CRA/SCRA-Canada

Job summary

Responsible for project and study site management from selection through close-out in compliance with SOPs and GCP standards. Ensures high-quality data generation while managing project timelines, budgets, and clinical supplies.

Job details

1. Job Purpose: This position is responsible for project management and study site management from site selection to initiation until monitoring and close-out of assigned clinical study studies in accordance with Tigermed or sponsor Standard Operating Procedures (SOPs), International Conference on Harmonization Good Clinical Practice standard (ICH-GCP), Clinical Practice standard (GCP) and other applicable regulations; The position is responsible for ensuring that all data generated by the assigned sites is of high quality, on time and within budget. 2. Responsibilities: Planning of project activities and study timelines based on project goal andsponsor's expectation; Organize and Lead meeting/teleconferences for study activities implementation(e.g. investigator meeting, project review meeting etc), monitoring the progressof each CRA responsible sites, and assessing overall status of the project; Develop the project management plan, monitoring plan etc as required for thestudy; Develop study specific tools/forms, study templates as required for the study; Develop and manage project budget; Order and ensure all clinical supplies (including drug and nondrug) areadequate for all sites throughout the study period; Ensure all team members have timely access to appropriate systems and tools, ifapplicable (e.g. IVRS, eCRF etc); Organize and conduct site feasibility visits according to guidelines and makerecommendation for final approval; Track study progress and ensure project is conducted according to the plan; Communicate to monitors new study information, study timelines and goals,study requirements. Responsible for raising overall project specific issues tomanagement (e.g. Project Director, Senior Management); Submit the weekly project report to management (e.g. Project Director, SeniorManagement); Study site selection, initiation (SIV) and clinical monitoring; Perform prestudy visit to ensure eligible sites are selected according to sponsorsite selection criteria, including but not limited to adequate resources andexperience; Prepare and conduct SIV to ensure adequate study training for relevant site staffto proceed with study start and conduct in compliance with protocol andrelevant regulations; Provide ongoing training to site staff with regards to ICHGCP, GCP, studyprotocol, and requirements; Ensure timely collection of essential documents in compliance with protocol andregulations at study startup, during and at study closedown. Maintain andupdate these documents in investigator files, trial master files; Finalize budget and obtain signed contract from site, prior to site initiation visit; Provide guidance and training to entrylevel CRA/CRA I/CRA II in collaborationwith Line Manager. Submit the weekly project report to management (e.g. Project Director, Senior Management); Study site selection, initiation (SIV) and clinical monitoring; Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but not limited to adequate resources and experience; Prepare and conduct SIV to ensure adequate study training for relevant site staff to proceed with study start and conduct in compliance with protocol and relevant regulations; Provide ongoing training to site staff with regards to ICH-GCP, GCP, study protocol, and requirements; Ensure timely collection of essential documents in compliance with protocol and regulations at study start-up, during and at study close-down. Maintain and update these documents in investigator files, trial master files; 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. 3. 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. Welcome passion and creative ideas' friends! Look forward to receiving your profiles.

What you’ll do

Responsible for project and study site management from selection through close-out in compliance with SOPs and GCP standards. Ensures high-quality data generation while managing project timelines, budgets, and clinical supplies.

Requirements

Requires a Bachelor's degree in Medical, Pharmacology, or Biology with 1-3 years of CRA experience. Must have a strong understanding of GCP and be able to travel to the Western US.

Listed skills

• Microsoft Excel · Preferred
• Microsoft Word · Preferred
• Communication Skills · Preferred
• Project management · Preferred
• Microsoft Outlook · Preferred

Other relevant skills

Identified from the job description. Confirm important requirements above.

• Project Management
• Study Site Management
• Clinical Monitoring
• ICH-GCP
• Site Selection
• Site Initiation Visits
• Budget Management
• Clinical Trial Operations
• Microsoft Word
• Microsoft Excel
• Microsoft PowerPoint
• Microsoft Outlook
• Communication Skills
• Information-gathering Skills

Job areas

• Science & Research
• Healthcare
• Management & Leadership
• Manufacturing
• Consulting

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