Job Description

• Participates in patient recruitment ensuring proper informed consent, eligibility requirements are met and enrolls patient onto trial
•  Inform study participants about the objective of the study
• Maintains compliance with protocol requirements and all applicable regulatory functions
• Monitor research subjects to ensure compliance to study rules
• Manages, monitors and reports research data
• Identifies, reviews, and reports adverse events, protocols deviations, and other unanticipated problems appropriately
• Performs administrative and regulatory duties related to study
• Ensue the necessary supplies and equipment are in stock
• Liaising with laboratories regarding findings
• Attends required training, maintains applicable certifications and/or licensure as required

Qualifications

• Ability to perform tasks with a high degree of accuracy
• Ability to work in multiple software programs/applications
• Ability to manage confidential information
• Excellent communication skills with patients, physicians, and staff

Minimum Education and Experience Requirements  

• 1 to 2 years of clinical research experience or extensive ophthalmic background
• Preferred: Bachelor’s Degree

Additional Information

information will be kept confidential according to EEO guidelines.