Research I

The Clinical Trials Unit is recruiting a Research Coordinator to provide support for clinical research trials. You will be assigned to the Gastrointestinal and Liver Research Group (GILDR) located at the Zeidler Ledcor Centre.The responsibilities of this position includes recruitment of participants in clinical research studies, training of new research staff, developing inservice training for all research staff, updating standard operating procedures and policies, quality assurance of clinical trial documentation. This position may also be involved in obtaining informed consent, participants study visits, collecting and reporting clinical trial data, and reviewing/filing of study documents in the Investigator Trial File. As a Research Coordinator, you will require exceptional organizational skills that are necessary to ensure trial information is timely, accurate, valid and to the sponsor's satisfaction. A main component of this role is to ensure that participants are recruited to active studies in a timely manner, clinical research staff are trained on each protocol and that studies are run according to the protocol and Health Canada regulations. Working under limited supervision, you will perform diversified duties requiring independent judgement and confidentiality. To be successful in this role, you will require excellent problem-solving skills and the ability to work in a team environment. You must be able to handle multiple demands with short timelines while remaining sufficiently flexible to accept new workload as necessary.

As a Research I, you will be working with research teams which are generating and disseminating new knowledge that assists with advancing the understanding of health disciplines and various health and medical concerns. Working under the guidance of the principal investigator, you will be responsible for preparing and submitting research documents, collecting and reviewing a variety of information related to the study, and monitoring study compliance. You will also assist with the recruitment of study participants and initiate consenting of study and/or trial participants and may complete lab work to support research activities.

Diploma or degree in a health or science related field. Registration with applicable professional association or college where required.

Minimum 3-5 years of experience working in a clinical research environment with current experience recruiting and enrolling study participants in Hepatology and Gastroenterology clinical trials. Experience in training of new clinical trial staff in study procedures. Knowledge of clinical trial regulations and guidelines (ICH-GCP training, Health Canada and FDA). Experience with electronic data capture and database programs. Knowledge of medical terminology. Experience working with Pharmaceutical sponsors and clinical research organizations. Netcare & Connect Care Research Training and Phlebotomy experience. Fibroscan certification required.

As required.