Join Our Team as a Pharmacovigilance Data Associate in
Introductory Paragraph:
Our client is seeking an experienced and highly-motivated individual to join their team as a Pharmacovigilance (PV) Data Associate. As the PV industry continues to grow at an unprecedented pace globally, our client recognises that data management of adverse events plays a critical role in patient safety monitoring.
Key Responsibilities:
- Utilise CAPA systems for case processing
- Assure compliance with Good Pharmacovigilance practices
- Conduct quality checks on processed cases before submission
- Liaise with stakeholders such as medical information personnel
Qualifications & Skills Required:
-Relevant experience within pharmacovigilance or related field.
-Familiarity with international regulatory requirements relating to drug safety reporting.
-Sound understanding of database principles and electronic document management processes including proficiency using MedDRA coding software.
-Detail-oriented approach ensuring high levels of accuracy are attained when working under pressure while maintaining strict deadlines.
About The Company:
Our Client operates across Europe providing pharmaceutical companies innovative solutions designed specifically support clinical development programs from phase I through post-marketing activities by supplying expert consulting services coupled together rigorous attention detail throughout all phases life cycle product development process.
If you're passionate about promoting public health awareness initiatives whilst having drive succeed constantly evolving environment then we would love hear more!
