Clinical Research Associate

Job description

The Position

This role will be responsible for providing coordination and support to all clinical operation team to ensure achievement of study goals, as well as tracking and maintaining study logistic information, systems and tools and appropriate study documentation.

Main Duties

• Conducting activities related to start-up, on-going and close down phase. Including delivering training, site management, monitoring and support.
• Reconciling and tracking essential documents for the country level Trial Master File
• Ensuring documentation and archiving for all clinical study documents
• Keeping databases/tracking systems/tools/study documents up to date
• Becoming co-monitor, as required and with appropriate oversight and training, during high volumes periods (e.g. initiation visit, document reconciliation at study close-out) or when appropriate, to alleviate back logs in study workload which could potentially have a negative impact in achieving project
• Developing and maintaining functional knowledge of GCPs, Roche SOP and Local Regulations and therapeutic area (s) through continued training to ensure patient safety and data integrity.

Who you are

• 2 year experience in clinical operations
• University degree in pharmacy or biology
• Good command of English
• Teamwork, detail management

Who we are

At Roche, more than 100,000 people across 100 countries are pushing back the frontiers of healthcare. Working together, we’ve become one of the world’s leading research-focused healthcare groups. Our success is built on innovation, curiosity and diversity.

Roche is an Equal Opportunity Employer.