Clinical Research Coordinator/rater

2 months ago

Nanaimo, Canada Medical Arts Health Research Group Full time

Overview

**Responsibilities**:

- Manage and coordinate the studies from initiation to completion
- Oversee recruitment, screening, and enrollment of eligible study participants.
- Schedule study visits, procedures, and tests in accordance with the study protocol.
- Conduct pre-screening questionnaires by phone.
- Conduct patient visits, including vital signs measurements, questionnaires, ECGs, administering study interventions, and monitoring participant safety.
- Administer psychiatric assessments: MINI, C-SSRS, BPRS, CGI-S.
- Collect, prepare, and ship laboratory samples (training provided).
- Collect, record, and maintain study data accurately.
- Conduct phlebotomy procedures as required.
- Analyze and interpret study results.
- Supervise research staff and ensure compliance with protocols.
- Assist in the preparation of regulatory documents and submissions.
- Communicate with study participants, healthcare providers, and sponsors.
- Utilize medical terminology effectively in documentation.
- Ensure compliance with study procedures, regulatory requirements, and ethical guidelines.
- Address participant inquiries, concerns, and adverse events promptly, ensuring appropriate documentation and reporting.
- Assist in the initiation and implementation of new clinical research studies, including trainings, regulatory submissions, and obtaining necessary approvals.
- Coordinate study start-up activities, ensuring compliance with requirements and timelines.
- Develop and implement strategies for community outreach initiatives to promote awareness and participation in clinical research studies.
- Establish relationships with community organizations, healthcare providers, and relevant stakeholders to foster collaboration and engagement.
- Liaise with research team members, investigators, and sponsors to ensure effective coordination and communication throughout the study.
- Coordinate and participate in research meetings and training sessions as required.

Psychometric Assessments Breakdown
- MINI 7.0.2: Administer the Mini International Neuropsychiatric Interview to assess psychiatric disorders accurately.
- CGI-S (Clinical Global Impression - Severity): Rate the severity of a patient's illness based on observed and reported symptoms.
- MGH ATRQ (Massachusetts General Hospital Antidepressant Treatment History): Evaluate a patient's history of antidepressant treatment.
- C-SSRS (Columbia-Suicide Severity Rating Scale): Assess the severity of suicidal ideation and behavior.

**Qualifications**:

- Bachelor's or Master's degree in psychology, counseling, science, or a health-related field.
- Previous experience with psychological assessments and psychiatric scales.
- Experience working in mental health settings.
- Excellent organization, time management, computer skills, and attention to detail.
- Strong interpersonal and communication skills to effectively interact with study participants and team members.
- Previous experience in clinical research coordination or related roles is highly desirable.
- Familiarity with regulatory requirements, GCP guidelines, and ethical considerations in clinical research is an asset.

Job Type
- Part-time
- Expected hours: 10-20 hours

**Job Type**: Part-time

Pay: $30.53-$50.00 per hour

Expected hours: 10 - 20 per week

Flexible language requirement:

- French not required

Schedule:

- Weekends as needed

Work Location: In person

Expected start date: 2024-09-23

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