Clinical Research Associate I - Oncology (Little Rock/Shreveport/Dallas)

📋 Description

• Considered as the primary point of contact for the investigative site, provides contextual
• Aligns, trains and motivates the site staff and principal investigator under supervision on the
• Conducts site evaluation, site training, routine, and site closure monitoring activities under
• Customize site engagement strategy for assigned study(ies) under supervision. Gather local/site
• Fundamental level of competency connecting the study protocol, scientific principles and clinical
• Responsible for continuous risk-assessment proactively, and in collaboration with Central

🎯 Requirements

• Appropriate tertiary qualification in health related disciplines (Medical, Scientific, Nursing)
• Clinically related experience, preferably in clinical research coordinating or data management.
• Knowledge of appropriate therapeutic area indications is preferred with the ability to understand
• Knowledge on existing and emerging local regulatory and legal requirements, ICH/GCP Guidelines and
• Able to work collaboratively and cross functionally to develop and sustain working relationships.
• Demonstrate planning and organizational skills and the ability to work effectively and efficiently

🎁 Benefits

• Comprehensive package of benefits including paid time off (vacation, holidays, sick)
• This job is eligible to participate in our short-term incentive programs.