Clinical Research Coordinator
1 week ago
**Desired skills and experience**:
- Bachelor’s degree in a health-related field
- Minimum three years of clinical research experience (or equivalent combination of education and experience); CRC certification is an asset
- Thorough knowledge of clinical research ethics, REB processes, and ICH-GCP guidelines
- Highly organized, detail-oriented, and able to manage multiple priorities in a fast-paced setting
- Excellent oral and written communication, and interpersonal skills
- Skilled at coordinating participant and clinician schedules
- Demonstrated initiative, problem-solving ability, tact, and discretion
- Experience in PTSD, chronic pain, and/or Veteran populations is an asset
- Experience in transcranial magnetic stimulation (TMS) is an asset
- Ability to work both independently and collaboratively
**Key Responsibilities**:
- Schedule study participants and clinical team members for virtual and in-person study visits
- Conduct clinical outcome measures, cognitive assessments, and questionnaires
- Administer EEG- and cognitive-based assessments (training provided)
- Administer TMS sessions (training provided)
- Liaise with the REB to maintain necessary approvals and reporting
- Support participant recruitment through community and online outreach
- Screen and consent participants according to study protocol(s)
- Maintain accurate and audit-ready documentation (e.g., screening logs, CRFs, AE/PD records)
- Ensure study conduct aligns with protocols, SOPs, ICH-GCP, REB, and sponsor requirements
- Contribute to development of study tools and documents (e.g., source documents, visit checklists and workflows)
- Communicate regularly with project team; participate in team meetings as required
- Perform other duties as assigned
**How to Apply**:
**Job Type**: Part-time
Pay: $25.00-$35.00 per hour
Expected hours: 15 - 20 per week
Work Location: Hybrid remote in Surrey, BC
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