Clinical Research Associate

Responsibilities for Clinical Research Associate (CRA):

• Oversee multiple global clinical trials at a time through pre-study visits, close out visits, monitoring visits, and initiation visits.
• Monitor all documentation for the site including auditing for regulatory compliance including, but not limited to, informed consent documents and case report forms.
• Review compliance to protocols, document any deviations, and follow up with sites on corrective actions.
• Complete trip reports and review trip reports of junior Clinical Research Associates.
• Attend and participate in client meetings, kick off meetings, and investigator meetings.
• Oversee CRO

Technical Requirements for Clinical Research Associate (CRA):

• Bachelor’s Degree in biology, public health, nursing, or related field.
• At least 8 years of independent monitoring for CRO or Pharma
• Excellent written, verbal, communication, and organizational skills
• Ability to travel up to 70% regional travel,