4 дня назад
Senior Clinical Research Associate (Clinical Trials)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Senior Clinical Research Associate (Clinical Trials): Supporting 2–3 clinical trials through site start-up, monitoring, data verification, investigational product management, safety reporting, and study close-out with an accent on GCP compliance and reliable clinical data. Focus on conducting on-site and remote monitoring, coordinating sites, training investigators, resolving data queries, and supervising junior CRAs.
Location: Remote position based in Spain, with Barcelona as the ideal location; regular travel to clinical trial sites is required.
Company
is a global full-service contract research organization providing clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies.
What you will do
- Support 2–3 clinical trials across study start-up, monitoring, data review, and close-out.
- Conduct site selection, evaluation, initiation, periodic monitoring, and termination visits both on-site and remotely.
- Train site staff, act as the main site contact, and ensure timely follow-up of trial activities and documentation.
- Perform source data verification, review CRFs and clinical data, and resolve data queries.
- Manage investigational products, trial materials, investigator files, safety reporting, and study documentation.
- Guide and supervise CRA I staff and support training, submissions, feasibility, and site budget activities.
Requirements
- University degree in a scientific, medical, or paramedical discipline.
- At least eight years of clinical research experience, including on-site monitoring as a CRA.
- Previous experience working for a CRO is required.
- Strong knowledge of clinical trial operations, GCP/ICH Guidelines, and applicable regulatory requirements.
- Fluent English and Spanish are required.
- Proficiency in Microsoft Office and willingness to travel.
Nice to have
- Experience across a broad range of therapeutic areas.
Culture & Benefits
- Full-time, permanent employment with a remote working arrangement based in Spain.
- Professional development supported through continuous training and close management.
- Collaborative one-team culture focused on quality and work-life balance.
- Opportunity to work with pharmaceutical, biotechnology, medical device, and consumer health clients.
- Inclusive and diverse work environment.
Hiring process
- Submit a CV and receive an acknowledgement of receipt.
- Qualified candidates are invited to a phone interview as the first step.
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