Clinical Research Associate (CRA) - Arizona

Location

Arizona-wide, United States

Salary

Not specified

Company

Akash pawar

Job description

• Role & Company / Project Overview Mindlance has open CRA opportunities in Arizona, part of the West Coast region clinical trials operations. • Key Responsibilities & Daily Duties - Execute independent onsite monitoring visits to clinical trial sites. - Independently manage trial sites and fulfill monitoring deliverables. - Verify adherence to clinical study protocols and GCP compliance. • Required Qualifications, Skills & Experience - Minimum 2+ years of independent, onsite clinical monitoring experience. - Proven ability to manage clinical trial sites and key monitoring milestones. - Solid knowledge of clinical trial monitoring and GCP guidelines. - Experience in therapeutic areas like oncology, neurology, ophthalmology, or rare disease is a plus. • Working Hours, Shifts & Location Details - Location: Arizona, United States. - Travel: Flexibility to travel up to 80%. • Compensation & Benefits - Not specified. • Application Instructions - Send an updated resume via email to apply.