Clinical Research Coordinator
2 days ago
Established in 2002, the **Medical Arts Health Research Group** is committed to bringing the most advanced medical opportunities to the patients of British Columbia**.** Medical Arts is comprised of a network of sites across the province that conduct Phase II through Phase IV clinical research studies.
**Position**: Clinical Research Coordinator
**Job Summary**: The Clinical Research Coordinator (CRC) will be responsible for coordinating and facilitating various aspects of clinical research studies in compliance with applicable regulations, protocols, and institutional guidelines. The CRC will work closely with the principal investigator, research team, study participants, and external stakeholders to ensure the smooth conduct of research activities. This is an in-office position in Kamloops, B.C.
**Responsibilities**:
Oversee the recruitment, screening, and enrollment of eligible study participants.Schedule study visits, procedures, and tests in accordance with the study protocol.
Conduct patient visits, including vital signs measurements, questionnaires, ECGs, administering study interventions, and monitoring participant safety.
Collect, record, and manage accurate and complete study data, maintaining confidentiality and data integrity in accordance with GCP.
Collect, prepare, and ship laboratory samples (training provided).
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, such as site selection, contract negotiation, and initiation visits. Plus ensure compliance with start-up 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.
Maintain accurate records of study-related expenses, reconcile invoices, receipts, and financial documentation.
Liaise with research team members, investigators, sponsors, and other stakeholders to ensure effective coordination and communication throughout the study.
Coordinate and participate in research meetings and training sessions as required.
**Qualifications**:
Bachelor's degree in science, psychology, or health-related field.
Previous experience in clinical research coordination or related roles is highly desirable.
Familiarity with regulatory requirements, GCP guidelines, and ethical considerations in clinical research.
Excellent organizational, time management, and attention to detail.
Strong interpersonal and communication skills to effectively interact with study participants and research team members.
**Job Type**: Part-time
Part-time hours: 10-20 per week
**Salary**: From $20.00 per hour
Schedule:
- Day shift
**Education**:
- Bachelor's Degree (required)
Work Location: In person
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