Clinical Research Coordinator - 119425
- Cambridge, ON, Canada
Full-time
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Job details
- Job type
- Full-time
- Apply by
- Posting language
- English
- Posted
Original job description
Open to CRCs or CRNs
Therapeutic area: Cardiac
POSITION SUMMARY:
The Clinical Research Coordinator (CRC) is responsible for the coordination and administration of clinical trials under the direction of the Clinical Research Manager, the Principal Investigator and the Medical Director. The CRC will develop, implement, and coordinate research and administrative procedures for the successful management of clinical trials. The CRC will perform diverse administrative duties requiring analysis, sound judgment, and a high level of knowledge of study specific protocols.
Duties and Responsibilities:
Administratively and clinically manage an average of six to eight clinical trials Adhere to Research SOP’s
Adhere to Good Clinical Practices and the study protocols
Ensure scientific integrity of data and protect the rights, safety, and well-being of patients enrolled in clinical trials
Discuss study protocols with patients and verify the informed consent documentation Provide patient with written communication of their participation (i.e. copy of the signed informed consent)
Dispense study medication in a professional and accountable manner following protocol requirements
Perform ECGs and obtain vital signs of patients
Schedule all patient research visits and procedures consistent with protocol requirements
More about this job
Responsibilities
Coordinate and administer six to eight cardiac clinical trials, ensuring compliance with research SOPs, Good Clinical Practices, and study protocols. Support patient participation through protocol discussions, informed consent documentation, medication dispensing, ECGs, vital signs, and scheduling research visits and procedures.
Requirements
The posting is open to Clinical Research Coordinators or Clinical Research Nurses and calls for knowledge of study-specific protocols, sound judgment, and the ability to manage clinical and administrative trial duties. No specific education, years of experience, or certifications are stated.
Skills
- Clinical Trial Coordination
- Clinical Research Administration
- Good Clinical Practices
- Protocol Compliance
- Informed Consent
- Patient Safety
- Data Integrity
- Patient Communication
- Study Medication Dispensing
- Electrocardiograms
- Vital Signs Measurement
- Research Visit Scheduling
- Clinical Documentation
- Administrative Procedures
- Sound Judgment
Visa sponsorship
Not detected in the job text
Categories
- Healthcare
- Science & Research
- Administrative
Keywords
- Clinical Research Coordinator
- Clinical Research Nurse
- Cardiac Research
- Clinical Trials
- Clinical Research Manager
- Principal Investigator
- Medical Director
- Research SOPs
- Good Clinical Practices
- Study Protocols
- Scientific Integrity
- Patient Rights
- Patient Safety
- Informed Consent
- Study Medication
- Electrocardiograms
- Vital Signs
- Patient Research Visits
- Clinical Trial Administration
- Research Procedures