Requirements

Additional Requirements

Excellent interpersonal and written and spoken English communication skills, with the ability to effectively interact with clients, internal teams, and stakeholders at all levels.
Solid general understanding of clinical trial processes, including biostatistics, medical writing, and data management practices, with expertise in at least one functional domain.
Proficiency in project management tools and software.
Proven ability to manage multiple projects simultaneously while maintaining high standards of quality and attention to detail.
Effective critical thinking skills.
Strong organizational and time management skills.
Problem-solving skills and the ability to adapt to changing project needs.
Experience with budget planning and management.
Experience in client management and a demonstrated ability to build and maintain strong client relationships.
Strong leadership and team management abilities, with a track record of successfully leading cross-functional teams.
In-depth knowledge of biometrics processes, including statistical analysis, data management, and clinical trial reporting.
Solid understanding of clinical trial documents (protocols, statistical analysis plans, CRFs, study reports) and processes.
Solid understanding of regulatory guidelines (ICH-GCP) and industry standards.
Strong knowledge of office software (Microsoft Office).
Prior experience (6+ years) in project management within the biopharmaceutical industry or CRO setting. Significant experience in at least one biometrics functional domain is preferred. Functional leading experience can be considered in lieu of direct project management experience.

Senior Biometrics Project Manager - Latin America

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