· Ensure subject safety at all times during the clinical study and after the study has been completed as required by the protocol and GCP and GLP regulations.

· Review study protocols to acquire in-depth knowledge of the protocol.

· Assist the Qualified Investigator in all duties regarding the safe conduct of clinical research.

· Carry out the full spectrum of medical activities related to subject eligibility for studies (medical exam, laboratory results, electrocardiogram assessment,…) so that inclusion and exclusion criteria are respected (pre-study).

· Perform follow-up and ensure the quality of information related to subject eligibility.

· Responsible for on-study supervision and works closely with clinical research staff.

· Perform all required clinical exams as per the study protocol.

· Assess adverse events and carry out the appropriate medical judgement, and follows-up to determine the resolution of adverse events.

· Interact with clients for onsite visits to address any safety concerns/questions.

· Participate in on-call coverage requirements.

· May be called upon to perform other duties as required.

Responsible for performing activities that are in compliance with applicable Corporate and Divisional Policies, Standard Operating Procedures and Operating Guidelines and performing other duties as assigned by management.

· Ensure subject safety at all times during the clinical study and after the study has been completed as required by the protocol and GCP and GLP regulations.

· Review study protocols to acquire in-depth knowledge of the protocol.

· Assist the Qualified Investigator in all duties regarding the safe conduct of clinical research.

· Carry out the full spectrum of medical activities related to subject eligibility for studies (medical exam, laboratory results, electrocardiogram assessment,…) so that inclusion and exclusion criteria are respected (pre-study).

· Perform follow-up and ensure the quality of information related to subject eligibility.

· Responsible for on-study supervision and works closely with clinical research staff.

· Perform all required clinical exams as per the study protocol.

· Assess adverse events and carry out the appropriate medical judgement, and follows-up to determine the resolution of adverse events.

· Interact with clients for onsite visits to address any safety concerns/questions.

· Participate in on-call coverage requirements.

· May be called upon to perform other duties as required.

Responsible for performing activities that are in compliance with applicable Corporate and Divisional Policies, Standard Operating Procedures and Operating Guidelines and performing other duties as assigned by management.