Job Overview: Assist with the overall Clinical Safety and/or PSS operations associated with products including the entire adverse events process which may include safety data collected from clinical trials and/or post marketing setting (i.e., unsolicited reports).
Job Overview: Manage ‘Client’ or ‘Project’ specific PSS operations associated with products including the entire adverse events process: which may include safety data collected from clinical trials and/or post marketing setting (i.e., unsolicited reports) for specified
What Youll Do: Assist in compilation and revision of Regulatory Affairs (RA) documents required for clinical trials submissions Assist in the contact with local study teams for RA documents collection and checks, when applicable Assist in