7 дней назад
Senior Manager, Global Site Activation, Legal Liaison
201 500 - 374 100PLN
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Senior Manager, Global Site Activation, Legal Liaison (Clinical Research and Site Contracting): Providing operational support and guidance for clinical trial contracting, with an accent on contract templates, legal alignment, and country-specific requirements. Focus on resolving complex contracting issues, standardizing site contracting practices, and applying GCP/ICH and regulatory guidelines across EU clinical research activities.
Location: Warsaw, Poland
Annual base pay: PLN 201,500–374,100
Company
provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.
What you will do
- Provide study-specific contracting support to Project Managers, SSUMs, Site Contract Negotiators, and Global Template Developers.
- Serve as the primary operational contact for complex contracting issues and escalate legal matters to the Legal Department when appropriate.
- Advise stakeholders on approved contracting positions, templates, and contracting policies.
- Own and maintain the Global Site Contracts Library, including country-specific templates, guidance documents, and supporting materials.
- Lead contract template development, validation, maintenance, translation coordination, version control, and continuous improvement.
- Train and support Site Contracts teams while driving standardization, compliance, and operational excellence.
Requirements
- Master’s degree in law and demonstrable experience as a qualified lawyer.
- At least 5 years of relevant sponsor or clinical research organization experience in clinical site contracting.
- Demonstrable experience acting as an EU legal contract expert.
- Strong negotiation, communication, coordination, and collaboration skills, including the ability to challenge stakeholders.
- Excellent legal, financial, and/or technical writing skills.
- Thorough understanding of regulated clinical trials, drug development, GCP/ICH, and applicable regulatory guidelines.
Nice to have
- Experience in a pharmaceutical or CRO environment.
Culture & Benefits
- Full-time employment.
- Potential incentive plans, bonuses, health and welfare benefits, and other benefits may be offered depending on the position.
- Work within a global clinical research and healthcare intelligence organization.
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