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Senior Clinical Project Analyst
Location
Brazil
Posted
2 days ago
Salary
0
Seniority
Senior
Job Description
Senior Clinical Project Analyst
SYNVIA
• 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.
Job Requirements
- 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.
Benefits
- 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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