Screening QC Reviewer

Specific Tasks:

• Responsible for the reception, classification and processing of the biomedical analysis reports, including screening, retests, post-study and follow-up.
• Ensure the prompt gathering of documents in the screening record department: ECG, lab results, medical records, blood donations or others, including the hard copy of electronic updates of individual medical histories.
• Responsible for the verification of the volunteer’s medical history, and all other data recorded on the screening record.
• Responsible for the expedition of QC screening records at minimum 48 hours prior to day 0 of study.
• Responsible for the processing of transferred screening records to a new study.
• Responsible for the verification of all data collected during the return visits: arrival of volunteers, health questionnaire, Adverse Events, blood sampling, post-study lab reports, vital signs, ECG, Exam, centrifugation document, sorting document, shipping slip.

Qualifications:

Education: DEC or BAC with at least 1 year of experience in a clinical research environment.  Knowledge of GCP standards is a must.

Skills: Must possess organizational skills, attention to details, patience and autonomy. Written and spoken English and French are essential.

Software: MS-Office, Outlook, Dynamic’s Great Plain.