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Descripción de la vacante
A global biopharmaceutical solutions organization is seeking a Clinical Project Specialist based in Mexico. This role involves planning and overseeing clinical trials, ensuring regulatory compliance, managing project timelines, and collaborating with cross-functional teams. The ideal candidate has a strong background in clinical project management with at least 3 years of experience and excellent organizational skills.
Formación
Minimum of 3 years of experience in clinical project management or related field.
Strong understanding of clinical trial processes and regulations.
Experience with SOP, GCP, and country-specific regulations.
Responsabilidades
Planning, directing, creating, and communicating clinical study timelines.
Gathering input from cross-functional teams for comprehensive plans.
Overseeing and resolving operational aspects of clinical trials.
Selecting sites and vendors, negotiating contracts, and managing relationships.
Preparing clinical trial budgets and monitoring expenditures.
Conocimientos
Excellent organizational and time management skills
Strong communication and interpersonal skills
Ability to work effectively in a team environment
Proficiency in Microsoft Office Suite
Attention to detail and problem-solving skills
Ability to adapt to changing priorities
Educación
Associate's degree or higher in a related field
Herramientas
Microsoft Office Suite
Descripción del empleo
A global biopharmaceutical solutions organization is seeking a Clinical Project Specialist based in Mexico. This role involves planning and overseeing clinical trials, ensuring regulatory compliance, managing project timelines, and collaborating with cross-functional teams. The ideal candidate has a strong background in clinical project management with at least 3 years of experience and excellent organizational skills.
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