Considered as the primary point of contact for the investigative site.

High level of competency or experience in providing contextual information on the clinical trials, connects stakeholder to the investigative sites and strengthens AbbVie’s positioning.

Aligns, trains and motivates the site staff and principal investigator on the goals of the clinical trial program, protocol and patient treatment principles for the trial ensuring a trusted partnership.

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.

Advanced understanding of site engagement and ability to customize site engagement strategy for assigned study(ies).

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.

Advanced level of competency connecting the study protocol, scientific principles and clinical trial requirements to the day-to-day clinical trial execution activities.

Evaluate and ensure effective recruitment and retention techniques/plans based on the patient disease journey.

Develop solid knowledge of therapeutic area, asset and clinical landscape / patient journey to enable successful patient recruitment and overall protocol compliance.

Possesses experienced level of competency to mentor and train less experienced CRAs on various aspects of work and provides input into their development.

May participate in global/local task forces and initiatives.

Responsible for activities as assigned by manager.

Clinical Research Associate II - Dermatology (Southern California)

Responsibilities

Benefits

Company

AbbVie

More roles at AbbVie