Clinical Trial Manager

This is a fully remote position, open to applicants in Slovakia, +4 more countries.

📋 Description

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

• Successfully execute assigned trials and ensure the fulfillment of trial deliverables.

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

• Provide mentorship and training to team members.

• Recognize challenges related to study timelines and deliverables, and propose innovative action plans to the team and sponsor.

• Guide CRAs in building site relationships and supervising activities related to monitoring, regulatory compliance, investigational product management, site payments, and site correspondence.

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

⛳️ Requirements

• 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 leading clinical aspects of studies across multiple countries within a CRO, Pharma, or Biotech organization in a dedicated clinical lead position.

• Extensive clinical trial management experience in oncology.

• Sound knowledge of GCP/ICH guidelines and the clinical development process.

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

• Proficient in effective communication in English.

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

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

• Proven ability to establish positive working relationships with both internal and external organizations.

• Solid understanding of medical terminology and clinical trial activities associated with the execution of clinical development plans.

• Expertise in ICH-GCP, Precision SOPs, and regulatory guidelines, with the ability to implement them effectively.

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

🏝️ Benefits

• Opportunity for remote work.

• Support for professional growth and ongoing development.

• Equal Opportunity Employer.