Senior Associate I, TMF Operations

📋 Description

• Oversee TMF activities across studies for compliant docs
• Collaborate with project teams and sponsors on TMF needs
• Manage quality control, tracking, and follow-up on issues
• Assist creation/maintenance of study TMF quality docs
• Prepare/present TMF KPIs and data trends to teams
• Support regulatory inspections and audits as needed

🎯 Requirements

• University degree preferred in Life Sciences or related field
• 1–3 years of relevant clinical research/regulatory exp
• Strong understanding of clinical research principles and TMF mgmt
• Excellent planning, organizational, and prioritization skills
• Clear written/verbal communication with stakeholders
• Analytical, solution-focused with regulatory compliance

🎁 Benefits

• Full-time remote position with flexibility for professionals based in Brazil
• Opportunity to contribute to impactful clinical research programs
• Collaboration with global teams across clinical research functions
• Inclusive environment focused on collaboration and growth
• Opportunities to develop TMF ops, compliance, and trial mgmt
• Access to professional development and career growth