Se busca un Gerente de Ensayos Clínicos para ICON, una organización global de investigación clínica. El rol implica la gestión de operaciones de ensayos clínicos, asegurando el cumplimiento de plazos, presupuesto y estándares de calidad, y la colaboración con equipos multifuncionales. Se requiere experiencia previa en gestión de ensayos clínicos, preferentemente en oncología, y un nivel avanzado de inglés. El puesto es presencial en Buenos Aires, con asistencia a la oficina una vez por semana.
Si buscás crecer en investigación clínica y tenés experiencia en gestión de ensayos, este puesto en ICON es para vos. Podrás gestionar operaciones y colaborar con equipos globales en un modelo híbrido en Buenos Aires.
Regional Senior Clinical Trial Manager ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers. As a Clinical Trial Manager at ICON, you will manage clinical trial operations activities, supporting your team and stakeholders to deliver high-quality outcomes across our clinical programmes. What You Will Do: You will manage day-to-day clinical trial management activities, supporting your team to deliver quality outcomes. Key responsibilities include: Plan and manage all aspects of clinical trials, ensuring adherence to timelines, budget, and quality standards. Collaborate with cross-functional teams to establish and implement clinical trial protocols and procedures. Build and manage strong relationships with trial investigators and stakeholders. Ensure all trials are conducted in compliance with local, national, and international regulations and ethical guidelines. Problem-solve and make critical decisions regarding trial design, vendor selection, and risk management. Your Profile: You will have solid clinical trial management experience, with the ability to manage competing priorities and develop your team. Required qualifications and experience: University degree in Medicine, Life Sciences, or an equivalent combination of education and experience. Demonstrated ability to drive clinical deliverables within a study. Previous experience in Oncology studies is a plus. Prior monitoring experience is preferred. Based in Buenos Aires. Open to attending the office once per week. Advanced level of English. Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. Benefits may include: Competitive base salary and performance related incentives Health and wellbeing programmes including medical, dental, and vision coverage where applicable Retirement and pension plans Life assurance and disability coverage Employee assistance programmes and wellbeing resources Learning and development opportunities through structured training and career pathways Benefits may vary depending on role and location. Visit our careers site to read more about the benefits ICON offers. Inclusion and Accessibility ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported. If you require reasonable accommodations during the recruitment process, please let us know or submit a request here . Are you a current ICON Employee? Please click here to apply