
51 - 200 employees
Founded 1993
🚗 Transport
🤝 B2B
Transport • B2B
SYNVIA is a logistics and transport company specializing in secure, compliant, and customized supply chain solutions for high‑value and sensitive industries. The company provides multimodal transport (road, air, maritime), temperature‑controlled and regulated warehousing (including ICPE), handling of dangerous goods, customs transit services, and value‑added operations like co‑packing, labeling and kitting. SYNVIA focuses on B2B clients in sectors such as chemistry, energy, agriculture, cosmetics and public hygiene, emphasizing traceability, regulatory compliance, and operational agility.
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🗣️🇧🇷🇵🇹 Portuguese Required
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51 - 200 employees
Founded 1993
🚗 Transport
🤝 B2B
Transport • B2B
SYNVIA is a logistics and transport company specializing in secure, compliant, and customized supply chain solutions for high‑value and sensitive industries. The company provides multimodal transport (road, air, maritime), temperature‑controlled and regulated warehousing (including ICPE), handling of dangerous goods, customs transit services, and value‑added operations like co‑packing, labeling and kitting. SYNVIA focuses on B2B clients in sectors such as chemistry, energy, agriculture, cosmetics and public hygiene, emphasizing traceability, regulatory compliance, and operational agility.
• Conduct training relevant to your role and keep training records up to date; • Assist with administrative aspects of clinical trials, providing support to the study team (CRAs/monitors and clinical project managers); • Assist in collecting and preparing documents from investigative sites during the conduct of the clinical trial; • Prepare the study's Trial Master File (TMF) and assist in its ongoing maintenance; • Prepare the Investigator Site File (ISF); • Perform clinical trial activities in accordance with applicable regulations, Good Clinical Practice (GCP), and protocol requirements; • Support meeting activities such as organization, planning, and minute-taking; • Provide support to clinical research associates/monitors, clinical project managers, monitor managers, and the head of operations; • Assist in identifying potential investigative sites; • Perform co-monitoring as part of training and support CRAs during site monitoring visits; • Support the clinical research monitor in the absence of the clinical project manager.
• University degree in a health-related field; • Intermediate English; • Knowledge of Good Clinical Practice (GCP), Initiation Visit, Routine Monitoring, Close-out, and site qualification; • Previous experience as a clinical research analyst or clinical project analyst in a CRO or pharmaceutical company.
• Commuter allowance (transportation voucher); • Parking (subject to availability); • Health insurance with no monthly premium for the employee, with co-payments for tests and consultations; • Dental plan with employee co-pay; • Life insurance at no cost to the employee; • Flexible meal/food allowance; • Access to SESC partnership benefits; • Physical wellness program — TotalPass; • Day off for healthcare professionals; • Childcare assistance (per internal policy).
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🗣️🇧🇷🇵🇹 Portuguese Required