Novotech Global

Lead the end-to-end delivery of global clinical trials from start-up to close-out, ensuring compliance with ICH-GCP and company SOPs. Manage sponsor relationships, project budgets, and cross-functional teams to ensure studies are delivered on time and within budget.

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 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.