The Pharmacovigilance Specialist will be responsible for ensuring the operational delivery of assigned tasks at the project level, with a focus on safety case reporting, processing of safety case report data, and literature screening activities. The role involves communication with the Pharmacovigilance Team Leader and Pharmacovigilance Manager regarding potential risks related to operational delivery, quality standards, client relationships, and the company's reputation, as well as addressing ad hoc project tasks and requirements.CV must be in English language for further assessment.Position is full-time remote/home-based in any European country and Turkey.Responsibilities:Oversee and manage the workflow of safety case reports, ensuring efficient processingPerform triage on safety case reports to assess priority and necessary actionsReview, manage, and file source documentation in compliance with regulatory requirementsProcess safety case reports, including SDB data entry, narrative writing, seriousness assessment, medical review (including causality and expectedness assessments), and reporting requirements evaluationConduct follow-up activities and manage queries related to safety case reports Execute quality control checks on data entry and case processing to ensure accuracy and complianceReconcile safety case reports to ensure consistency and completeness of dataPrepare line listings to summarize and report on safety case dataRequirementsUniversity degree in Life Science fieldAt least 1 year of experience in Safety and Pharmacovigilance within the pharmaceutical or Contract Research Organization (CRO) industryExperience of clinical trial case processing in a safety database.Proficiency in both verbal and written local language and English Strong expertise with MS Office Beneficial experience with Veeva Vault Safety systemKnowledge of EU GVP modules and applicable global safety regulations (e.g. ICH, FDA reporting requirements)BenefitsFull remote flexible workProfessional growth and career opportunitiesInternational team and environment
The Pharmacovigilance Specialist will be responsible for ensuring the operational delivery of assigned tasks at the project level, with a focus on safety case reporting, processing of safety case report data, and literature screening activities. The role involves communication with the Pharmacovigilance Team Leader and Pharmacovigilance Manager regarding potential risks related to operational delivery, quality standards, client relationships, and the company's reputation, as well as addressing ad hoc project tasks and requirements.
CV must be in English language for further assessment.
Position is full-time remote/home-based in any European country and Turkey.
Responsibilities:
- Oversee and manage the workflow of safety case reports, ensuring efficient processing
- Perform triage on safety case reports to assess priority and necessary actions
- Review, manage, and file source documentation in compliance with regulatory requirements
- Process safety case reports, including SDB data entry, narrative writing, seriousness assessment, medical review (including causality and expectedness assessments), and reporting requirements evaluation
- Conduct follow-up activities and manage queries related to safety case reports
- Execute quality control checks on data entry and case processing to ensure accuracy and compliance
- Reconcile safety case reports to ensure consistency and completeness of data
- Prepare line listings to summarize and report on safety case data
Requirements
- University degree in Life Science field
- At least 1 year of experience in Safety and Pharmacovigilance within the pharmaceutical or Contract Research Organization (CRO) industry
- Experience of clinical trial case processing in a safety database.
- Proficiency in both verbal and written local language and English
- Strong expertise with MS Office
- Beneficial experience with Veeva Vault Safety system
- Knowledge of EU GVP modules and applicable global safety regulations (e.g. ICH, FDA reporting requirements)
Benefits
- Full remote flexible work
- Professional growth and career opportunities
- International team and environment
Biomapas is a functional and full outsourcing solution provider to the global life science industry.
As a trusted partner for biopharmaceutical, medical device, cosmetics, and food supplement companies, we have one-stop-shop clinical research capabilities in high recruiting countries, delivering regulatory and pharmacovigilance excellence across Europe, CIS, MENA, and LATAM regions through the entire product lifecycle.
Our in-house experience combined with a hands-on mindset allows for tailored solutions to complicated challenges that emerge on your path to commercialization. Our professionals execute your projects efficiently, cost-effectively and aspire to partner with you and become an integral part of your team from Early Development to Commercial success.
Biomapas is a functional and full outsourcing solution provider to the global life science industry.
As a trusted partner for biopharmaceutical, medical device, cosmetics, and food supplement companies, we have one-stop-shop clinical research capabilities in high recruiting countries, delivering regulatory and pharmacovigilance excellence across Europe, CIS, MENA, and LATAM regions through the entire product lifecycle.
Our in-house experience combined with a hands-on mindset allows for tailored solutions to complicated challenges that emerge on your path to commercialization. Our professionals execute your projects efficiently, cost-effectively and aspire to partner with you and become an integral part of your team from Early Development to Commercial success.
