Regional Project Lead

PSI CRO

$100K — $120K *
US-AnywhereRemote in Toronto, ON
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • MPharm, RN, or degree in Life Sciences or equivalent experience.
  • Minimum 4 years of site monitoring experience, with 2 years as Lead Monitor.
  • Proven ability to supervise clinical project activities and lead teams.
  • Familiarity with oncology, gastroenterology, infectious diseases, autoimmune diseases, or rare diseases preferred.
  • Strong communication, presentation, and customer service skills.
  • Demonstrated team building, leadership, and organizational abilities.
  • Fluency in English and proficiency in MS Office, including MS Project.

Responsibilities

  • Act as primary project management contact for project teams and support services.
  • Perform study status reviews, collecting and reporting project updates.
  • Develop and maintain essential project documents and manuals.
  • Ensure project timelines and subject enrollment targets are achieved.
  • Coordinate maintenance of study-specific tracking systems.
  • Oversee site selection, startup, and contract negotiations.
  • Supervise preparation and conduct of site visits and training activities.

Benefits

  • Company focuses on employee professional development and success.
Full Job Description
In this role you will streamline activities of project teams and ensure consistency of Clinical Operations processes across North America. You will ensure meeting study milestones by project teams on a country level, report study progress to clients and global stakeholders. The scope of responsibilities will include: • Act as project management contact for the project team and PSI support services. • Perform study status review and progress reporting, collect and report project status updates. • Develop and update project planning documents, essential study documents and project manuals/ instructions. • Ensure that the project timelines and subject enrollment targets are met. • Coordinate maintenance of study-specific and corporate tracking systems. • Oversee site selection and startup, site contractual and budget negotiations. • Supervise project team and site training, perform field training of monitors tailored to the project needs. • Ensure team compliance with project-specific training matrix. • Supervise preparation, conduct and reporting of site selection, site initiation, routine monitoring and closeout visits. • Review site visit reports and ensures monitoring and reporting standards are met. • Oversee investigator and site payments. • Supervise project team preparation for study audits/ inspections and resolution of audit/ inspection findings. • Might be involved in regional project oversight for NA. Qualifications • MPharm, RN or university/college degree in Life Sciences or an equivalent combination of education, training and experience. • Minimum 4 years' site monitoring experience and at least 2 years' experience as Lead Monitor. • Experience supervising clinical project activities and leading clinical project teams. • Experience in oncology, gastroenterology, infectious diseases, autoimmune diseases, or any rare disease indication is preferable. • Communication, presentation, and customer-service skills. • Team building, leadership and organizational skills. • Full working proficiency in English. • Proficiency in MS Office applications, including MS Project. Additional Information For this position, PSI is not hiring individuals who require work visa sponsorship for employment now or in the future. Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.

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