Experienced Clinical Site Activation Specialist with over 2.5 years of experience in clinical operations and site management. Expertise lies in streamlining the site activation process, ensuring compliance with regulatory requirements, and facilitating efficient study start up
Assist team in the preparation, handling, distribution, filing and archiving of documentation according to the scope of work and standard operating procedures
IQVIA IMPACT SPOTLIGHT AWARD
Issued by IQVIA · Nov 2022
For contributions in CTMS Contacts and Accounts management (CCAM) process.
Clinical Research
Regulatory Compliance
Project Management
Clinical Trial Operations