Clinical Research Technician
About the role
Position Summary The Clinical Research Technician supports Phase I and Bioequivalence studies by performing clinical procedures, collecting and processing samples, maintaining accurate study documentation, and assisting with subject monitoring in compliance with study protocols and GCP guidelines.
Duties And Responsibilities
- Review study protocol and participate in the protocol training meeting prior to performing any study- related activities.
- Perform ECGs and vital sign assessments.
- Perform compliance checks on study subjects.
- Collect/process blood, urine and other specimens as required.
- Perform drug/cotinine screening, alcohol tests, and blood and urine pregnancy tests.
- Obtain body measurements including height and body weight and calculate Body Mass Index (BMI).
- Perform catheter insertion and removal.
- Collect, handle, and process PK samples in accordance with study procedures.
- Process and bundle lab samples and assist with shipping as required by manager/supervisor.
- Assist in drug administration by performing hand and mouth checks and verification.
- Serve and/or monitor meals.
- Maintain accurate, complete, legible and timely data entry (both digital and paper-based).
- Perform screening reception duties as required, including but not limited to ID verification, recording of demographic information (Medical Screening staff only).
- Maintaining confidentiality and privacy of study participant data.
- Verifying calibration and expiry dates of clinic equipment, supplies and medications.
- Perform data review of the source and/or other related documents as required.
- Write, compile and/or review source documentation forms.
- Performs other tasks and projects as assigned.
- Conduct Clinical staff training as qualified and/or required by supervisor/manager.
Qualifications
- Completion of Medical Technology Diploma, or equivalent.
- 1-2 years’ work experience in a CRO (preferably in conducting Phase I/Bioequivalence clinical trials) is an asset.
- 1-2 years of recent phlebotomy and ECG experience an asset.
- A minimum of 1 year experience/training in a basic laboratory setting.
- Flexible hours depending on business requirements.
- Rotating shifts and weekend requirements.
PI280867542
About HEALWELL AI (TSX: AIDX)
HEALWELL AI is a healthcare technology company focused on AI and data science for preventative care. Our mission is to improve healthcare and save lives through early identification and detection of disease. As a physician-led organization with a proven management team of experienced executives, HEALWELL AI is executing a strategy centered around developing and acquiring technology and clinical sciences capabilities that complement the company’s roadmap.
Clinical Research Technician
About the role
Position Summary The Clinical Research Technician supports Phase I and Bioequivalence studies by performing clinical procedures, collecting and processing samples, maintaining accurate study documentation, and assisting with subject monitoring in compliance with study protocols and GCP guidelines.
Duties And Responsibilities
- Review study protocol and participate in the protocol training meeting prior to performing any study- related activities.
- Perform ECGs and vital sign assessments.
- Perform compliance checks on study subjects.
- Collect/process blood, urine and other specimens as required.
- Perform drug/cotinine screening, alcohol tests, and blood and urine pregnancy tests.
- Obtain body measurements including height and body weight and calculate Body Mass Index (BMI).
- Perform catheter insertion and removal.
- Collect, handle, and process PK samples in accordance with study procedures.
- Process and bundle lab samples and assist with shipping as required by manager/supervisor.
- Assist in drug administration by performing hand and mouth checks and verification.
- Serve and/or monitor meals.
- Maintain accurate, complete, legible and timely data entry (both digital and paper-based).
- Perform screening reception duties as required, including but not limited to ID verification, recording of demographic information (Medical Screening staff only).
- Maintaining confidentiality and privacy of study participant data.
- Verifying calibration and expiry dates of clinic equipment, supplies and medications.
- Perform data review of the source and/or other related documents as required.
- Write, compile and/or review source documentation forms.
- Performs other tasks and projects as assigned.
- Conduct Clinical staff training as qualified and/or required by supervisor/manager.
Qualifications
- Completion of Medical Technology Diploma, or equivalent.
- 1-2 years’ work experience in a CRO (preferably in conducting Phase I/Bioequivalence clinical trials) is an asset.
- 1-2 years of recent phlebotomy and ECG experience an asset.
- A minimum of 1 year experience/training in a basic laboratory setting.
- Flexible hours depending on business requirements.
- Rotating shifts and weekend requirements.
PI280867542
About HEALWELL AI (TSX: AIDX)
HEALWELL AI is a healthcare technology company focused on AI and data science for preventative care. Our mission is to improve healthcare and save lives through early identification and detection of disease. As a physician-led organization with a proven management team of experienced executives, HEALWELL AI is executing a strategy centered around developing and acquiring technology and clinical sciences capabilities that complement the company’s roadmap.