Performs and coordinates all aspects of the clinical site monitoring services, assessing for protocol and regulatory compliance. Responsibilities include driving investigative site and patient recruitment, conducting source data verification, assessing drug accountability, data collection, (regulatory) document collection, performing qualification, initiation, monitoring and close out visits at investigational sites in accordance with corporate, sponsor and regulatory (ICH GCP and other) standards and guidelines. Represents the corporation by maintaining collaborative relationships with stakeholders.

QUALIFICATIONS

• Undergraduate university degree (Bachelor or Honors Bachelor), & 1-3 years’ related experience with initial and On-going training.

OR

• College Diploma/Degree, & 4-6 years related experience +substantial on-going job-related training.

Please refer the Job description for details