Associate Pharmacovigilance Project Manager – Europe

Job not on LinkedIn

🕒 July 21

🇪🇺 Europe – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

👷‍♀️ Project Manager

👻 Ghost score 24%

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

• Acting as the primary contact point for project-related matters • Managing client’s expectations to make sure the client is satisfied with services of PrimeVigilance, and that the work PrimeVigilance delivers meets, or even exceeds, the clients’ expectations. • Preparing project scope and objectives based on the signed agreement between the client and PrimeVigilance. • Project activities planning, including deadlines and interim milestones • Reporting for the client and the PrimeVigilance management, e.g., preparation of Monthly reports, serving as basis for invoicing.

🎯 Requirements

• Proven track record of demonstrated Pharmacovigilance activities including processing and quality review of ICSRs • Writing, or contributing to aggregate reports • Literature screening, reconciliation, and preparation of SOPs • PV Project Management experience from ideally a service provider / CRO • Health Care Professional or Life Science Graduate • Be comfortable with communicating at senior levels within pharmaceutical organizations • Have good leadership qualities including skills in planning, mentoring, meeting facilitation, communication and problem solving.

🏖️ Benefits

• Flexible working hours • Professional development opportunities