Responsibilities

• Serve as the primary clinical point of contact for clients, ensuring effective communication and collaboration throughout the study lifecycle.
• Plan, execute, and oversee clinical studies, ensuring adherence to protocols, SOPs, ICH-GCP, and regulatory requirements.
• Develop study-related clinical documents including clinical plans and Informed Consent Form templates.
• Shape and implement country-level recruitment strategies to optimize patient enrollment.
• Lead feasibility assessments and site start-up activities to ensure timely initiation of studies.
• Guide monitoring and quality strategies to maintain high standards of clinical operations.
• Mentor Clinical Research Associates (CRAs) and partners as the team expands in the region.
• Collaborate with project management on monthly invoicing and variance management of the clinical budget.
• Identify and address any issues that arise during the study to ensure successful outcomes.

Requirements

• Bachelor’s degree in a relevant field (e.g., Life Sciences, Nursing, Pharmacy).
• Proven experience in clinical trial management, specifically in LATAM regions.
• Strong understanding of clinical trial regulations and best practices.
• Exceptional organizational and leadership skills, with the ability to manage multiple projects simultaneously.
• Excellent communication skills in English and Spanish (additional languages are a plus).
• Ability to work independently as well as part of a team in a fast-paced environment.
• Familiarity with clinical trial management systems and tools is preferred.

Benefits

• Competitive salary and performance-based bonuses.
• Comprehensive health and wellness benefits.
• Opportunities for career growth and professional development.
• Flexible working arrangements to promote work-life balance.
• Supportive and collaborative team culture.