Clinical Monitoring Associate I

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Clinical Monitoring Associate I based in Brazil.

This role supports clinical trial operations across multiple phases of drug development, contributing directly to the quality, compliance, and success of studies that advance treatments for patients with chronic and critical illnesses. You will be involved in both remote and on-site monitoring activities, ensuring adherence to regulatory requirements, Good Clinical Practice (GCP), and study protocols. The position combines hands-on clinical research support with coordination between investigative sites, CRAs, and project teams in a global CRO environment. You will contribute to study start-up, monitoring activities, and data quality assurance while gaining exposure to end-to-end clinical trial execution. This is an excellent opportunity for early-career clinical research professionals seeking growth in a structured, mission-driven organization. The environment is collaborative, international, and focused on improving patient outcomes through high-quality research.

Accountabilities

• Perform in-house and remote monitoring activities for clinical trials, ensuring compliance with applicable regulatory requirements, SOPs, and study protocols.
• Support on-site monitoring, co-monitoring, and study close-out activities under the supervision of Clinical Research Associates (CRAs).
• Assist with study start-up activities, including site selection, feasibility support, and pre-study visits to evaluate potential investigative sites.
• Collect, review, track, and file essential regulatory documents and contribute to TMF/eTMF reconciliation activities.
• Conduct remote monitoring of eCRF-based studies, including query generation, follow-up, and resolution tracking with study sites.
• Support the preparation of monitoring visit materials, including visit packets and documentation for CRA-led site visits.
• Maintain study tracking tools covering visit reports, deviations, SAEs, and regulatory safety documentation.
• Communicate with investigative sites to ensure timely resolution of queries, action items, and data discrepancies.
• Assist with study-specific administrative tasks and provide operational support to CRA and project teams.
• Participate in training activities for internal teams and investigative site staff when required.

Requirements

• 1+ year of experience in clinical research, healthcare, pharmaceuticals, or a related scientific field.
• Bachelor’s degree in Nursing, Pharmacy, Health Sciences, Biology, or a related allied health discipline.
• Familiarity with clinical trial processes, medical terminology, and pharmaceutical research environments.
• Understanding of Good Clinical Practice (ICH-GCP) and general regulatory requirements is preferred.
• Strong communication skills, both written and verbal, with the ability to interact professionally with site staff and internal teams.
• Strong organizational skills with attention to detail and ability to manage multiple tracking and documentation tasks.
• Ability to work independently while also collaborating effectively within cross-functional project teams.
• Comfortable using computer systems, databases, and clinical trial software tools.
• Good time management, problem-solving, and decision-making abilities in a regulated environment.
• Willingness to learn and grow within a structured clinical research career path.

Benefits

• Opportunity to build a long-term career in global clinical research and clinical operations.
• Exposure to international clinical trials across multiple therapeutic areas.
• Structured mentoring programs and professional development pathways.
• Hybrid or flexible working arrangements depending on project needs.
• Inclusive, collaborative, and globally distributed work environment.
• Continuous training and learning opportunities in clinical research and regulatory standards.
• Participation in impactful work contributing to life-changing medical treatments.
• Strong emphasis on work-life balance and employee well-being.

How Jobgether works: We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team. We appreciate your interest and wish you the best!  Why Apply Through Jobgether?    Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time.     #LI-CL1