Clinical Trial Manager

This is a fully remote position, open to applicants in Poland.

📋 Description

• Oversee and manage the clinical components of a trial, which includes site selection, initiation, enrollment management, site engagement and support, monitoring planning and execution, data cleaning tasks, and trial close-out.

• Ensure the successful execution of assigned trials, guaranteeing the completion of all trial deliverables.

• Facilitate effective communication, manage regulatory documentation, and provide continuous oversight of assigned trial(s) by collaborating closely with other functional team members.

• Provide mentorship and training to team members.

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

• Lead Clinical Research Associates (CRAs) as they build relationships with their sites to ensure high-quality oversight of monitoring, regulatory compliance, investigational product (IP) management, site payments, and overall site correspondence.

• Maintain team focus on study priorities through efficient cross-functional collaborations and effective communication to achieve maximum client satisfaction.

⛳️ Requirements

• A Bachelor’s degree or equivalent in a science or health-related field.

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

• Extensive clinical trial management experience, particularly in oncology.

• Familiarity with GCP/ICH guidelines and the clinical development process.

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

• Proficient communication skills in the English language.

🏝️ Benefits

• Health insurance.

• Retirement plans.

• Flexible work arrangements.

• Opportunities for professional development.