Senior Director of ICSR

Job not on LinkedIn

🔥 45 minutes ago

🌐 New Zealand, Portugal – Remote

🇳🇿 New Zealand – Remote 🇵🇹 Portugal – Remote

⏰ Full Time

🟠 Senior

👔 Director

👻 Ghost score 17%

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

• Manage the assigned ICSR Management Unit effectively • Ensure adequate resources within ICSR project teams to maximize productivity and utilization • Set productivity targets and review target updates • Analyze reports and reallocate resources within the ICSR Management Unit or across other units and departments • Manage Associate Directors and oversee employees to ensure effective utilization and productivity • Notify the Resourcing department and open approved requests for additional project resources • Propose changes to project team processes and introduce best practices to improve productivity and utilization • Train and mentor ICSR Line Managers and senior staff • Prepare analyses and reports • Review budgets and resource allocations for new projects and new scopes of work • Support Directors of Projects, Business/Commercial, Operations, and Project Analytics teams • Assist HR with recruitment, performance evaluation, promotion, retention, and termination activities • Review and approve Critical CAPAs from the ICSR Management Unit • Review and address Quality department requests • Review and update operating procedures and guidelines • Perform business development activities

🎯 Requirements

• Life science graduate, pharmacy, nursing, other healthcare-related qualification, or experience in pharmacovigilance • Extensive experience in pharmacovigilance case processing, including post-marketing and clinical experience; ideally medical devices • Demonstrated leadership experience at a senior level • Excellent written and verbal communication skills • Excellent organization skills, including attention to detail and multitasking • Excellent management and delegation skills • Time and issue management skills • Technical skills • Team-working skills • Advanced literacy in MS Office

🏖️ Benefits

• Remote work availability • Flexible work environment • Growth opportunities • Collaborative team environment • Training and mentoring • Global reach and purpose-driven work • Diverse and inclusive workplace • Supportive culture and belonging • Opportunity to work with experts in clinical research, pharmacovigilance, and quality consulting