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Clinical Trial Manager

5 hours, 41 minutes ago
Serbia, Slovakia, United Kingdom, Hungary, Poland, Romania
Full-time
Senior
Project Manager
Project and Program Management
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 operational delivery of clinical trial activities, including site selection, start-up, enrolment management, monitoring planning and execution, data cleaning, and close-out.
  • Lead CRAs and oversee clinical aspects of assigned studies across multiple countries.
  • Ensure trial timelines, scope, and deliverables are met with high-quality execution.
  • Coordinate regulatory documentation and ongoing oversight in collaboration with cross-functional team members.
  • Mentor and train team members supporting the study.
  • Identify risks and delivery challenges, and develop creative action plans for the team and sponsor.
  • Maintain strong site relationships and oversee monitoring, regulatory, investigational product, site payment, and site correspondence activities.
  • Drive cross-functional communication and partnerships to maintain study priorities and client satisfaction.

Requirements

  • Bachelor’s degree or equivalent combination of education and experience in a science or health-related field.
  • Experience in oncology, including significant clinical trial management experience in oncology.
  • Demonstrable experience leading clinical aspects of studies across multiple countries in a CRO, pharmaceutical, or biotech company 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.
  • Strong English communication skills.
  • Demonstrated computer skills with MS Office, MS Project, and PowerPoint.
  • Experience with clinical trial systems such as CTMS, eTMF, EDC, and IXRS.
  • Ability to develop positive working relationships with internal and external organizations.
  • Core understanding of medical terminology and clinical trial activities related to execution of a clinical development plan.
  • Mastery knowledge of ICH-GCP, relevant 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 a specialized CRO.
  • Role within a growing team focused on novel clinical trial designs and advanced data analytics.
  • Chance to contribute to research aimed at improving patient outcomes worldwide.

Interested in this position?

Apply directly on the company website

Apply Now

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