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Clinical Trial Manager

7 hours, 5 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 83

Description

  • Manage the operational delivery of clinical trial activities, including site selection, start-up, enrollment management, site engagement, monitoring, data cleaning, and close-out.
  • Oversee assigned trials to ensure completion of deliverables and adherence to timelines and scope.
  • Coordinate regulatory documentation and ongoing trial oversight in collaboration with cross-functional team members.
  • Lead and support CRAs in monitoring, regulatory, investigational product, site payment, and site correspondence activities.
  • Mentor and train team members to support ongoing development and trial execution.
  • Identify risks and challenges to study timelines and deliverables and propose creative action plans.
  • Maintain focus on study priorities through effective communication and cross-functional partnership to support client satisfaction.
  • Serve as a central point of coordination for studies managed across multiple countries.

Requirements

  • Bachelor’s degree or equivalent combination of education and experience in a science or health-related field.
  • Experience in oncology.
  • Demonstrable experience leading clinical aspects of studies across multiple countries in a CRO, pharmaceutical, or biotech company 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 systems.
  • Ability to build positive working relationships with internal and external organizations.
  • Strong understanding of medical terminology and clinical trial activities related to clinical development plans.
  • 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 trials.
  • Chance to join a growing team at Precision for Medicine.
  • Work in a role with significant autonomy and ownership.
  • Exposure to cross-functional, multinational clinical trial delivery.

Interested in this position?

Apply directly on the company website

Apply Now

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