Provide medical expertise and judgment throughout the case-handling process with medical review of individual cases.
Maintain knowledge of the marketed drug currently under litigation.
Take responsibility for appropriate capturing and coding of adverse events from the source.
Determine medically important events.
Resolve queries relating to drug coding.
Resolve queries relating to AE coding in MedDRA
Solve the medical queries during the case handling by case handlers.
Provide missing causality for clinical trial and solicited cases.
Provide seriousness assessment.
Employement Category:
Employement Type: Full timeIndustry: Bio Technology & Life SciencesFunctional Area: PharmaceuticalRole Category: Drug Regulatory DoctorRole/Responsibilies: Medical Reviewer Role For Qualifed- Mbbs/md With Mci In Nonclinical & Rotational Shifts