Pharmacovigilance Specialist (Medical/Clinical Safety)

Biomapas Group; Polska; À distance; PLN 120 000 - 180 000; Plein temps

Avantages offerts par ce poste

Remote work

Annual bonus

Health insurance

Accident & travel insurance

Vaccinations

International team

Team meetings

Résumé du poste

Biomapas Group is expanding its Pharmacovigilance team. We seek a Pharmacovigilance Specialist to ensure compliance with QoL standards and regulatory requirements across global safety information activities.

The role covers safety data processing, literature monitoring, and collaboration with cross-functional teams in a fully EU-based remote setup. The ideal candidate has a Life Science degree, 4+ years in pharmacovigilance, and proficiency with PV databases and MedDRA coding, plus fluency in

Qualifications

• University degree in 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.

Responsabilités

• Responsible for processing of IC SRS, 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
• Participate in Project / Study Team meetings as the Safety and Pharmacovigilance representative
• Oversee the planning, coordination, and quality review of aggregate safety reports, support the preparation and submission of regulatory safety documents (e.g., DSURs, 6MLL)
• Supervision of local handling, including preparation and submission, of Periodic Safety Update Reports, Risk Management Plans and risk minimization activities
• Collaborate with medical, safety physicians, and data management, IT, other functions to ensure timely and accurate reporting or reports delivery
• Act as Biomapas and/or contractual partners 24/7 local contact person or back up for pharmacovigilance at local level
• Ensure the survey and monitoring of national / regional pharmacovigilance regulations
• 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
• Support of continuous safety profile monitoring, detection of new signals and evaluation
• Participate in related inspection and/or audits, including post inspection/audit support, when required

Connaissances

Attention to detail

Time management

Problem solving

Fluent English

Project management

Formation

University degree in Life Science

Outils

Argus/ArisG PV databases

MedDRA coding

Description du poste

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

• Responsible for processing of IC SRS, 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
• Participate in Project / Study Team meetings as the Safety and Pharmacovigilance representative
• Oversee the planning, coordination, and quality review of aggregate safety reports, support the preparation and submission of regulatory safety documents (e.g., DSURs, 6MLL)
• Supervision of local handling, including preparation and submission, of Periodic Safety Update Reports, Risk Management Plans and risk minimization activities
• Collaborate with medical, safety physicians, and data management, IT, other functions to ensure timely and accurate reporting or reports delivery
• Act as Biomapas and/or contractual partners 24/7 local contact person or back up for pharmacovigilance at local level
• Ensure the survey and monitoring of national / regional pharmacovigilance regulations
• 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
• Support of continuous safety profile monitoring, detection of new signals and evaluation
• 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
• Influenza vaccines
• Rewarding referral policy
• Workplace establishment allowance (fully remote)
• Team building, global meetings, B active events