On assignment to Pfizer, Inc as a Site Monitor

Provide support to sites and CRAs directly to process and resolve queries and requests as needed. Serve as primary in-house contact for sites and investigators participating in studies. Become familiar with the principles of and assist with investigator recruitment. Conduct and complete remote site management activities, with support as needed, according to applicable SOPs and the Study Monitoring Plan. Contact clinical sites for specific requests, including enrollment updates, missing documentation, data entry timeliness, data query follow-up, CDA finding follow-up, and action item resolution or other sponsor specific tasks.