Accountable for the medical review of relevant clinical, other solicited and spontaneous cases
(including literature articles), medical assessment (including labeling and causality along with
the company causality statement)
Review the medical sense including seriousness and coding of the case in the global context of
the drug or clinical project, including the narrative, AE/SAE terms, suspect drugs, concomitant
medications, laboratory data, and medical history
Developing and maintaining thorough knowledge of the appropriate disease biology areas &
important safety concerns for marketed drugs and drugs in development
Assuring and maintaining compliance with regulatory and local/global SOP timelines
Supporting the Drug Safety teams with medical concepts and awareness of product related topics to ensure quality of adverse event data processing
Representing safety physician team in internal and client safety forums and audits
Review and respond to any queries/comments for an individual case safety report in the Patient Safety database.
Responsible for generating, sending, and tracking medically relevant queries for follow-up information that is required for an individual case safety report
Provide product advice as required, especially with regards to case reports that are Suspected Unexpected Serious Adverse reaction (SUSAR)
Ensure compliance with global and local procedural documents and implementation of client
and TCS, policies, procedures, and processes.
Location
Mumbai
Job Function
BUSINESS PROCESS SERVICES
Role
Executive
Job Id
380182
Desired Skills
Medical Knowledge
Desired Candidate Profile
Qualifications
: MBBS, MD
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