RTSM Project Lead — Global Clinical Trials (US/CA)

Worldwide Clinical Trials; Quebec; On-site; CAD 100,000 - 199,000; Full time

Job summary

Worldwide Clinical Trials in Canada is seeking an RTSM Specialist to lead the successful implementation of RTSM systems in collaboration with sponsors and internal teams. You will manage projects from award through decommissioning, ensuring timeliness and budget adherence.

You will coordinate study communications, prepare status reports and agendas, and travel for Investigator Meetings when required. A strong background in RTSM design, randomization, and drug supply is essential.

Qualifications

• Educated to degree level in a relevant discipline or able to demonstrate equivalent experience.
• Minimum 2 years RTSM experience.
• Minimum 1 year project management experience.
• Minimum of 5 years experience within CRO/pharma environment.
• CRO or Pharmaceutical experience required.
• Familiar with RTSM topics, including RTSM study design, randomization methodologies, and just-in-time drug supply.
• Understanding of clinical trials, blinding, patient safety, data integrity and associated regulations.
• Proven ability to manage delivery of RTSM solutions deployed in clinical trials.

Responsibilities

• Provide project management oversight from award to RTSM decommissioning, including oversight and accountability of deliverables and timelines and completion of work to Worldwide SOP standards
• Communicates information on applicable RTSM project activities to stakeholders, including internal and sponsor study teams. Serves as the escalation point of contact for all RTSM assigned study-related project issues
• Overall accountability for coordination and timely delivery of RTSM project communications including study status reports, meeting agendas and minutes and scheduling project calls
• Willingness to travel and attend Investigator Meetings or other types of project related meetings when required
• Responsible for overall RTSM project budget and ensuring accurate vendor work orders for assigned studies
• Responsible for overall RTSM study design, as well as writing or reviewing and approving User Requirements Specification (URS)

Skills

Communication

Client-facing

Office software

Self-motivated

Attention to detail

Multitasking

Education

Degree or equivalent experience

Job description

Worldwide Clinical Trials in Canada is seeking an RTSM Specialist to lead the successful implementation of RTSM systems in collaboration with sponsors and internal teams. You will manage projects from award through decommissioning, ensuring timeliness and budget adherence.

You will coordinate study communications, prepare status reports and agendas, and travel for Investigator Meetings when required. A strong background in RTSM design, randomization, and drug supply is essential.