Descripción de la oferta
SOLTI is an academic research group that performs clinical trials of excellence in oncology. Currently, SOLTI is comprised of over 550 renowned research professionals distributed over a broad network of more than 100 leading hospitals in Spain, Portugal, France and Ireland.SOLTI focuses its efforts on developing cutting-edge clinical trials with novel targeted therapeutics including innovative translational research, fostering the participation in international networks and promoting excellence in the management of cancer among their members.About the roleWe are currently seeking a Senior Clinical Trial Assistant (Sr CTA) to take ownership of the operational coordination of assigned studies and contribute with increasing autonomy throughout the study lifecycle.Reporting to the Clinical Operations Development Manager (CODM), you will be part of the Clinical Operations team, playing a key role in ensuring the smooth execution of clinical trials. While you will collaborate with the Regulatory & CTA team when needed, your primary focus will be on clinical operations.Key ResponsibilitiesCoordinate the day-to-day operations of assigned studies, including TMF maintenance, logistics and milestone tracking.Maintain and organize the Trial Master File (TMF), ensuring documentation is accurate, complete and up to date.Monitor and update study milestones, enrollment data and site activity in the CTMS, proactively identifying delays or inconsistencies.Reconcile data across CTMS, eTMF and IRT systems, flagging discrepancies early.Support logistics related to central labs, IRT systems and study materials.Assist CRAs with site documentation and operational follow-up.Actively participate in study team meetings, contributing with a clear operational perspective.Collaborate on regulatory submissions (CTIS), EC/RA notifications and site contract management as required.Support the onboarding of junior CTAs and contribute to keeping operational SOPs updated.What You Bring3–5 years of experience as a CTA in clinical trials.Hands-on experience with eTMF, CTMS and CTIS.Solid knowledge of ICH-GCP and EU CTR.Ability to manage multiple studies simultaneously and effectively prioritize in a fast-paced environment.A proactive mindset with the ability to work independently and take initiative.Proficiency in written English; spoken English is a plus. Spanish required.What Will Set You ApartExperience in a CRO or other fast-paced clinical research environments.Proven ability to identify and improve operational processes.Strong collaboration skills and adaptability to evolving priorities.Experience mentoring or training colleagues.What We OfferJoin an organization committed to impactful, cutting-edge research:A role with autonomy to manage your studies and grow your operational expertise.Exposure to a diverse portfolio of studies, sponsors and investigators.Career development opportunities towards broader clinical roles.A collaborative team environment within a meaningful phase of transformation.In addition, we provide:Full-time position (38 hours/week) based in Barcelona.Hybrid work model: up to 3 days remote per week.Flexible working hours to support work-life balance.Meal voucher (Ticket Restaurant).Free English classes for professional development.Complimentary coffee and fresh fruit in the office.Additional benefits.If your background and experience align with the requirements of this position, we encourage you to apply and explore this exciting opportunity with us.SOLTI is an employer committed to Equal Opportunities regardless of sex, gender, sexual orientation, race, age, origin or disability.Get to know us at: www.gruposolti.org
