Full-Time Pharmacovigilance Medical Writer II
Ergomed is hiring a remote Full-Time Pharmacovigilance Medical Writer II. The career level for this job opening is Experienced and is accepting Lisbon, Portugal based applicants remotely. Read complete job description before applying.
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Ergomed
Job Title
Pharmacovigilance Medical Writer II
Posted
Career Level
Full-Time
Career Level
Experienced
Locations Accepted
Lisbon, Portugal
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Job Details
We are looking for a pharmacovigilance medical writer to join our team. The Medical Writer will be responsible for medical writing including:
- PSURs/PBRERs
- PADERs
- ACOs
- DSURs
- RMPs
QC and review of all written output from the operations team as required
Supporting the project managers to determine scheduling of the aggregate reports for which they are responsible
In conjunction with the Quality, Compliance and Training Manager identify areas for improvement and address via training, clarifying changes to SOPs/OGs/templates
Complete quality documentation of aggregate reports
Attending kick off meetings with new clients as required
Attending audits and inspections as required
Providing aggregate report training
MD, pharmacy or Life Science degree (Masters or PhD is desirable)
Strong previous experience in Pharmacovigilance (Aggregate report writing, case processing, signal detection or risk management) within ideally a CRO environment
Ability to manage multiple and varied tasks and prioritize workload with attention to detail
Ability to effectively train and mentor Associate Medical Writers
Must be a strong team player
Fluency in English, an additional language is a benefit
FAQs
What is the last date for applying to the job?
The deadline to apply for Full-Time Pharmacovigilance Medical Writer II at Ergomed is
17th of August 2025
. We consider jobs older than one month to have expired.
Which countries are accepted for this remote job?
This job accepts [
Lisbon, Portugal
] applicants. .
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