Clinical Trial Manager
This role is a key part of our clinical research team, responsible for the oversight and management of clinical trials. The Clinical Trial Manager will work closely with cross-functional teams to ensure successful study execution, patient safety, and compliance with regulatory requirements.
Responsibilities:
* Manage site interactions post-activation through site closeout, ensuring timely completion of operational activities.
* Identify critical data and process risks, and develop risk mitigation strategies to ensure successful trial conduct.
* Oversee resourcing allocations for CRAs and Central Monitors, site assignments, and study team members' conduct.
* Review project oversight dashboards and other clinical trial systems to oversee site and patient activities, study team conduct, and ensure data integrity.
Requirements:
* Bachelor's degree in a related field or equivalent combination of education, training, and experience.
* Previous clinical trial experience in site management, with a focus on risk-based monitoring and clinical or central monitoring.
* Familiarity with financial principles and budget management practices.
* Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements.
* Strong communication, presentation, and interpersonal skills among project team and with sites.
Benefits:
* Moderate travel opportunity, approximately 20%.
* Opportunity to work with a leading biopharmaceutical solutions organization, accelerating customer success.
* Continuous learning and development opportunities.