Hamilton Medical Research Group (HMRG) is a clinical research site in Hamilton. We run Phase II to IV drug trials for global pharmaceutical sponsors, with a small team of coordinators and physicians led by Dr. Richard Tytus.
What you’ll do
- Recruit study participants: identify and screen potential participants, and obtain informed consent.
- Schedule and coordinate participant visits as the study protocol requires.
- Run every part of the study visit, from questionnaires to sample collection, processing and shipment to the protocol.
- Plan and coordinate data collection, source documentation and data entry to our policies and ICH-GCP.
- Handle study administration: collect regulatory documents, build investigator study files and prepare ethics submissions.
What you bring
- A bachelor’s degree in a health-related field, or equivalent.
- At least 3 years of clinical or professional experience.
- At least 2 years of clinical research experience, including recruiting patients for research studies or clinical trials.
- GCP certification or equivalent, and a working knowledge of ICH-GCP guidelines.
- Certification as a Clinical Research Professional, preferred.
- An asset: knowledge of IATA shipping regulations and basic laboratory procedures, and phlebotomy or ECG skills.
- Excellent organization, time management and communication, spoken and written.
- You set your own priorities and work accurately in a busy, multitasking environment, independently with little supervision and as part of a larger team.
- Strong proficiency with Microsoft Office: Word, Excel and Outlook.
What we offer
- $35 to $45 an hour.
- Full-time, Monday to Friday, 8:00 to 4:00.
- Extended health care.
- Additional compensation based on performance.