Clinical Trial Manager

This is a fully remote position, open to applicants in United Kingdom, +6 more countries.

📋 Description

• Oversee and operationally implement clinical components within trials, which includes site selection, initiation, enrollment management, site engagement and support, planning and executing monitoring, data cleaning, and trial closure.

• Successfully execute assigned trials and ensure all trial deliverables are met.

• Facilitate effective communication, manage regulatory documentation, and maintain ongoing oversight of assigned trials in collaboration with functional team members.

• Provide mentorship and training to team members.

• Identify potential challenges to study timelines and deliverables, and propose innovative action plans to the team or sponsor.

• Guide CRAs in fostering site relationships while overseeing monitoring, regulatory compliance, investigational product management, site payments, and correspondence activities.

• Keep the team focused on study priorities by fostering cross-functional partnerships and communication to achieve client satisfaction.

⛳️ Requirements

• A Bachelor's degree or an equivalent combination of education and experience in a science or health-related field, with specific experience in oncology.

• Proven experience in leading clinical aspects of studies across multiple countries within a CRO, Pharma, or Biotech company in a dedicated clinical lead role.

• Extensive clinical trial management experience in the field of oncology.

• Strong understanding of GCP/ICH guidelines and the clinical development process.

• Willingness to travel domestically and internationally, including overnight stays.

• Proficient in communicating effectively in the English language.

• Demonstrated computer skills in MS Office, MS Project, and PowerPoint.

• Experience with software such as CTMS, eTMF, EDC, and IXRS.

• Familiarity with medical terminology and clinical trial activities related to executing a clinical development plan.

• Comprehensive understanding of ICH-GCP, Precision SOPs, and regulatory guidance.

• Candidates must possess legal authorization to work in the country of employment without employer sponsorship.

🏝️ Benefits

• Flexible remote work arrangement.

• Opportunities for domestic and international travel, including overnight stays.

• Support for professional growth through mentoring and training opportunities.