CRA - all levels

To join our team, we are looking for professionals who want to contribute to our mission of improving lives of more and more people . If you have an innovative profile, think outside the box, and enjoy working in a modern and dynamic environment, this position is for you. Come join us on this journey. #JoinSynvia

Contamos com você para: General On-Site Monitoring Responsibilities, including routine monitoring visits and close-out of clinical sites; Conduct pre-study visits such as SQV – Site Qualification Visit and SIV – Site Initiation Visits; Ensure the integrity of the data submitted on Case Report Forms (CRFs) by carefully reviewing source documents; Perform CRF review, including generating and resolving queries, to ensure data quality; Maintain study files, ensuring audit readiness at the site level; Prepare and provide FUP (Follow-Up) letters and reports within the established deadlines for respective monitoring visits; Track and follow up on Serious Adverse Event (SAE) reporting, including producing reports, narratives, and following up on SAEs; Track and follow up on Deviation Reports according to the study's plan; Act as the focal point of communication between the site team, project manager, and vendors to resolve any arising issues. Liaise with vendors and perform other duties as assigned; Ensure that the conduct of clinical trial activities complies with current ethical regulations, Good Clinical Practices, and protocol guidelines; Maintain accounting and control of investigational products and other trial materials/supplies; Travel, including air travel, will be required and is an essential function of the job. Prepare accurate and timely trip reports and expense reimbursements.

O que buscamos: Complete higher education in Pharmacy, Biomedicine, or Nursing; Good Practices in Clinical Research, Initiation Visit, Routine, Close Out, and center qualification; Intermediate English; Minimum of 2 years' experience in clinical research as a clinical research analyst, or previous experience as a research center coordinator.

Unidade de trabalho: Sede Administrativa: Paulínia/SP - Home Based . What benefits we offer you: Transportation allowance. Parking (subject to availability). Heath Insurance with no monthly cost to employee, with co-participation for exams and medical consultations. Dental plan with monthly co-participation. Life Insurance. Food/Meal allowance. Pharmacy benefit. Vaccination program. Synvia Partnership Club (Education Institutions, Language Learning, Leisure and Cultural Activities). Hybrid Work Model (to be aligned with leadership). SESC Partnsership; Physical health program - TotalPass. Heath Professional - Day off. Nursery assistance (as per internal policy).