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Cencora

Senior Specialist, Local Pharmacovigilance

RemoteGreece only
Published
Experience
Senior
Employment
Full-time
Salary not disclosed
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No BS summary

Senior Pharmacovigilance Specialist with 2+ years of experience in regulatory affairs or related fields. Must be fluent in English and the local language. Bachelor's degree in life sciences or equivalent required. Certification in regulatory affairs preferred.

Required languages

English business fluentGreek

What you'll do

  • Set up and manage the local pharmacovigilance system, including oversight of local PV activities.
  • Local Literature Search
  • Local ICSR Collection and Management
  • PV Intelligence Screening
  • Local PSMF Maintenance (where applicable)
  • Setting up Local Organized Data Collection
  • Local PVA Management
  • Local adaptation and submission of PSUR / RMP (where applicable)
  • Local signal detection (where applicable)
  • Implementation of additional Risk Minimization Measures
  • Reviewing materials relating to local post-authorization safety studies
  • Participate in PV-relevant audits and inspections
  • Attend regular meetings according to project meeting schedule
  • Provide monthly PV report on status of local PV system in the country/ies
  • Ensure PV training of affiliate employees, service providers and Third Parties
  • Close cooperation with the global PV system of the client as well as related global and local departments and functions
  • Issue, review and maintain pharmacovigilance procedures (i.e. Standard Operating Procedures, Working Practices) related to the local tasks in connection with client procedures
  • Close cooperation with the respective Deputy and providing the Deputy with information on relevant current PV activities
  • Identify and escalate any Medical Information requests to an appropriate team according to applicable timelines.
  • 24/7 availability with the Competent Authority in the country for pharmacovigilance-related matters.
  • Act as official liaison with the Competent Authority in the country for pharmacovigilance-related matters.
  • Maintain oversight of local PV system to ensure compliance with national laws and regulations.
  • Notify the health authority promptly of significant safety concerns, product recalls or changes in the benefit-risk profile of the products.
  • Coordinate the distribution of national safety communications, such as Direct Healthcare Professional Communications.
  • Ensure local pharmacovigilance system updates and validations.
  • Internally, serving as point of contact for the EU-QPPV and the global PV team.
  • Deputy is assuming responsibility in case of planned or unplanned absence .

What they require

  • Bachelor's degree in life sciences, pharmacy, chemistry, biomedical sciences, engineering, quality management, or a related field, or equivalent experience required.
  • 2+ years of experience in regulatory affairs, quality assurance, compliance, documentation control, or a related field required.
  • Certification in regulatory affairs, quality management, compliance, auditing preferred.

Benefits

  • Full time

Cencora is an innovative company focused on improving the lives of people and animals and creating healthier futures.

HealthcareEnterpriseamerisourcebergen.com/
Salary not disclosed