Senior Pharmacovigilance Officer, Team Lead – Medical Device Experience

🕒 August 6

🇪🇸 Spain – Remote

⏰ Full Time

🟠 Senior

✨ Medical Officer

👻 Ghost score 16%

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

• Lead the team responsible for ICSR management for selected projects or groups of projects • Line manage ICSR staff • Ensure adequate task distribution and oversee workflow processes • Drive effective cooperation with clients in ICSR Management • Support achievement of company goals and objectives • Provide support to project team activities on behalf of the client and company • Create and maintain project-specific KPIs for contracted ICSR activities • Optimize procedures, trainings, and other actions to increase ICSR team efficiency • Propose process changes to the ICSR Operational Lead • Manage ICSR deviations with support from the ICSR Operational Lead • Review trackers and timesheet data and ensure accuracy • Participate in ICSR processing and second quality control of cases • Support other departments as instructed by the ICSR Operational Lead • Act as the assigned team subject matter expert • Support the RA & PV Network Department, including acting as LCPPV for the specified country and PRLS for the designated language when agreed with the line manager

🎯 Requirements

• Life science graduate, pharmacy, nursing, other healthcare-related qualification, or experience in pharmacovigilance • Strong previous work experience in pharmacovigilance • Minimum 1 year of work experience in a line manager role • Medical Device experience required • Excellent written and verbal communication skills • Organization skills, including attention to detail and multitasking • Delegation skills • Planning and time management skills • Technical skills • Team working skills • Fluent English, spoken and written • Advanced literacy in MS Office

🏖️ Benefits

• Remote work • Flexible work environment • Growth opportunities • Supportive and collaborative team culture • Professional development through work with experts in clinical research, pharmacovigilance, and quality consulting • Opportunity to contribute to patient safety and help bring safe and effective pharmaceutical treatment to patients around the world