Lead CRAs and support their relationships with sites to ensure quality monitoring, regulatory compliance, IP handling, site payments, and site correspondence.
  • Ensure trial deliverables are completed and that timelines, scope, and quality standards are maintained.
  • Coordinate closely with cross-functional team members to ensure appropriate communication, regulatory documentation, and ongoing trial oversight.
  • Identify risks, challenges, and threats to study timelines or deliverables and develop creative action plans.
  • Mentor and train team members to support continued growth and effective trial execution.
  • Maintain team focus on study priorities through effective communication and cross-functional partnership to maximize client satisfaction.

Requirements

  • Bachelor’s degree or equivalent combination of education and experience in a science or health-related field, including oncology experience.
  • Demonstrable experience leading clinical aspects of studies across multiple countries in a CRO, pharma, or biotech environment in a dedicated clinical lead role.
  • Significant clinical trial management experience in oncology.
  • 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 software systems.
  • Ability to develop positive working relationships with internal and external organizations.
  • Core understanding of medical terminology and clinical trial activities related to executing a clinical development plan.
  • Mastery knowledge of ICH-GCP, Precision SOPs, and regulatory guidance, with the 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 trials with advanced biomarker and data analytics capabilities.
  • Work in a role with autonomy, ownership, and responsibility for trial delivery.
  • Exposure to a dynamic, high-energy environment with opportunities to support continued growth and development.

Interested in this position?

Apply directly on the company website

Apply Now

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