Team Manager - Medical Safety /pv/Aggregate Report Writting

Neptune Consultants
  • Hyderabad, Mumbai, Pune
  • Confidential
  • 4-9 years
  • 13 May 2015

  • Medical Services

  • Hospitals/ Health Care, Pharmaceuticals/ Life Sciences/ Clinical Research
Job Description

Job Description :

Prepares medical input to aggregate, clinical and safety regulatory reports
Provides expert evaluation on the clinical context of adverse event reports, assessment on the medical conditions, and the implications on Company drugs.
Provides Pharmacovigilance input into updates of the Company Core Data Sheet.
Leads cross-functional teams, such as safety management teams and operational work groups [Research, Drug Regulatory Affairs, Medical Affairs, Medical Information, Statistics, Safety Data Management, Epidemiology and other related departments]
Assist the BSL/PVL in monitoring the safety profile of products potentially including activities such as literature review, evaluation of individual cases or signal detection
Performs medical assessment and related activities for single cases, including collecting additional follow-up information as necessary, medical evaluation of quality defects, review of line listings of single cases, literature review and preparation of investigator notifications and periodic medical assessments for ethics committees.
Together with the BSL/PVL, co-author the PSUR including analytical input to PSUR for known and potential risks defined in the RMP.
With BSL/PVL, assist in the development, maintenance and implementation of the RMP including the coordination with other line functions for associated activities such as updates, management of large datasets for analysis purposes and the ongoing tracking of commitments and effectiveness measures
Assist in evaluating and writing other safety deliverables including but not limited to clinical overviews, ad hoc health authority queries, drug safety product profile (DSPP), drug safety update report (DSUR)
Assist in providing safety input to DRA and clinical documents (e.g. core data sheet and investigator brochure)
Play an active role in standing and ad hoc Safety Management Team (SMT) and Safety Project Team (SPT) meetings
Play an active role in SIGDET and MSRB meetings including preparatory activities
Interface with the clinical team for safety matters including follow-up on events of interest and input into site queries regarding adverse events, updating on PVO requirements
Lead the training and mentoring of internal and cross-functional team members

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