Medical Writer III, Pharmacovigilance

Job not on LinkedIn

🔥 0 minutes ago

🇵🇹 Portugal – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🏥📝 Medical Writer

👻 Ghost score 18%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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ERGOMED

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Founded 1997

💼 Consulting

🏥 Healthcare

📦 Logistics

Consulting • Healthcare • Logistics

ERGOMED is a global group providing specialized services to the biotechnology and pharmaceutical industries. It operates under different service lines, including Ergomed Clinical Research, PrimeVigilance, and ADAMAS Consulting, and is dedicated to providing full-service clinical research organization (CRO) capabilities. Focused on oncology, rare diseases, and complex trials, it also offers end-to-end pharmacovigilance and medical information services, as well as comprehensive GxP audits. Ergomed is committed to supporting drug development with a global presence in around 100 countries.

📋 Description

• Author, review, and quality check regulatory and pharmacovigilance documents, including PSURs/PBRERs, PADERs, ACOs, DSURs, and Risk Management Plans • Ensure documents are scientifically accurate, regulatory compliant, and delivered within agreed timelines • Collaborate with cross-functional teams to analyse, interpret, and present safety data • Act as a trusted point of contact for clients and support project delivery • Foster strong working relationships with clients • Provide guidance, mentoring, and knowledge sharing to junior medical writers • Support professional growth and development of Associate Medical Writers • Contribute to process improvements and enhancement of medical writing quality standards

🎯 Requirements

• MD, pharmacy, or Life Science degree • Minimum 2 years' experience in Medical Writing and associated fields (case processing, signal detection or risk management), ideally within 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 • Strong team-player skills • Fluency in English • Additional language is a benefit • Experience with regulatory and pharmacovigilance writing • Client-focused mindset and attention to detail

🏖️ Benefits

• Remote work option • Professional growth and development opportunities • Mentoring and knowledge-sharing opportunities • Collaborative and supportive work environment • Flexible work culture • Belonging and inclusive workplace culture • Opportunity to contribute to patient safety and global pharmaceutical work