Regional Project Lead

PSI CRO; São Paulo; Presencial; BRL 120.000 - 160.000; Tempo integral

Resumo da oferta

A leading clinical research organization is seeking a Regional Project Lead in Brazil, São Paulo to manage and coordinate project teams, ensuring the compliance and timely achievement of study milestones. The ideal candidate will have a degree in Life Sciences and significant experience in Clinical Research, particularly with site monitoring. Proficiency in English and MS Office is essential, along with strong communication and leadership skills. This is a full-time position with no remote work options available.

Qualificações

• Significant experience in Clinical Research and site monitoring.
• Experience as a Study Manager or Lead with the ability to supervise.
• Full working proficiency in English.

Responsabilidades

• Manage and coordinate activities of project teams across regions.
• Ensure compliance with industry regulations and project milestones.
• Prepare presentations and conduct training of Investigators.

Conhecimentos

Clinical Research

Site Monitoring

Communication Skills

Team Leadership

Presentation Skills

Formação académica

College / University degree in Life Sciences

Ferramentas

MS Office applications including MS Project

Descrição da oferta de emprego

The Regional Project Lead 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
• Significant experience in Clinical Research and site monitoring
• Experience as a Study Manager or Leadwith the ability to supervise project activities as a Regional Lead or equivalent
• Experience in Oncology 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 levelsTeam-building leadership and organizational skills

Additional Information

Advance your career in clinical research and lead challenging full-service projects on the country / regional level while growing with a rapid company that puts its people first! You will get hands-on involvement in every aspect of the study.

For this position PSI is not hiring individuals who require work visa for employment or continued employment now or anytime in the future.

Remote Work : No

Employment Type : Full-time

Key Skills

Cognos, Interior Design, Accounting & Finance, Environmental Science, Asic

Experience : years

Vacancy : 1