Duties include:• Liaise with sponsors and multi-disciplinary study teams to develop monitoring plans• Assist in the development of study protocols• Perform on-site monitoring of studies to sponsor and protocol requirements• Source data verification, drug accountability and interpret/analyse study records and procedures• Write and submit monitoring reports to sponsor• Conduct formal closure of study centres on trial completion (close-out visits)• Facilitate and… Show more Duties include:• Liaise with sponsors and multi-disciplinary study teams to develop monitoring plans• Assist in the development of study protocols• Perform on-site monitoring of studies to sponsor and protocol requirements• Source data verification, drug accountability and interpret/analyse study records and procedures• Write and submit monitoring reports to sponsor• Conduct formal closure of study centres on trial completion (close-out visits)• Facilitate and participate in internal audits• Participate in trial management team and trial management group meetings Show less

Duties included:• Dispensing and packaging investigational medicinal products• Performing pharmacy inventories• Receiving and sending product shipments• Taking part in sponsor and client tours and meetings• Accommodating regulatory authority inspections (FDA and MHRA)• Installing, maintaining and managing clinic and pharmacy equipment

Duties included:• Collecting and handling biological substances such as blood and urine• Processing of blood using accurate pipettes and centrifuges• Collecting and interpreting source data• Measuring study participants’ vital signs and ECGs• Interpreting clinical study protocols• Responding to study participants’ needs