Want to know how your job could evolve with AI? Join the discussion and get your personalised AI career outlook. Click here.
C

Pharmacovigilance Officer

New
Language Requirement: English Work Type: Full Time Working Hours: 8 to 5 Applicant Location: Kenya

Job descriptions & requirements

Drug Safety (core PV oversight)

  • Establish and maintain a single-point system for collecting/collating all suspected adverse reaction reports (including from medical reps and CRAs)
  • Collect, evaluate, process, and submit Individual Case Safety Reports (ICSRs)
  • Prepare and submit Periodic Safety Update Reports (PSURs) as needed
  • Manage Risk Management Plans (RMPs)
  • Negotiate, implement, and maintain Safety Data Exchange Agreements (SDEAs)
  • Implement and maintain the Drug Safety System Database and Master Files, including data reconciliation (including with 3rd parties)
  • Conduct required literature searches
  • Respond to Health Authority safety queries on Company products
  • Contribute to Annual Product Quality Reviews (APQRs)
  • Train Company employees on drug safety procedures
  • Ensure compliance with jurisdiction-specific drug safety legislation
  • Ensure consistency of drug safety processes/procedures and staff training

External Stakeholder Relationship Management

  • Build and manage relationships with business partners, complying with PVA/SDEA requirements
  • Build relationships with Cipla Global and align with Global Drug Safety
  • Maintain a strong profile with regulatory authorities and industry bodies to positively influence company perception

Cross-Functional Alignment

  • Determine how the function can best serve the business
  • Measure stakeholder satisfaction/performance and identify improvements
  • Ensure adherence to SLAs and performance criteria

People Management

  • Hire appropriately skilled personnel in line with transformation objectives; maintain competence records and organograms
  • Provide and assess training for the DS team
  • Ensure PV induction training for new SSA employees
  • Keep DS team Job Descriptions current (annual review or on scope change)
  • Set SMART objectives for DNA (performance) purposes
  • Support ongoing training and career development
  • Manage DS team performance (with VP: Head of Quality)
  • Ensure HR policy adherence within the team


Drug Safety (core PV oversight)

  • Establish and maintain a single-point system for collecting/collating all suspected adverse reaction reports (including from medical reps and CRAs)
  • Collect, evaluate, process, and submit Individual Case Safety Reports (ICSRs)
  • Prepare and submit Periodic Safety Update Reports (PSURs) as needed
  • Manage Risk Management Plans (RMPs)
  • Negotiate, implement, and maintain Safety Data Exchange Agreements (SDEAs)
  • Implement and maintain the Drug Safety System Database and Master Files, including data reconciliation (including with 3rd parties)
  • Conduct required literature searches
  • Respond to Health Authority safety queries on Company products
  • Contribute to Annual Product Quality Reviews (APQRs)
  • Train Company employees on drug safety procedures
  • Ensure compliance with jurisdiction-specific drug safety legislation
  • Ensure consistency of drug safety processes/procedures and staff training

External Stakeholder Relationship Management

  • Build and manage relationships with business partners, complying with PVA/SDEA requirements
  • Build relationships with Cipla Global and align with Global Drug Safety
  • Maintain a strong profile with regulatory authorities and industry bodies to positively influence company perception

Cross-Functional Alignment

  • Determine how the function can best serve the business
  • Measure stakeholder satisfaction/performance and identify improvements
  • Ensure adherence to SLAs and performance criteria

People Management

  • Hire appropriately skilled personnel in line with transformation objectives; maintain competence records and organograms
  • Provide and assess training for the DS team
  • Ensure PV induction training for new SSA employees
  • Keep DS team Job Descriptions current (annual review or on scope change)
  • Set SMART objectives for DNA (performance) purposes
  • Support ongoing training and career development
  • Manage DS team performance (with VP: Head of Quality)
  • Ensure HR policy adherence within the team


Important safety tips

  • Do not make any payment without confirming with the BrighterMonday Customer Support Team.
  • If you think this advert is not genuine, please report it via the Report Job link below.

This action will pause all job alerts. Are you sure?

Cancel Proceed

Similar jobs

Lorem ipsum

Lorem ipsum dolor (Location) Lorem ipsum Confidential
4 years ago

Stay Updated

Join our newsletter and get the latest job listings and career insights delivered straight to your inbox.

v2.homepage.newsletter_signup.choose_type

We care about the protection of your data. Read our

We care about the protection of your data. Read our  privacy policy .

Or your alerts