Key Responsibilities 1 To obtaining Inform Consent Form 2 To request and maintain accountability of all study related documents 3 To check all study related documents for its legibility accuracy and completeness 4 To solve QA RGA queries 5 To conduct study initiation meeting 6 To supervise all ongoing study procedures including screening check-in dosing blood collection and sample separation 7 To do check-in and check-out of subjects 8 To screen the subjects for participation in the Clinical Research study 9 To prepare issue and handle the identity cards of subjects 10 To prepare and display study information details 11 To supervise meal distribution 12 To supervise water and posture restriction 13 To participate in dosing procedure 14 To Compile Trial Master File 15 To operate and maintain breath alcohol analyzer 16 To manage subjects during study 17 To prepare study related labels 18 Any other administrative or system related activities has assigned by the Head- Clinical or PI 19 To check the raw data before Quality Assurance check 20 To monitor the Bio-Waste management 21 To make Entry in CRF Case record form 22 To handle the IMP 23 To participate in dosing procedure 24 To prepare study related labels for IMPs Other 25 Any other assigned work allotted by Group Leader Head Clinical PI 26 Report any areas of concern they have relating to the quality system to their line manager Directors QAU-Head 27 To prepare the work related SOPs Standard Operating Procedures and perform all activities as per SOP Standard Operating Procedures Job Type Full time Pay 15 000 00 - 20 000 00 per month Benefits Provident Fund Education Bachelor s Preferred Experience total work 1 year Preferred Location Sevasi Vadodara Gujarat Preferred Work Location In person

📌 Clinical Research Associate (Gujarat)
🏢 Anjna Hospital & Clinisearch Pvt.Ltd
📍 Gujarat