Clinical Trial Manager

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

📋 Description

• Oversee and operationally implement clinical components within trials, including site selection, initiation, enrollment management, site engagement and support, monitoring planning and execution, data cleaning, and close-out.

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

• Guarantee effective communication, regulatory documentation, and ongoing oversight of assigned trials in partnership with cross-functional team members.

• Provide mentorship and training to team members.

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

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

• Keep the team focused on study priorities through cross-functional collaborations and effective communication to ensure client satisfaction.

⛳️ Requirements

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

• Proven experience leading clinical aspects of studies across multiple countries in a Contract Research Organization (CRO), Pharmaceutical, or Biotech company in a dedicated clinical lead role.

• Extensive clinical trial management experience in oncology.

• Proficient understanding of Good Clinical Practice (GCP)/International Conference on Harmonisation (ICH) guidelines and the clinical development process.

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

• Must possess effective communication skills in English.

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

• Experience with Clinical Trial Management Systems (CTMS), electronic Trial Master Files (eTMF), Electronic Data Capture (EDC), and Interactive Voice Response Systems (IVRS).

• Demonstrated ability to cultivate positive working relationships with both internal and external organizations.

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

• Comprehensive knowledge of ICH-GCP, relevant Precision Standard Operating Procedures (SOPs), and regulatory guidelines, with the capability to implement them.

• Candidates must be legally authorized to work in the country of employment without employer sponsorship.

🏝️ Benefits

• Remote work arrangement.

• Continued growth support.

• Mentoring and training opportunities.

• Equal Opportunity Employer.

• Reasonable accommodations available for the application process.