Join our global Pharmacovigilance team as a Pharmacovigilance Associate.
Pharmacovigilance Associate is responsible for assuring compliance with local and regional Quality Management System and interact, exchange relevant safety and pharmacovigilance information.
Position is remote, home-based in EU.
All CVs must be submitted in the English language for consideration.
Responsibilities:
UAB "Biomapas" (“Biomapas”) processes personal data of job applicants for the purpose of selecting job candidates. More information about the processing of personal data is available online at https://www.biomapas.com/privacy-policy/.
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Join our dynamic global Pharmacovigilance team at Biomapas as a Pharmacovigilance Associate, where your expertise will play an essential role in assuring compliance with local and regional Quality Management Systems. This remote, home-based position is ideal for a dedicated professional like you, looking to make an impact while enjoying the flexibility of a fully digital workspace. As a Pharmacovigilance Associate, you'll engage with local literature to review and collect safety information, assisting local teams in effectively executing contracted pharmacovigilance activities. With your educational background as a Biologist, Pharmacist, Medical Doctor, or a related life science degree, you bring at least one year of experience in this field, making you an excellent fit for us. Fluency in English and native proficiency in German are crucial, as is your computer literacy with tools like MS Office and pharmacovigilance databases. You’ll excel with your strong organizational and time management skills, thriving both independently and within a collaborative team environment. Besides a competitive salary, we offer professional growth opportunities, an annual performance bonus, personal and business trip insurance, additional health coverage, and even the potential for a workcation. Join us, and let's create safer healthcare solutions together!
Biomapas is a functional and full outsourcing solution provider to the global life science industry, with key expertise in Clinical Trials, Regulatory Affairs and Pharmacovigilance. The company has significant presence across the CEE, Nordic and C...
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