Pharmacovigilance Specialist is responsible for assuring compliance with local and regional Quality Management System and exchange relevant safety and pharmacovigilance information.
All CVs must be submitted in the English language for consideration.
Responsibilities- Act as a Local Safety Officer and Medical Information Specialist in Portugal (nomination as per local requirements)
- Act as a Local Safety Officer and Medical Information Specialist in UK and provide support for UK projects (nomination as per local requirements)
- Communicate with Health Authorities
- Ensure compliance with applicable local guidelines and regulations
- Collect, process, and communicate of safety information, product quality complaints and medical device incidents
- Maintain and establish quality standards for local pharmacovigilance activities
- Ensure weekly monitoring of local literature review
- Participate in inspection and/or audits
- Ensure the survey and monitoring of national pharmacovigilance regulations
- Receive and handle medical information enquiries from patients and health care professionals
Requirements
- Biologist, Pharmacist, Medical Doctor, or other life science degree
- 2-year experience in Pharmacovigilance
- Fluent in English and Portugal languages
- Computer literacy (MS Office), experience with PV databases
- Strong organizational and time management skills
- Ability to work independently and in a team
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
- Team building, global meetings
Top Skills
What We Do
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.
We keep our promises. Always.
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