6 дней назад
Project Director (Oncology)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Project Director (Oncology/Clinical Trials): Overseeing global and complex oncology clinical trials or portfolios, including client liaison, project planning, budgets, quality management, and cross-functional execution with an accent on strategic planning, risk mitigation, financial control, and ICH-GCP compliance. Focus on leading project managers and study teams, managing trial performance and profitability, resolving protocol and quality issues, and supporting bid defense and continuous process improvement.
Location: Fully remote from the United Kingdom, Spain, Poland, Hungary, Romania, Serbia or Slovakia. International and domestic travel, including overnight stays, may be required.
Company
is a people-focused contract research organization combining clinical trial design, operational and medical expertise, biomarker and data analytics solutions, and oncology and rare-disease research.
What you will do
- Serve as the primary client liaison and support proposals, client presentations, and bid defense activities.
- Oversee complex oncology clinical trials or portfolios from establishment and planning through execution and closeout.
- Direct project managers and cross-functional study teams, setting expectations and driving delivery against project goals.
- Manage study budgets, profitability, billable hours, forecasting, scope changes, and change orders.
- Develop project plans, timelines, risk mitigation strategies, quality processes, metrics, and status reporting.
- Lead meetings, resolve study and protocol issues, ensure training compliance, mentor project managers, and support continuous improvement.
Requirements
- Degree or equivalent education and experience in a science or health-related field; an advanced degree is preferred.
- At least 8 years of clinical research experience and at least 5 years of direct project management experience.
- Experience managing highly complex global studies or portfolios, preferably in pharmaceutical and/or device research.
- Proficiency with Microsoft Office, Microsoft Project, eTMF, EDC, CTMS, and project management software.
- Mastery of ICH-GCP, project planning, risk management, change management, cross-functional leadership, and quality management.
- Excellent communication, presentation, negotiation, analytical, organizational, and interpersonal skills.
Culture & Benefits
- Fully remote work from specified European countries.
- Supportive and collaborative environment focused on work-life balance.
- Opportunities for team development, mentoring, and contribution to company SOPs.
- Work on clinical research supporting innovative cancer therapies and precision medicine.
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