Management and operational delivery of the clinical elements within a trial including site selection, start-up, enrolment management, site engagement and support, monitoring planning and execution, data cleaning activities and close-out
Serve as the hub of central intelligence for assigned studies and lead CRAs across multiple countries to ensure timeline adherence and quality delivery
Successful execution of assigned trials and ensuring completion of trial deliverables
Ensure appropriate communication, regulatory documentation, and ongoing oversight of assigned trial(s) by working in close collaboration with other functional team members
Mentor and train team members
Identify challenges to study timelines/deliverables and offer creative action plans to the team/sponsor
Lead CRAs in establishing relationships with sites for high quality oversight of monitoring, regulatory, IP, site payment and overall site correspondence activities
Maintain team focus on study priorities through efficient cross-functional partnerships and effective communication to achieve the highest level of client satisfaction
Requirements
Bachelor’s degree or equivalent combination of education/experience in science or health-related field, including experience in the field of oncology
Demonstrable experience leading 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 the area of oncology
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 the English language
Demonstrated computer skills (MS Office, MS Project, PowerPoint) and software experience (CTMS, eTMF, EDC, IXRS)
Demonstrated ability to develop positive working relationships with internal and external organizations
Demonstrates core understanding of medical terminology and clinical trial activities
Demonstrates mastery knowledge of ICH-GCP, meaningful Precision SOPs, and regulatory guidance, as well as the ability to implement
Benefits
Candidates can work remotely in UK, Spain, Hungary, Poland, Romania, Serbia or Slovakia.
Support for continued growth and development
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.