Clinical Regional Project Lead

🕒 August 4

🇨🇦 Canada – Remote

💵 $140k - $155k / year

⏰ Full Time

🟠 Senior

👻 Ghost score 6%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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PSI CRO AG

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Founded 1996

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

PSI CRO AG is a global contract research organization (CRO) that specializes in conducting clinical trials. The company focuses on delivering pivotal Phase 2 and 3 clinical trials across various therapeutic areas, including Inflammatory Bowel Diseases, Oncology, Hematology, Infectious Diseases, Multiple Sclerosis, and Rare Diseases. PSI utilizes a proprietary technology platform for clinical trial planning and financial tracking to ensure trials are conducted on time and within budget. The company is recognized for its expertise, quality, compatibility, and reliability, having been awarded the CRO Leadership Awards for multiple consecutive years.

📋 Description

• Streamline activities of project teams and ensure consistency of Clinical Operations processes across the Asia Pacific region • Ensure study milestones are met by project teams at country level • Report study progress to clients and global stakeholders • Act as project management contact for project teams and PSI support services • Review study status and report progress • Collect and report project status updates • Develop and update project planning documents, essential study documents, project manuals and instructions • Ensure 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, including field training of monitors • 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 ensure monitoring and reporting standards are met • Oversee investigator and site payments • Supervise project team preparation for study audits and inspections and resolution of findings • Participate in regional project oversight for APAC as needed

🎯 Requirements

• MPharm, RN, or university/college degree in Life Sciences, or equivalent combination of education, training and experience • Minimum 4 years of site monitoring experience • At least 2 years of experience as a Lead Monitor • Experience supervising clinical project activities and leading clinical project teams • Experience in oncology, gastroenterology, infectious diseases, autoimmune diseases, or rare disease indications preferred • 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

🏖️ Benefits

• Remote work • Professional development and investment in career success • Stable and secure workplace • Inclusive culture and welcoming environment