Interpreting new legal and regulatory requirements relating to us data protection and privacy impacting businesses. In collaboration with the global program team, provide guidance to regional and business leads for implementation of identified requirements. Provide legal advice on testing and response for high risk implementation activities as appropriate.
Manage clinical study personnel focused on conducting clinical programs consistent with applicable regulations, guidelines, and policies. Interprets and executes on policies and procedures appropriate to clinical programs under his/her management. Recommends modifications to policies and procedures to larger clinical organization as necessary.
Develop and maintain strategies and initiatives that are in line with site culture. You also develop, implement and enforce incident prevention and regulatory compliance policies and procedures as required by site specific needs, regulations and corporate requirements.
Provide hands-on technical support for hardware (printers, barcode readers, cameras, desktop, laptop, drivers, monitors, mhds, and cabling) and software (internally developed applications, productivity, computer operating systems, internet applications, and various drivers) troubleshooting.
Responsible for planning, initiating, monitoring, tracking and/or prioritizing projects across various stages of the product life cycle (r&d, clinical research, surveillance) and for facilitating successful, on-time and within budget execution.