Clinical Research Coordinator

1 semana atrás


Ituiutaba, Brasil Planet Pharma Tempo inteiro

Job Title: Site Support Colleague (Contract) Location: São Paulo, Brazil (Onsite) Contract Length: 6 months Workload: 0.5 FTE (part-time, approx. 2–3 days per week)About the RoleWe are working with a global leader in the life sciences sector to recruit a Site Support Colleague for their São Paulo operations. This part-time, 6-month contract is an excellent opportunity to gain experience in a highly regulated, clinical environment.The role will provide hands-on support at a local research and development site, ensuring that clinical and operational teams have the tools, systems, and environment needed to deliver high-quality, compliant outcomes.Key ResponsibilitiesAct as a first point of contact for on-site staff, ensuring smooth day-to-day functioning of clinical systems and processes.Support site activities related to ongoing research and trials, addressing operational issues promptly to minimise disruption.Maintain accurate records of support activities to align with Good Clinical Practice (GCP) and internal quality standards.Collaborate closely with site management, clinical operations, and IT to ensure seamless communication and issue resolution.Assist in monitoring compliance with site policies, SOPs, and regulatory requirements.Escalate complex technical or procedural issues to senior colleagues or global support teams when required.What We're Looking For1–3 years' experience in a clinical research, site support, or related operational role.CTA or Clinical Trial Coordinator background would be highly suitable for this position.Understanding of working within GCP-regulated environments is strongly preferred.Strong problem-solving and troubleshooting skills with attention to detail.Excellent communication skills and a collaborative approach when working with multidisciplinary teams.Ability to work part-time on-site in São Paulo (approx. 2–3 days per week).Why Join?Contribute to meaningful clinical research supporting global health.Gain valuable experience in a regulated, pharmaceutical environment.Flexible part-time role with exposure to cross-functional teams.



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