Clinical Research Associate (CRA) - Texas

Location

Texas-wide, United States

Salary

Not specified

Company

Akash pawar

Job description

• Role & Company / Project Overview Mindlance has openings for Clinical Research Associates (CRAs) in Texas within the Central region. The role is focused on managing clinical trial sites and fulfilling onsite monitoring responsibilities. • Key Responsibilities & Daily Duties - Conduct independent, onsite monitoring of clinical trials. - Manage clinical trial sites independently, tracking and meeting all monitoring deliverables. - Maintain high standards of GCP compliance throughout all monitoring engagements. • Required Qualifications, Skills & Experience - Minimum 2+ years of independent, onsite clinical monitoring experience. - Demonstrated capability in managing clinical trial sites independently. - In-depth understanding of clinical trial monitoring and GCP standards. - Prior experience in oncology, neurology, ophthalmology, or rare disease therapeutic areas is advantageous. • Working Hours, Shifts & Location Details - Location: Texas, United States (Central region). - Travel: Up to 80% travel required for onsite visits. • Compensation & Benefits - Not specified. • Application Instructions - Please submit your updated CV/resume via email to apply.