
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.
51 - 200 employees
Founded 1993
🚗 Transport
🤝 B2B
4 days ago
🗣️🇧🇷🇵🇹 Portuguese Required

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.
51 - 200 employees
Founded 1993
🚗 Transport
🤝 B2B
• Conduct trainings relevant to the role and keep training records up to date; • Assist with administrative aspects of clinical trials, providing support to the study team (monitors and clinical project managers); • Assist in collecting and preparing documents from research sites during the conduct of the clinical trial; • Prepare the study Trial Master File (TMF) and assist in its ongoing maintenance; • Prepare the Investigator Site File (ISF); • Conduct clinical trial activities in accordance with applicable regulations, Good Clinical Practice (GCP), and protocol guidelines; • Support meeting activities such as scheduling, planning, and preparing minutes; • Provide support to clinical research monitors, clinical project managers, the monitoring manager, and the head of operations; • Assist in identifying potential research sites; • Perform co-monitoring activities for training purposes and assist clinical research monitors during site monitoring visits; • Support the clinical research monitor in the absence of the clinical project manager.
• Bachelor's degree completed in a health-related field; • Intermediate to advanced level of English; • Knowledge of Good Clinical Practice (GCP), site initiation visits, routine monitoring, close-out, and site qualification; • Previous experience as a clinical research analyst or clinical project analyst in a CRO or the pharmaceutical industry.
• Transportation allowance; • Parking (subject to availability); • Health plan with no monthly premium for the employee; co-pay applies for tests and consultations; • Dental plan with co-pay; • Life insurance at no cost to the employee; • Flexible meal/food allowance; • Pharmacy discount program; • Synvia partnership club (educational institutions, language schools, leisure and cultural services); • SESC partnership; • Physical wellness program – TotalPass; • Day off for health professionals; • Childcare assistance (according to internal policy).
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