Clinical Regional Project Lead

Psi CRO; Lima Metropolitana; Híbrido; PEN 302.000 - 437.000; Jornada completa

Descripción de la vacante

PSI CRO is seeking a Regional Project Lead to oversee clinical trial activities across designated countries. You will coordinate project teams, ensure regulatory compliance, and drive study milestones with a strong focus on quality and timelines.

The role requires extensive experience in Clinical Research, on-site monitoring, and leadership across multi-country operations, including experience in Oncology. Excellent English communication and MS Office/MS Project proficiency are essential.

Formación

• Degree in Life Sciences or equivalent and relevant experience.
• Experience in Clinical Research and on-site monitoring.
• Experience monitoring within the US.
• Experience as Study Manager/Clinical Trial Manager with regional lead responsibilities.
• Experience in Oncology is required; GI preferred.
• Full working proficiency in English; strong communication skills.

Responsabilidades

• Oversee, manage and coordinate project teams in designated countries and regions.
• Ensure planning, implementation and management of projects in compliance with ICH-GCP and regulatory documents.
• Lead study status reviews and progress reporting as delegated by Project Manager.
• Coordinate site activation, monitoring visits and closeout activities.
• Manage KPIs, timelines, enrollments, and budget-related reporting.
• Supervise team performance, training, and resource allocation.

Conocimientos

Project management

Leadership

Team leadership

Communication

English proficiency

MS Office

MS Project

Stakeholder management

Educación

Life Sciences degree

Herramientas

MS Office

MS Project

Descripción del empleo

PSI is a leading Contract Research Organization with more 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.

Job Description

The Regional Project Lead is a senior level clinical trial manager who oversees, manages, and coordinates activities of project teams in designated countries and ensures consistency of Clinical Operations processes across regions. They ensure meeting study milestones are met by the project team on a country and regional level.

• Ensures planning, implementation, and management of projects in compliance with industry regulations, ICH-GCP, essential study documents, and applicable controlled documents (e.g., PSI QSDs or Sponsor QMS documents)
• Acts as primary or secondary project management contact for the project team and PSI support services in designated countries
• Performs study status review and progress reporting (if delegated by the Project Manager)
• Collects and reports project status updates for designated regions, both internally and externally
• Develops and updates project planning documents, essential study documents and project manuals/ instructions
• Manages and reports on Key Performance Indicators (KPIs) for designated countries and clinical project team members
• Ensures that the project timelines and subject enrollment targets are met in designated countries
• Coordinates maintenance of study-specific and corporate tracking systems
• Coordinates site contractual startup and budget negotiations
• Establishes communication lines within the project teamand supervises clinical project team members’ performance
• Identifies, escalates and resolves resourcing and performance issues
• Conducts and supervises therapeutic area training of the project team (if delegated by the Project Manager)
• Prepares presentations and conducts training of Investigators
• Ensures team compliance with project-specific training matrix
• Performs field training of Monitors tailored to the project needs
• Supervises preparation, conduct and reporting of site selection, site initiation, routine monitoring and closeout visits
• Oversees investigator and site payments, as well as CRF data retrieval/ upload and monitoring and the query resolution process
• Supervises project team preparation for study audits/ inspections and resolution of audit/ inspection findings
• Coordinates conduct of supervised monitoring visits
• Reviews site visit reports and ensures monitoring and reporting standards are met
• Coordinates preparation of initial and follow-up Regulatory and Ethics Committee submissions and notifications
• Oversees the safety information flow and participates in feasibility research
• Reviews/approves project related expenses and timesheets (if delegated by the Project Manager)

Qualifications

• College/University degree in Life Sciences or an equivalent combination of education, training & experience is required
• Prior experience in Clinical Researchand on-site monitoring is required
• Prior experience monitoring within the US
• Experience as a Study Manager/Clinical Trial Managerwith theability to supervise project activities as a Regional Lead or equivalent is required
• Experience in Oncology is required
• Experience in GI is preferred
• Full working proficiency in English
• Proficiency in MS Office applications, including MS Project
• Communication, presentation and customer-service skills
• Ability to negotiate and build relationships at all levels
• Team building, leadership and organizational skills

Additional Information

Advance your career in clinical research, coordinating a variety of tasks and learning new things while growing with a rapid growing company that puts its people first.

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