• Assist with survey design, questionnaires, and sampling to meet client objectives • Act as the day-to-day contact for clients and project collaborators • Coordinate and manage multiple projects at once, ensuring on-time and accurate delivery • Partner with suppliers when needed to ensure high-quality data collection at reasonable costs • Analyze and interpret final datasets, creating clear, visually engaging reports (PowerPoint or similar) • Guide clients through findings using YouGov’s analytics tools and software

• Assist with survey design, questionnaires, and sampling to meet client objectives • Act as the day-to-day contact for clients and project collaborators • Coordinate and manage multiple projects at once, ensuring on-time and accurate delivery • Partner with suppliers when needed to ensure high-quality data collection at reasonable costs • Analyze and interpret final datasets, creating clear, visually engaging reports (PowerPoint or similar) • Guide clients through findings using YouGov’s analytics tools and software

• Advance AbbVie's pipeline by striving for excellence in clinical research, turning science into medicine for our patients and leveraging new advanced capabilities to drive industry leading performance. • Partners with the investigator and site staff for meaningful and effective engagements positioning AbbVie as the choice in clinical trials. • Focus on site clinical research that ensures appropriate conduct of the trial while driving improvement in data integrity, compliance, overall study performance and customer experience. • Conducts site evaluation, site training, routine, and site closure monitoring activities with compliance to the protocol and monitoring plans, in accordance with applicable regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), and quality standards, ensuring safety and protection of study subjects. • Gather local/site insights and utilize site engagement tools such as the Customer Relationship Management (CRM) tool, to report/track progress and measure impact of that strategy. • Evaluate and ensure effective recruitment and retention techniques/plans based on the patient disease journey. • Responsible for continuous risk-assessment proactively, and in collaboration with Central Monitoring team, monitor activities conducted by clinical sites to detect early overall study performance or patient safety issues.

• Performs on-site or remote Pre-Study, Initiation, Interim, and Close-Out monitoring visit activities to ensure that facilities and staff at the investigational site continue to be adequate for the conduct of the study • Identifies the investigators and verifies that the investigator has adequate qualifications, resources, facilities, equipment and staff to conduct the clinical study throughout the study period • Trains investigational site staff as necessary • When applicable, supports preparation of regulatory and / or EC submissions • Participates in mentoring/training of new staff as well as performing co-monitoring visits, to assess junior staff performance.