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Why You'll Love This Job

The study coordinator will be responsible for a variety of clinical procedures including subject recruitment and follow-up, detailed record keeping and regulatory compliance, and correspondence with investigators, IRBs, and regulatory authorities.

Responsibilities

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