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Clinical Trial Manager

1 month, 2 weeks ago
Serbia, Slovakia, United Kingdom, Hungary, Poland, Romania
Full-time
Senior
Project Manager
Project and Program Management
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 79

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.
  • Serve as the central point of coordination for assigned studies and oversee all clinical aspects across multiple countries.
  • Lead CRAs and support high-quality site oversight, including monitoring, regulatory, investigational product, site payment, and site correspondence activities.
  • Ensure trial deliverables are completed on time and within scope.
  • Collaborate closely with cross-functional team members to maintain appropriate communication and regulatory documentation.
  • Identify risks and challenges to study timelines and deliverables and develop creative action plans.
  • Mentor and train team members.
  • Maintain team focus on study priorities through effective communication and cross-functional partnerships to support 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, pharma, 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.
  • Must be able to communicate effectively in English.
  • Demonstrated computer skills with MS Office, MS Project, and PowerPoint.
  • Software experience with CTMS, eTMF, EDC, and IXRS.
  • Demonstrated 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 knowledge of ICH-GCP, Precision SOPs, and regulatory guidance, with the ability to implement them.

Benefits

  • Remote work flexibility in the UK, Hungary, Poland, Romania, Serbia, or Slovakia.
  • Opportunity to work on precision medicine and oncology trials with a leading CRO.
  • Support for continued growth, including mentoring and training.
  • Equal Opportunity Employer workplace policies.
  • Reasonable accommodation support for applicants with disabilities.

Interested in this position?

Apply directly on the company website

Apply Now

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