Pharmacovigilance Case Processing Specialist
1 week ago
The Opportunity
- To perform case processing and related activities in alignment with Global Data Management.
- Process cases in accordance with regulatory requirements and industry standards.
Responsibilities
- End-to-end case processing, including intake, triage, case processing, quality check, and submissions.
- Investigate and resolve E2B rejections with successful submissions.
- Support major health authorities’ audits and inspections as presenter to auditors.
- Clarify day-to-day case inquiries from various serious and non-serious cases.
- Participate in SOP reviews and provide changes in accordance with ICH and GVP guidelines.
- Assist with mentoring and training activities in case processing teams.
- Ensure quality data is analyzed for trending and take steps for Quality Improvement.
Your Experience and Qualifications
- M.Pharm/Pharm D/BDS post-graduation in registered life sciences.
- 5+ years of experience in pharmacovigilance case processing and related activities in alignment with Global Data Management.
Teva’s Equal Employment Opportunity Commitment
Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva’s global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin, or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.
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