• 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.

• You will be dedicated to a single client. • You will be responsible for all site management and supervisory activities in the assigned oncology studies. • You will work with industry leaders and subject matter experts. • You will have the opportunity to mentor junior CRAs. • You will work with world-class technology. • You will have great opportunities to travel, work from home, meet new people and play a key role in the drug development process.

• The CRA works in close collaboration with other CRAs and the Local Study Team to ensure that study commitments are achieved in a timely and efficient manner • Acts as the main contact with the study site and has the responsibility for monitoring study conduct • Responsible for the preparation, initiation, monitoring, and closure of assigned sites in clinical studies • Confirms that site staff have completed and documented the required training appropriately, including ICH-GCP training • Ensures that all study documents under their responsibility are available and ready for final archiving • Collaborates with local Medical Science Liaisons as directed by LSAD or line manager