4 дня назад
Experienced Clinical Research Associate, Multi-Sponsor, France (Oncology)
Вакансия из Hirify Global, списка международных tech-компанийДля мэтча и отклика нужен Plus
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Experienced Clinical Research Associate, Multi-Sponsor, France (Oncology) (clinical monitoring/GCP): Conducting site selection, initiation, monitoring, and close-out visits for oncology studies across France with an accent on protocol compliance, regulatory requirements, and study documentation. Focus on tracking recruitment, CRF completion, data queries, TMF/ISF maintenance, and resolving site quality issues while travelling nationwide.
Location: France; hybrid or home-based in Paris, Lyon, or Marseille, with nationwide travel required
Company
Provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.
What you will do
- Conduct site selection, initiation, monitoring, and close-out visits according to study protocols, SOPs, GCP, ICH, and applicable regulations.
- Train assigned sites on study protocols and maintain regular communication to manage expectations and resolve issues.
- Track regulatory submissions, approvals, recruitment, enrollment, CRF completion, and data query resolution.
- Verify the quality and integrity of site practices and ensure TMF and ISF documentation is complete and compliant.
- Document monitoring findings and action plans through visit reports, follow-up letters, and other study records.
- Collaborate with study team members to support project execution and study start-up activities.
Requirements
- Bachelor’s degree in a scientific or healthcare discipline, or an equivalent combination of education, training, and experience.
- At least 2 years of clinical oncology experience is mandatory.
- Advanced knowledge of GCP, ICH guidelines, clinical research regulations, and protocol requirements.
- Proficiency with Microsoft Word, Excel, PowerPoint, laptops, and applicable mobile devices.
- Good written and verbal English communication skills, along with organizational, problem-solving, time-management, and financial-management skills.
- Ability to travel nationwide and work flexible hours in a hybrid or home-based arrangement in Paris, Lyon, or Marseille.
Culture & Benefits
- Full-time employment in a hybrid or home-based work arrangement.
- Work with experienced clinical staff and multidisciplinary study teams.
- Training in therapeutic areas, protocols, and clinical research procedures.
- Work focused on accelerating the development of medical treatments and improving patient outcomes.
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