5 дней назад
Senior Site Contract Associate - IQVIA Biotech
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Senior Site Contract Associate - IQVIA Biotech (Clinical Research/Contracting): Supporting start-up contracting activities for biotech clinical trials, including investigator grant estimates, contract negotiations, budgets, proposals, and study documentation with an accent on regulated clinical research and sponsor collaboration. Focus on interpreting pricing models, maintaining contracting systems and CTMS data, applying GCP/ICH requirements, and delivering contracting activities within project timelines and financial goals.
Location: Home-based in Bulgaria, Hungary, or Romania; Sofia, Bulgaria is also listed.
Company
Biotech supports biotech and emerging biopharma companies with clinical development services across phases and therapeutic areas.
What you will do
- Support start-up contracting activities for assigned sponsors, studies, and multi-protocol programs, including pre-award work.
- Prepare investigator grant estimates, proposal text, bid grids, budgets, and pricing model interpretations.
- Maintain contract and budget templates, contracting systems, CTMS data, tracking tools, timelines, and project plans.
- Collaborate with sponsors, stakeholders, and regional and country teams to deliver project scope.
- Provide operational and financial contracting support for clinical trial initiation and maintenance.
- Monitor contracting efficiency, timelines, financial goals, performance metrics, and quality standards.
Requirements
- Bachelor’s degree in life sciences or healthcare.
- More than 6 years of relevant experience, including demonstrable contract negotiation experience.
- Experience in clinical site contracting within a sponsor or clinical research organization.
- Knowledge of regulated clinical trial environments, drug development, GCP/ICH, applicable regulations, SOPs, and corporate standards.
- Strong negotiation, communication, technical writing, organization, planning, and interpersonal skills.
- Strong knowledge of Microsoft Office and email applications, plus the ability to manage clinical trial contracts and budgets.
Culture & Benefits
- Home-based work arrangement for candidates in Bulgaria, Hungary, or Romania.
- Collaboration with biotech and emerging biopharma sponsors across clinical development programs.
- Agile structure and collaborative working environment.
- Work focused on accelerating innovative medical treatments and improving patient outcomes.
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