• To plan and execute the logistics of the Bioequivalence/Dermatological/Personal Healthcare clinical studies.
• IEC/IRB single point contact coordinator attended IEC/IRB protocols review meeting and obtained approved protocol for clinical study conduct and shared IEC/IRB approved protocols with team, Investigators and Sponsor.
• To develop various essential Standard Operating Procedures (SOPs) in consultation with investigators/Director-Global Clinical Operations.
• To verify that the technical study staff including the investigators, are conducting the study according to the clinical trial protocol and as per the standards laid down in the in-house SOPs, Good Clinical Practic...