Senior Director, ICSR

Job not on LinkedIn

🔥 0 minutes ago

🌐 New Zealand, Italy – Remote

🇳🇿 New Zealand – Remote 🇮🇹 Italy – 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 for ongoing projects and review target updates • Analyze workload, productivity and resource utilization and reallocate resources appropriately • Manage Associate Directors and oversee employees to ensure effective utilization and productivity • Notify the Resourcing department and open approved requests for additional resources • Propose changes to project team processes and introduce best practices • Train and mentor ICSR Line Managers and senior staff • Prepare analyses and reports • Review budgets and resource allocations for new projects and existing project scope • 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 • Review and address Quality department requests • Review and update operating procedures and guidelines • Participate in 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, clinical and ideally medical devices • Demonstrated leadership experience at a senior level • Excellent written and verbal communication skills • Excellent organization skills, including attention to details and multitasking • Excellent management skills, including delegation, time and issue management • Technical skills • Team working skills • Advanced literacy in MS Office • Experience in post marketing and clinical processing and staff management

🏖️ Benefits

• Remote work option • Collaborative and supportive team environment • Flexibility • Growth opportunities • Professional development through training and mentoring • Diverse and inclusive workplace • Opportunity to work on global pharmacovigilance and patient-safety initiatives