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Clinical Trial Manager

8 hours, 33 minutes ago
Serbia, Slovakia, United Kingdom, Hungary, Poland, Romania
Full-time
Senior
Project Manager
Project and Program Management
GCP
Apply Now
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
View All Jobs 86

Description

  • Manage the clinical and operational delivery of assigned clinical trials, including site selection, start-up, enrolment management, site engagement and support, monitoring planning and execution, data cleaning, and close-out.
  • Serve as the central point of intelligence for assigned studies and oversee all clinical aspects across multiple countries.
  • Lead CRAs and support their oversight of monitoring, regulatory, investigational product, site payment, and site correspondence activities.
  • Ensure trial timelines, scope, quality, and deliverables are met.
  • Work closely with cross-functional team members to maintain appropriate communication, regulatory documentation, and ongoing study oversight.
  • Identify risks and challenges to study timelines or deliverables and develop creative action plans.
  • Mentor and train team members to support continued growth and delivery.
  • Maintain team focus on study priorities through effective cross-functional partnership and communication 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.
  • Significant clinical trial management experience in oncology.
  • Demonstrable experience leading clinical aspects of studies across multiple countries in a CRO, pharma, or biotech company 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.
  • Must be able to communicate effectively in English.
  • Demonstrated computer skills with MS Office, MS Project, and PowerPoint, plus experience with CTMS, eTMF, EDC, and IXRS.
  • Demonstrated ability to develop positive working relationships with internal and external organizations.
  • Core understanding of medical terminology and clinical trial activities as they relate 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 oncology and precision medicine studies with advanced biomarker and data analytics capabilities.
  • Equal Opportunity Employer environment.
  • Reasonable accommodation support for applicants with disabilities during the application process.

Interested in this position?

Apply directly on the company website

Apply Now

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