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Sr Pv Manager

7+ years
Not Disclosed
10 April 30, 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

Sr PV Manager
Location: Finland
Category: Pharmacy & Clinical
Type: Full Time
Posted Date: February 28th, 2025
Job ID: R253662

About Cencora:
At Cencora, our people drive everything we do. We are united by our mission to create healthier futures, and each team member plays a vital role in fulfilling that purpose. If you're ready to make a global impact and be part of an innovative and caring organization, join us and shape the future of health.


Position: Sr PV Manager
Location: Pharmalex, Finland

Key Responsibilities:

Pharmacovigilance System Management:

  • Establish and maintain the local pharmacovigilance (PV) system.

  • Ensure all affiliate employees, service providers, and third parties are trained on PV requirements.

  • Provide pharmaceutical expertise across all PV functions.

Case Management & Oversight:

  • Oversee the full ICSR (Individual Case Safety Report) process—from intake to regulatory reporting.

  • Provide guidance across related services such as signal detection, compliance, and aggregate reporting.

  • Supervise team PV activities including literature screening, follow-ups, reconciliations, and complaint handling.

Regulatory & Client Communication:

  • Liaise with regulatory authorities and clients on all PV-related matters.

  • Review and approve essential safety documentation including PSURs, PADERs, DSURs, RMPs, and signal detection reports.

Documentation & Training:

  • Draft and review SOPs, working instructions, templates, and related procedural documents for PV projects.

  • Organize and deliver training sessions on PV procedural documents.

Audits & Compliance:

  • Prepare for and participate in internal and external PV audits and inspections.

  • Review and approve CAPAs to ensure compliance and continuous improvement.


Qualifications & Experience:

  • Several years of hands-on pharmacovigilance experience with in-depth understanding of PV principles.

  • Expertise in current pharmacovigilance regulations, both legislative and non-legislative.

  • Proven experience leading and mentoring PV teams.

  • Strong project management abilities, including equitable workload distribution and goal alignment.

  • Experience managing client relationships at departmental leadership level.

Skills Required:

  • Strong written and verbal communication skills with ability to convey critical issues and solutions across divisions.

  • Effective presentation skills.

  • Business fluency in English and Finnish.


What Cencora Offers:
Benefits vary by country and comply with local market standards. Eligibility and activation of specific benefits may differ for unionized positions.

Affiliated Company: PharmaLex

Equal Employment Opportunity:
Cencora is an equal opportunity employer and prohibits discrimination in all employment practices. We are committed to accommodating individuals with disabilities in accordance with applicable laws. For accommodation requests, contact 888.692.2272 or email
hrsc@cencora.com.


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