Job Description
Schedule : Full-time Perform single case medical assessment, including the determination of seriousness, expectedness / listedness /labeledness, and causality of adverse events in compliance with current regulations, internal and external guidance documents, Standard Operating Procedures, Safety Job Aids, the Argus User Reference Guide and case processing/coding conventions.
Maintain the timely submission of expedited reports.
Support the achievement of the Therapeutic Areas case processing performance timelines. Identify cases that meet SUSAR reporting criteria, prepare the SUSAR narrative, perform risk assessment, initiate the unblinding process (as appropriate), and make the report available for distribution.
Identify and evaluate safety signals based on individual cases and cumulative data assessment and by using other signal detection systems. Provide data-driven decisions and communicate these findings proactively and effectively to the key stakeholders.
Partner with Worldwide Safety Strategy and with other Worldwide Safety and Regulatory Safety Operations functional groups to monitor the safety profile of assigned products.
Actively participate in Risk Management Committees and other risk management activities for assigned therapeutic areas. Perform product safety reviews as appropriate.
Provide medical safety input as appropriate to Clinical Development Teams regarding expectedness /listedness/labeledness, causality, and data reconciliation.
As appropriate, provide medical safety input, and review or draft sections of response documents to health authority inquiries.
Work with the Therapeutic Area Head to proactively and effectively communicate product safety issues and proposed solutions to PSSR management and to the Office of the EU Qualified Person.
Desired Profile
Medical Degree from an accredited
institution Minimum of two years of experience as an MD in clinical
practice Minimum of two years of relevant experience in
pharmacovigilance, clinical research or related field
Pharmaceutical industry experience preferred Working knowledge of
international regulations and guidance documents as related to worldwide
reporting requirements, preparation of clinical trial safety
assessments, and regulatory submissions including the preparation of
aggregate reportsEducation:UG -B.Sc - Any Specialization
PG - M.Sc - Any Specialization
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