Responsibilities

• Provide overall support to study sites and clinical project teams engaged in clinical research studies.
• Ensure adherence to applicable protocols, standard operating procedures (SOPs), and regulatory requirements, including Good Clinical Practice (GCP) guidelines.
• Act as the primary point of contact for study sites, addressing inquiries and providing assistance throughout the study process.
• Utilize extensive site management experience to guide and mentor junior team members in site management activities.
• Perform and manage investigator recruitment activities effectively.
• Assist in the development of tools and resources to streamline communication and processes with study sites.
• Collaborate with the Clinical Monitoring management team to provide support and ensure project milestones are met.
• Contribute to the continuous improvement of clinical trial processes and site operations.

Requirements

• Bachelor’s degree in a related field; advanced degree preferred.
• Minimum of 5 years of experience in clinical research, particularly in site management.
• Strong knowledge of ICH-GCP guidelines and local regulatory requirements.
• Excellent communication and interpersonal skills, with the ability to build relationships with diverse study sites.
• Proven ability to mentor and develop junior staff members.
• Fluency in English; proficiency in Spanish and/or Portuguese is a plus.
• Strong problem-solving skills and attention to detail.

Benefits

• Competitive salary with performance-based bonuses.
• Comprehensive health and wellness benefits.
• Opportunities for professional development and training.
• Flexible work schedule with remote work options.
• Collaborative and inclusive company culture focused on innovation.
• Chance to be part of a growing team dedicated to improving patient outcomes in LATAM.