Maryelis Acosta serves as the Regulatory Coordinator at MindScope Research, where she leverages her strong organizational and leadership abilities to oversee regulatory compliance. In her role, she ensures that all clinical research activities align with industry standards and guidelines. Her responsibilities include managing critical regulatory documents and ensuring compliance with Good Clinical Practice (GCP) regulations.

Maryelis excels in developing and implementing efficient procedures while maintaining precise regulatory records. With four years of experience in administrative and managerial roles, she has honed her skills in administrative coordination and client management. She applies this expertise to streamline regulatory processes, thereby supporting the company’s commitment to research integrity.

Known for her exceptional communication skills and attention to detail, Maryelis adeptly addresses challenges, ensuring that all regulatory submissions and documentation adhere to the highest standards. Her experience working closely with clinical teams and clients enables her to navigate complex regulatory processes with accuracy. Additionally, she is proficient in managing timelines, coordinating audits, and ensuring protocol compliance. Maryelis’s proactive approach, combined with her problem-solving abilities, ensures a smooth and compliant research environment. Her dedication to maintaining the highest standards of regulatory excellence makes her an invaluable asset to the MindScope Research team.