Clinical Trial Manager – LATAM

🕒 July 3

🌐 Argentina, Brazil, +1 more countries – Remote

🇦🇷 Argentina – Remote 🇧🇷 Brazil – Remote 🇲🇽 Mexico – Remote

⏰ Full Time

🟠 Senior

🔴 Lead

🧪 Clinical Research

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Precision Medicine Group

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Founded 2012

💼 Consulting

🏥 Healthcare

📦 Logistics

💰 $35.2M Venture Round on 2021-03

Consulting • Healthcare • Logistics

Precision Medicine Group is a global team of experts that specializes in precision medicine, which combines advanced lab sciences, translational informatics, regulatory affairs, payer insights, and marketing communications. The company focuses on overcoming product development and commercialization challenges for pharmaceutical and life sciences clients. Their services include biomarker-driven research and development, as well as commercialization support for life science organizations from launch to product maturity. Precision Medicine Group operates through two main arms: Precision for Medicine and Precision AQ, specializing in clinical and commercial solutions respectively.

📋 Description

• Own the planning, execution, and oversight of clinical studies • Serve as the primary client contact and ensure delivery in compliance with protocol, SOPs, ICH-GCP, and regulatory requirements • Shape country-level recruitment strategies • Lead feasibility and site start-up • Guide monitoring and quality strategies • Mentor CRAs and partners as the team scales • Develop study-related clinical documents • Identify and develop training needs for CRAs and third-party vendors • Generate potential site list and drive site feasibility process • Identify risks to enrollment targets • Develop country recruitment/retention strategy • Ensure effective communication with investigators and study team • Manage clinical team expectations • Support planning and conducting investigator meetings • Oversee, support, and track submissions and approvals • Collaborate with PM, CRAs, and QA to develop CAPA plans • Assist sites, internal staff, and CRAs with the preparation for GCP audits

🎯 Requirements

• Bachelor’s degree or equivalent combination of education/experience in science or health-related field. Advanced degree preferred • Minimum of 7 years of clinical research experience or proven competencies for the position with significant clinical monitoring experience • Professional working proficiency in English required • Experience with Microsoft Office Products (Outlook, Word, Excel, PowerPoint) • Excellent communication and interpersonal skills to effectively interface with others in a team setting • Excellent organizational skills, attention to detail, and a customer service demeanor • Ability to travel domestically and internationally including overnight stays

🏖️ Benefits

• Career growth opportunities • Opportunities to build teams • Define processes • Influence culture • Step into broader leadership and project management responsibilities