Local Contact Person – Pharmacovigilance, Regulatory Affairs

Job not on LinkedIn

🔥 0 minutes ago

🇸🇮 Slovenia – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🚔 Compliance

👻 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

• Act as Local Country Person Responsible for Pharmacovigilance and Regulatory Affairs (LCPPV/LCPRA) • Serve as the primary local Regulatory Affairs and Pharmacovigilance representative for Australia • Ensure compliance with national pharmacovigilance and regulatory requirements • Execute local pharmacovigilance and regulatory affairs activities • Support the Marketing Authorisation Holder in maintaining product compliance throughout its lifecycle • Communicate promptly and effectively with the Marketing Authorisation Holder and local regulatory authorities • Serve as the primary contact for local regulatory authorities on Regulatory Affairs and Pharmacovigilance matters • Screen local regulatory intelligence and provide expert advice for responsible regions • Collect and report locally suspected adverse drug reactions and individual case safety reports, including follow-ups and translations • Manage or oversee risk-minimization measures related to urgent safety restrictions and emerging safety issues • Support development and implementation of the local pharmacovigilance system in compliance with the global system and local regulations • Perform local non-indexed literature screening and regulatory-authority website screening for potential adverse drug reactions and safety information • Maintain accurate local records and documentation • Support the Regulatory Affairs and Pharmacovigilance Global Operations team • Prepare and collect documentation for regulatory-authority submissions • Review and provide linguistic input on local Product Information and mock-ups • Ensure compliance with Marketing Authorisation Holder and PrimeVigilance procedures • Support audits and inspections • Handle local quality-assurance tasks, including suspected falsified products, health-authority quality alerts and other local-market quality requirements

🎯 Requirements

• Bachelor's Degree in Life Sciences or Chemistry, Nursing or equivalent professional experience • At least 3 years of pharmacovigilance or safety-related experience in pharmaceutical, CRO, or regulatory environment • Good understanding of ICH GVP and local pharmacovigilance requirements through training or practical exposure • Experience in case handling, literature screening, or local PV activities is preferred • Prior experience in Regulatory Affairs is preferred but not mandatory • Proficiency in English • Additional language knowledge is advantageous • Strong skills in Microsoft Office applications, including Word, Excel, and PowerPoint • Ability to act as Local Country Person Responsible for Pharmacovigilance and Regulatory Affairs • Knowledge of national pharmacovigilance and regulatory requirements in Australia • Ability to support audits and inspections • Ability to handle local QA tasks, including suspected falsified products and health-authority quality alerts

🏖️ Benefits

• Remote work option • Permanent or contractor employment arrangement • Collaborative and supportive team environment • Flexibility, growth and belonging culture • Opportunity to work with global teams across Europe, North America, South America, Asia and Australia • Professional growth opportunities • Purpose-driven work helping protect patients • Exposure to clinical research, pharmacovigilance and quality consulting experts