Clinical Research Project Manager (CRA/SCRA)

Tigermed; Canada; On-site; CAD 65,000 - 90,000; Full time

Job summary

Tigermed is seeking an experienced project manager for Canada-based roles overseeing clinical studies from site selection through initiation, monitoring, and close-out. You will ensure high-quality data, on-time delivery, and budget adherence across assigned sites.

The position requires 1–3 years of CRA experience, strong knowledge of ICH-GCP and GCP, and excellent English communication. Travel to Western US is expected to support study activities and sponsor requirements.

Qualifications

• Work location is based in Canada, business travel to Western US is required;
• Bachelor degree or above in Medical, Pharmacology or Biology related major;
• Good understanding and knowledge of Good Clinical Practice and clinical trial operation processes/procedures;
• At least 1-3 years of CRA experiences;
• Good command of written and verbal English;
• Good skills on Microsoft Word, Excel, PPT and Outlook, etc.;
• Other abilities such as Communication skills/Information-gathering skills. Knowledge and/or experience in medical practice is a plus.

Responsibilities

• Planning of project activities and study timelines based on project goals and sponsor's expectations;
• Organize and lead meetings/teleconferences for study activities implementation, monitor progress of each CRA responsible sites, and assess overall status of the project;
• Develop the project management plan, monitoring plan etc as required for the study;
• Develop study specific tools/forms, study templates as required for the study;
• Develop and manage project budget;
• Order and ensure all clinical supplies are adequate for all sites throughout the study period;
• Ensure all team members have timely access to appropriate systems and tools, if applicable (e.g. IVRS, eCRF);
• Organize and conduct site feasibility visits and make recommendations for final approval;
• Track study progress and ensure project is conducted according to the plan;
• Communicate to monitors new study information, timelines and goals;
• Submit the weekly project report to management;
• Study site selection, initiation (SIV) and clinical monitoring;
• Perform prestudy visit to ensure eligible sites are selected according to sponsor criteria;
• Prepare and conduct SIV to ensure adequate study training for site staff;
• Provide ongoing training to site staff with regards to ICH-GCP, GCP, study protocol;
• Ensure timely collection of essential documents in compliance with protocol and regulations at study startup, during and at study close-down;
• Finalize budget and obtain signed contract from site, prior to site initiation visit;
• Provide guidance and training to entry-level CRA/CRA I/CRA II in collaboration with Line Manager.

Skills

English proficiency

Communication skills

Education

Bachelor's degree or above in Medical, Pharmacology or Biology

Tools

Microsoft Word

Excel

PowerPoint

Outlook

Job description

Tigermed is seeking an experienced project manager for Canada-based roles overseeing clinical studies from site selection through initiation, monitoring, and close-out. You will ensure high-quality data, on-time delivery, and budget adherence across assigned sites.

The position requires 1–3 years of CRA experience, strong knowledge of ICH-GCP and GCP, and excellent English communication. Travel to Western US is expected to support study activities and sponsor requirements.