Clinical Trial Manager

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

📋 Description

• Oversee and operationally implement clinical components within trials, encompassing site selection, start-up, enrollment management, site engagement and assistance, monitoring planning and execution, data cleaning, and close-out.

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

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

• Provide mentorship and training to team members.

• Recognize potential challenges to study timelines and deliverables, and devise innovative action plans for the team or sponsor.

• Lead Clinical Research Associates (CRAs) in managing site relationships and overseeing monitoring, regulatory, investigational product, site payment, and site correspondence activities.

• Maintain study priorities through cross-functional collaboration and communication to ensure client satisfaction.

• Act as the central intelligence hub for managed studies and supervise clinical aspects across multiple countries.

⛳️ Requirements

• Bachelor’s degree or an equivalent combination of education and experience in a science or health-related field, including oncology experience.

• 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, particularly in oncology.

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

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

• Proficient communication skills in English.

• Competent in using MS Office, MS Project, and PowerPoint.

• Familiarity with CTMS, eTMF, EDC, and IXRS software.

• Knowledge of medical terminology and clinical trial activities related to executing clinical development plans.

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

• Experience with CAR-T therapies and radiopharmaceuticals will be considered a significant advantage.

🏝️ Benefits

• Opportunity to work remotely from Hungary, Poland, Romania, Serbia, Slovakia, the UK, or Spain.

• Regular full-time employment.

• Opportunities for domestic and international travel.

• Support for mentoring and training.

• Commitment to equal opportunity employment.

• Reasonable accommodation support for applicants with disabilities.