Clinical Lead II/III

Premier Research

United Kingdom

We’re looking for a Clinical Lead II/III - Oncology to join our Clinical Management team that is passionate about improving healthcare through innovative clinical research. As a member of the Premier Research team, you’ll help create tangible solutions for patients in need while building cross-functional partnerships that enable your growth and success.

What you’ll be doing:

  • Provides coaching and mentoring to clinical staff, study team and external stakeholders and act as Ambassador for Clinical Management Group to internal and external stakeholders;
  • Manage clinical portion of the trial in a patient centric approach and proactively identifying risk, potential patient safety events, and maintain oversight for data integrity;
  • Successfully oversee and monitor CRAs in a matrix environment with a focus on quality and timely deliverables; address issues with appropriate team and line manager; direct involvement in selection and activation of investigative sites; ensure the timely completion of all visit reports;
  • Drive the successful activation of trial sites according to time, quality/scope and budget parameters;
  • Plan and drive both patient recruitment and retention together with the project manager (PM), inclusive of preparing and executing a site and patient recruitment and retention plan/strategy to motivate recruitment in order to meet milestone;
  • Drive the clinical team forward to meet contractual milestones such as first site activated, first patient in, last patient in, and database lock;
  • Deliver and coordinate appropriate and timely training to the Premier clinical team and enlist therapeutic assistance where applicable to ensure the validity, correctness, and completeness of the clinical data;
  • Work with Project Management and Financial Analyst to accurately forecast clinical tasks including monitoring visits;
  • Actively participate in Bid Defense activities.

You’ll need this to be considered:

  • Bachelor’s degree, or its international equivalent from an accredited institution, in a clinical, biological, scientific, or health-related field;
  • 7 years+ of previous Clinical Oversight experience as a Clinical Lead;
  • 2 years + of onsite monitoring experience;
  • Rare Disease/Pediatrics experience is preferred;
  • Working knowledge of clinical financials including understanding of budgets, pass- through and resource management;
  • Experience on the CRO side is preferred;
  • Fluent verbal and written English as well as the local language(s) required;
  • Known for being customer-focused in approach to work and communications with the ability to professionally interact with sites;
  • Excellent organizational and time-management skills, able prioritize work to meet deadlines.

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