Clinical Country & Site Associate (Clinical Trial Manager) - Sponsor dedicated

Job Description

• This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Clinical Country & Site Associate (Clinical Trial Manager) - Sponsor dedicated based in Brazil. This is a field- and site-focused clinical operations role at the heart of global clinical research execution, supporting sponsor-dedicated studies across multiple therapeutic areas. You will ensure that clinical trial sites operate in full compliance with regulatory standards, ICH-GCP guidelines, and study protocols while maintaining high-quality data integrity. The role combines on-site and remote monitoring responsibilities, requiring strong attention to detail and a proactive, problem-solving mindset. You will work closely with investigators, site staff, and cross-functional clinical teams to support study start-up, execution, and close-out activities. This position plays a critical role in safeguarding patient safety, ensuring data accuracy, and driving study performance across assigned sites. It offers exposure to complex, global clinical trials within a fast-paced, highly regulated environment where precision and communication are essential.
• Accountabilities: Conduct site qualification, initiation, monitoring, and close-out visits (on-site and remote), ensuring compliance with study protocols, ICH-GCP, Good Pharmacoepidemiology Practices, and applicable regulatory requirements. Perform ongoing site management activities, including source document verification, case report form (CRF) review, query resolution, and tracking of site performance metrics. Ensure proper informed consent processes are followed and documented, while continuously assessing patient safety, protocol deviations, and pharmacovigilance-related issues. Review Investigator Site Files (ISF), reconcile with Trial Master File (TMF), and ensure documentation accuracy, completeness, and audit readiness. Support investigational product (IP) accountability, including storage, dispensing verification, reconciliation, and compliance with blinding and labeling requirements. Act as a primary liaison with site personnel, supporting communication, training compliance, recruitment strategies, and timely resolution of site-level issues. Prepare required study documentation, including trip reports, follow-up letters, and communication logs, while ensuring timely data entry into tracking systems. Requirements: Bachelor’s degree in a life sciences, nursing, or related field, or equivalent combination of education and clinical research experience. Solid understanding of ICH-GCP guidelines, clinical trial regulations, and Good Clinical Practice standards in global research environments. Prior experience in clinical monitoring, site management, or clinical research operations (experience in sponsor- or CRO-led trials is highly desirable). Strong knowledge of clinical trial processes, including source data verification, EDC systems, and clinical documentation practices. Excellent communication and interpersonal skills, with the ability to collaborate effectively with investigators, site staff, and cross-functional teams. Strong organizational skills with the ability to manage multiple sites, prioritize tasks, and meet strict timelines in a regulated environment. Willingness to travel up to 75% and adapt to dynamic study needs and changing priorities. Benefits: Opportunity to work on global clinical trials with high scientific and regulatory impact Exposure to sponsor-dedicated studies across leading therapeutic areas Flexible work arrangement with significant field-based and remote collaboration Strong focus on professional development, training, and career progression in clinical research Participation in high-impact studies contributing to patient access and healthcare innovation Collaborative, international work environment within a leading life sciences organization
• 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
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