Clinical Trial Manager

📋 Description

• 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.
• 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.
• Mentoring and training of team members.
• Identify challenges to study timelines/deliverables and offer creative action plans to the team/sponsor.
• Lead CRAs as they establish relationships with their sites for high quality oversight of monitoring, regulatory, IP, site payment and overall site correspondence activities.

🎯 Requirements

• Bachelor’s degree or equivalent combination of education/experience in science or health-related field, including experience in oncology.
• Demonstrable experience leading clinical aspects of your 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.

🎁 Benefits

• Remote work options and flexible schedule.
• Opportunity to work across multiple countries and global teams.
• Collaborative, fast-paced work environment with a focus on oncology and precision medicine.