Senior Clinical Research Associate

Advance AbbVie 's pipeline by striving for excellence in clinical research, turning science into medicine for our patients and leveraging advanced capabilities to drive industry leading performance. Requirements Considered as the Primary Sponsor Point of contact for the investigative site. Ability to motivate and align monitoring community through leadership and mentorship. Conducts site evaluation, site training, routine on-site and off-site monitoring, 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. Possesses advanced level of competency to mentor and train less experienced CRAs on various aspects of work and provides input into their development. Independently Identifies, evaluates and recommends new/potential investigators/sites on an on going basis demonstrating expert understanding and decision making. Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel. Ensures audit and regulatory inspection readiness at assigned clinical site at all times. Benefits Paid time off (vacation, holidays, sick) Medical/dental/vision insurance 401(k) Originally posted on Himalayas