Pharmacovigilance Manager

2+ years

Not Disclosed

Istanbul

10 Jan. 3, 2025

Job Description

Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Pharmacovigilance Manager
Location: Istanbul, Turkey
Date Posted: December 12, 2024

Join Teva Pharmaceuticals in shaping the future of global health as a Pharmacovigilance Manager. Be a part of a mission-driven organization that makes health more accessible and affordable while improving the lives of millions worldwide.

Responsibilities:

Safety Oversight: Monitor and evaluate the safety profile of Teva products to ensure compliance with global pharmacovigilance regulations.
Regulatory Submissions: Prepare and manage the documentation and submission of safety reports, including PSURs, CCSI, and RMPs.
Adverse Event Reporting: Collaborate across teams to facilitate timely adverse event submissions to regulatory authorities.
Process Management: Develop, implement, and maintain processes and SOPs that adhere to pharmacovigilance guidelines.
Stakeholder Liaison: Act as the primary contact for regulatory agencies and external partners concerning drug safety.
Risk Management: Contribute to risk management plans and other safety-related documentation.
Audit Participation: Support audits and inspections, ensuring compliance with all applicable standards.
Team Development: Train and mentor team members, fostering skill development and collaboration.
Cross-functional Collaboration: Participate in projects to improve drug safety processes and ensure process optimization.

Qualifications:

Education: Bachelor’s degree in life sciences, pharmacy, or a related discipline.
Experience:
- At least 2 years in pharmacovigilance, drug safety, or a related field within the pharmaceutical industry.
- Hands-on experience in safety data review and adverse event analysis.
Regulatory Knowledge: Proficient in local pharmacovigilance regulations and guidelines.
Skills:
- Strong communication and interpersonal abilities for cross-team collaboration.
- Analytical mindset with meticulous attention to detail.
- Proficiency in Microsoft Office Suite and familiarity with pharmacovigilance systems.

Why Join Teva?

Work with a global leader in generics and healthcare solutions.
Be part of an inclusive and diverse workplace.
Contribute to impactful projects that improve lives globally.

Application for Current Teva Employees:
If you’re currently working with Teva, apply through the Internal Career Site on "Employee Central" for priority consideration.

Equal Opportunity Commitment:
Teva Pharmaceuticals champions diversity and equal opportunity in employment. We provide accommodations to support candidates throughout the recruitment process and ensure an inclusive experience.

For more details, visit the Teva Careers page and make a meaningful difference in global health.

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Pharmacovigilance Manager

Job Description

Responsibilities:

Qualifications:

Why Join Teva?

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