Clinical Trial Manager

1 day, 8 hours ago
Full-time
Senior
Project and Program Management
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

Description

  • Manage the operational delivery of clinical trial activities, including site selection, start-up, enrolment management, site engagement, monitoring, data cleaning, and close-out.
  • Own the successful execution of assigned trials and ensure completion of trial deliverables.
  • Coordinate communication, regulatory documentation, and ongoing oversight of assigned studies with cross-functional team members.
  • Lead CRAs and support their relationships with sites to ensure high-quality monitoring, regulatory, IP, site payment, and site correspondence activities.
  • Mentor and train team members.
  • Identify risks, timeline challenges, and delivery issues, and propose creative action plans to address them.
  • Maintain team focus on study priorities through effective cross-functional collaboration and communication.
  • Ensure timeline adherence, scope control, and quality delivery across studies in multiple countries.

Requirements

  • Bachelor’s degree or equivalent combination of education and experience in a science or health-related field.
  • Experience in oncology, including experience in the field of oncology.
  • Demonstrable experience leading the clinical aspects of studies across multiple countries in a CRO, pharma, 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 software.
  • Ability to develop positive working relationships with internal and external organizations.
  • Core understanding of medical terminology and clinical trial activities as they relate to execution of a clinical development plan.
  • 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.
  • Join a growing team with responsibility and ownership in a high-impact role.

Interested in this position?

Apply directly on the company website

Apply Now

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