Clinical Research Associate (CRA) - Colorado

Location

Colorado-wide, United States

Salary

Not specified

Company

Akash pawar

Job description

• Role & Company / Project Overview Mindlance is recruiting Clinical Research Associates (CRAs) in Colorado to support West Coast regional clinical research programs. • Key Responsibilities & Daily Duties - Carry out independent onsite monitoring across clinical trial sites. - Drive deliverables and manage site interactions independently. - Maintain rigorous GCP compliance throughout the trial lifecycle. • Required Qualifications, Skills & Experience - Minimum 2+ years of independent, onsite clinical monitoring experience. - Practical experience managing clinical trial sites and deliverables independently. - Strong comprehension of clinical trial monitoring methodologies and GCP compliance. - Exposure to oncology, neurology, ophthalmology, or rare disease therapeutic areas is a plus. • Working Hours, Shifts & Location Details - Location: Colorado, United States. - Travel: Up to 80% travel required. • Compensation & Benefits - Not specified. • Application Instructions - Please submit your updated resume via email.