Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company’s integrity & quality standards
Liaise with Global Regulatory Affairs, Medical, Clinical and Pharmacovigilance teams to obtain required documentation and ensure successful submissions.
Solid organizational skills with the ability to adapt and adjust to changing priorities and to manage multiple assignments with challenging/conflicting deadlines
SunGlow was incorporated in January 2010 and was founded by a group of experienced industry professionals. Our Corporate office is located in Chennai, India.
Design and evaluate oncology clinical trial frameworks — including study protocols, patient enrollment strategies, and regulatory compliance considerations