Senior Director, ICSR

Job not on LinkedIn

🔥 22 minutes ago

🌐 New Zealand, Bulgaria – Remote

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⏰ Full Time

🟠 Senior

👔 Director

👻 Ghost score 17%

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Logo of ERGOMED

ERGOMED

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 for ongoing projects • Analyze workload, productivity and resource utilization and reallocate resources as needed • Manage Associate Directors and oversee employees to ensure effective utilization and productivity • Notify the Resourcing department and open requests for additional resources when required • Propose process changes within project teams to ICSR leadership • Introduce best practices to increase 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 scope 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 • 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 detail and multitasking • Excellent management skills, including delegation, time and issue management • Technical skills • Team working skills • Advanced literacy in MS Office • Experience in staff management • Experience in project budget reviews and resource allocation • Experience with Critical CAPAs and quality processes

🏖️ Benefits

• Remote work availability • Flexible work environment • Growth opportunities • Collaborative team environment • Training and mentoring opportunities • Supportive workplace culture • Diversity, belonging and inclusive environment

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