Novotech Global

The Clinical Research Associate is responsible for managing site relationships and ensuring clinical trials are conducted in accordance with ICH GCP guidelines and regulatory requirements. They monitor investigational sites to protect participant wellbeing and ensure trial data accuracy and completeness.

The Inhouse Clinical Research Associate provides support to the clinical team by managing study documentation, maintaining the Trial Master File, and ensuring compliance with regulatory requirements. They also assist with site management, investigator payments, and the coordination of trial materials to ensure project milestones are met.

The Associate Regulatory Start Up Manager plans, drives, and coordinates regulatory and start-up operational aspects across a region to ensure project deliverables meet client expectations. They also oversee submission processes to health authorities and ethics committees while managing risks and facilitating cross-functional team cooperation.