Clinical Research Associate
Core
Partner with study teams, investigators, and site staff to ensure appropriate conduct of clinical trials, driving improvement in data integrity, compliance, and overall study performance.
Role type
Senior IC Clinical Research Associate (Site Management & Monitoring)
Builds
Clinical trial execution and data integrity for AbbVie's pipeline
Domain
Biopharmaceuticals / Clinical Research
Deliverable
physical/clinical work
Required skills
Site evaluation and qualification, On-site and off-site monitoring, Protocol compliance, Patient recruitment and retention, Risk assessment and mitigation, Data quality assurance, Regulatory inspection readiness, Investigator relationship management
Preferred skills
Mentorship of junior CRAs, Strategic site engagement, Therapeutic area expertise
Technologies
Clinical trial management systems, Site engagement tools
Responsibilities
Conduct site evaluation, training, routine monitoring, and closure activities; Ensure data quality and timely submission including safety event reporting; Manage investigator payments and negotiate agreements; Identify and recommend potential investigators/sites; Lead or participate in global/local task forces; Mentor and train less experienced CRAs.
Seniority
Senior, hands-on IC with mentorship responsibilities