5 дней назад
Contract Negotiator (Clinical Research) - Portugal - Sponsor Dedicated
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Contract Negotiator (Clinical Research) - Portugal - Sponsor Dedicated (Clinical Research): Developing global contracting strategies, investigator grants, contract language, budgets, and site agreements for clinical trials with an accent on sponsor requirements, regulatory compliance, and financial accuracy. Focus on negotiating complex contract terms, coordinating study teams and stakeholders, and maintaining contracting performance across timelines and project plans.
Location: Lisbon, Portugal
Company
provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.
What you will do
- Develop global contracting strategies, investigator grants, estimates, proposal text, contract language, payment language, and budget templates.
- Manage contracting systems, tools, training materials, databases, tracking tools, timelines, and project plans for assigned sponsors and clinical studies.
- Collaborate with sponsors, study teams, stakeholders, and regional and country teams to deliver contracting activities within agreed project requirements.
- Provide legal, operational, and financial contracting support for site agreements, study initiation, and clinical trial maintenance.
- Collect, analyze, and communicate contracting intelligence, performance metrics, and out-of-scope activities.
- Support quality management, client presentations, colleague mentoring, and the development of long-term client relationships.
Requirements
- Based in Lisbon, Portugal.
- Bachelor's degree in a related field or an equivalent combination of education, training, and experience.
- At least 5 years of relevant sponsor or clinical research organization experience in clinical site contracting, including global or regional contract negotiation.
- Strong negotiation, communication, interpersonal, legal, financial, and technical writing skills.
- Knowledge of the regulated clinical trial environment, drug development, GCP/ICH, applicable regulations, SOPs, and corporate standards.
- Ability to work independently in a matrix environment, manage timelines and metrics, and lead, coach, and mentor colleagues.
Culture & Benefits
- Full-time employment within a global clinical research and healthcare intelligence organization.
- Collaboration with sponsors, study teams, and stakeholders across regional and country teams.
- Work focused on clinical trial development, regulatory compliance, and improved patient outcomes.
- Commitment to diversity, inclusion, belonging, and equal opportunity.
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