Pharmacovigilance Specialist (Medical/Clinical Safety)
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Before you apply
LocationGreece
Work moderemote
Typefull-time
SeniorityMid
Experience4+ yrs
DepartmentPharmacovigilance
Company size51–200 people
PostedOct 16, 2026 · 3w ago
Verified live3d ago
At a glanceSummarised by Seekless from the posting.
University degree in the Life Science field
At least 4+ years' experience in Pharmacovigilance, clinical safety and clinical development and expert knowledge of pharmacovigilance legislation
Knowledge of international regulations (ICH, EU GVP Modules, FDA)
Experience working with PV databases (e.g., Argus, ArisG) and MedDRA coding
Ability to interpret and apply global drug safety regulations
Fluent English and local country language
Eager to adopt automations and new technologies in daily tasks
Attention to detail, time-management and problem-solving skills
Project management experience is beneficial
Skills
Argus
ArisG
MedDRA
Benefits
Professional growth
Bonus
Health insurance
Remote work
Referral bonus
About the role
Join our global Pharmacovigilance team as a Pharmacovigilance Specialist (Medical/Clinical Safety).
Pharmacovigilance Specialist (Medical/Clinical Safety) is responsible for assuring compliance with the Quality Management System. Participating in the collection, safety review, processing and reporting of safety information in compliance with applicable global and local regulations and Biomapas standard operating procedures and guidelines.
Position is in any EU country.
Responsibilities:
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Responsible for processing of ICSRs, Serious Adverse Event (SAE) from Clinical trials (safety database entry, tracking, narrative writing, requesting follow-up from site, quality checks/review and reporting to client (s) or agencies for assigned projects)
•
Perform reconciliation of safety data
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Participate in Project / Study Team meetings as the Safety and Pharmacovigilance representative
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Oversee the planning, coordination, and quality review of aggregate safety reports, support the preparation and submission of regulatory safety documents (e.g., DSURs, 6MLL).
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Supervision of local handling, including preparation and submission, of Periodic Safety Update Reports, Risk Management Plans and risk minimization activities
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Collaborate with medical, safety physicians, and data management, IT, other functions to ensure timely and accurate reporting or reports delivery
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Act as Biomapas and/or contractual partners 24/7 local contact person or back up for pharmacovigilance at local level
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Ensure the survey and monitoring of national / regional pharmacovigilance regulations
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Collection and processing of any medical enquiry/inquiry/answer received via phone/e-mail/fax or by other means from any source
•
Support of weekly monitoring of local or global literature review
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Support of continuous safety profile monitoring, detection of new signals and evaluation
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Participate in related inspection and/or audits, including post inspection/audit support, when required
Requirements
•
University degree in the Life Science field
•
At least 4±years’ experience in Pharmacovigilance, clinical safety and clinical development and expert knowledge of pharmacovigilance legislation
•
Knowledge of international regulations (ICH, EU GVP Modules, FDA)
•
Experience working with PV databases (e.g., Argus, ArisG) and MedDRA coding
•
Ability to interpret and apply global drug safety regulations
•
Fluent English and local country language
•
Eager to adopt automations and new technologies in daily tasks
•
Attention to detail, time-management and problem-solving skills
•
Project management experience is beneficial
Benefits
•
Professional growth and career opportunities
•
International team and environment
•
Bonus based on annual performance
•
Personal accident and business trip insurance
•
Additional health insurance
•
Remote/home based
•
Rewarding referral policy
•
Workplace establishment allowance (fully remote)
•
Team building, global meetings