Pharmacovigilance Specialist - Remote

1w1 week ago

Biomapas

PT · Full-time · €30,000 – €50,000

About this role

Join our global team as a Pharmacovigilance Specialist in Portugal on a remote, home-based basis. Assure compliance with local and regional Quality Management System. Exchange relevant safety and pharmacovigilance information while acting as Local Safety Officer and Medical Information Specialist.

Communicate with Health Authorities and ensure compliance with applicable local guidelines and regulations. Collect, process, and communicate safety information, product quality complaints, and medical device incidents. Maintain and establish quality standards for local pharmacovigilance activities.

Monitor local literature weekly and participate in inspections or audits. Survey and monitor national pharmacovigilance regulations. Handle medical information enquiries from patients and health care professionals in an international team environment.

Benefit from professional growth and career opportunities in a rewarding international setting. Enjoy bonuses based on annual performance, additional health insurance, and team building with global meetings. Thrive in a remote role with supportive policies like referral rewards.

Requirements

Biologist, Pharmacist, Medical Doctor, or other life science degree
2-year experience in Pharmacovigilance
Fluent in English and Portuguese languages
Computer literacy (MS Office), experience with PV databases
Strong organizational and time management skills
Ability to work independently and in a team

Responsibilities

Act as Local Safety Officer and Medical Information Specialist in Portugal (nomination as per local requirements)
Act as 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 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 inspections and/or audits