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Clinical Trial Manager

8 hours, 32 minutes ago
Serbia, Slovakia, United Kingdom, Hungary, Poland, Romania
Full-time
Senior
Program 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 109

Description

  • Manage the clinical and operational delivery of assigned trials, including site selection, start-up, enrollment management, monitoring, data cleaning, and close-out.
  • Lead CRAs and oversee clinical study activities across multiple countries.
  • Ensure trial timelines, scope, and deliverables are met while maintaining quality standards.
  • Coordinate regulatory documentation and ongoing study oversight with cross-functional team members.
  • Mentor and train team members supporting the study.
  • Identify risks and challenges to study timelines or deliverables and propose corrective action plans.
  • Build and maintain effective site relationships and support monitoring, regulatory, investigational product, site payment, and site correspondence activities.
  • Maintain focus on study priorities through cross-functional collaboration and clear communication to support client satisfaction.

Requirements

  • Bachelor’s degree or equivalent combination of education and experience in a science or health-related field, including oncology experience.
  • Significant clinical trial management experience in oncology.
  • Demonstrable experience leading clinical aspects of studies across multiple countries in a CRO, pharma, or biotech setting in a clinical lead role.
  • Working knowledge of GCP/ICH guidelines and the clinical development process.
  • Availability for domestic and international travel, including overnight stays.
  • Fluent or effective communication in English.
  • Demonstrated computer skills with MS Office, MS Project, and PowerPoint.
  • Experience using CTMS, eTMF, EDC, and IXRS systems.
  • Ability to develop 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 of ICH-GCP, relevant Precision SOPs, and regulatory guidance, with the ability to implement them.

Benefits

  • Remote work is available in the UK, Hungary, Poland, Romania, Serbia, or Slovakia.
  • Opportunity to work on precision medicine and oncology-focused clinical trials.
  • Join a growing team with exposure to complex, multi-country studies.
  • Work in an environment that supports autonomy, ownership, and professional growth.

Interested in this position?

Apply directly on the company website

Apply Now

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