Clinical Research Coordinator
2 weeks ago
Clinical Research Coordinator (SRI) - Evaluative Clinical Sciences Join to apply for the Clinical Research Coordinator (SRI) - Evaluative Clinical Sciences - Regular Full-time 2025-15904 role at Sunnybrook. Major Responsibilities Identifying and recruiting potential research study participants via phone or in person by conducting interviews and obtaining patient consent Reviewing patient charts to determine eligibility Arranging and booking follow-up appointments by communicating and liaising effectively with other Hospital groups Answering study participants’ questions and navigating them throughout the study by effective communications Collecting, updating and managing study and participants’ data, completing CRFs, performing data entry and preparing special reports as required by the study investigators. Assist with amendments to study documents, ICFs and SOPs for Research Ethics submissions as well as regulatory file maintenance. Additional Responsibilities Work within the larger context of SHSC and observe the Hospital’s and Research Institute’s rules and regulations, policies, procedures, practices, safety procedures and current legislation, in particular the Good Clinical Practices standards. Ensure the confidentiality of patient, employee, graduate student and Hospital information at all times. Work cooperatively and constructively with the other members of SHSC staff. Perform the above functions in a manner which reflects the Hospital’s philosophy and mission of service, while promoting and maintaining good public relations with patients, visitors and Hospital staff. Understand the requirements of the various controlling bodies, agencies and frameworks, guiding the project and conforming to those requirements including any necessary audit processes. Education, Skills and Experience At minimum, completion of bachelor’s degree in health sciences, or equivalent, required. At least two (2) years of clinical/trial coordination experience and/or one (1) year of research experience or training is preferred Excellent patient interviewing and evaluation skills Demonstrated effective communication, critical thinking, and interpersonal skills Knowledge of medical terminology in the areas of gynecology and urology is preferred. Previous word-processing, database and spreadsheet software experience, in a Microsoft Office environment, including Excel, Word, PowerPoint and Electronic Patient Record Databases Knowledge of ICH/GCP regulations and guidelines Excellent organizational and time management skills with an attention to detail Excellent interpersonal and client service skills Excellent presentation and facilitation skills Self motivated and able to work independently as well as within a team Ability to produce high quality work in accordance with Hospital standards Ability to work well under pressure and use of good judgment in assessing and responding to difficult situations Ability to maintain confidentiality and strong knowledge of clinical ethics regulations Comprehensive knowledge of hospital organizational/office practices, procedures and standards Experience working in a health care, scientific or research environment preferred. Must be flexible to work Monday to Friday within the times of from 8:00 am to 4:00 pm Qualified applicants are invited to submit a resume. We thank all applicants for their interest; however, only candidates selected for an interview will be contacted. Sunnybrook Health Sciences Centre is committed to providing accessible employment practices that are in compliance with the Accessibility for Ontarians with Disabilities Act (AODA). If you require accommodation for disability during any stage of the recruitment process, please indicate this in your cover letter. Sunnybrook Health Sciences Centre is strongly committed to inclusion and diversity within its community and welcomes all applicants including but not limited to: visible minorities, all religions and ethnicities, persons with disabilities, LGBTQ persons, and all others who may contribute to the further diversification of ideas. #J-18808-Ljbffr
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Clinical Research Coordinator
2 weeks ago
Toronto, Canada Headlands Research Full timeOverview: **The Role** Toronto Memory Program is looking for a Clinical Research Coordinator to manage clinical research protocols. This individual will work directly with the investigators, and other research staff to ensure protocol visits are being conducted according to ICH GCP guidelines. **This Clinical Research Coordinator role will be based in...
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Clinical Research Coordinator Ii
5 days ago
Toronto, Canada Centricity Research Full time**Clinical Research Coordinator II (CRC II)** **Join Us at Centricity Research!** Centricity Research is one of the largest clinical research networks in North America. We are a fully centralized Integrated Research Organization (IRO) specializing in conducting Phase I-IV clinical trials in over 35 therapeutic areas: inpatient and outpatient;...
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Clinical Research Coordinator I
3 days ago
Toronto, Ontario, Canada Centricity Research Full timeJoin Us at Centricity ResearchCentricity Research is one of the largest clinical research networks in North America. We are a fully centralized Integrated Research Organization (IRO) specializing in conducting Phase I-IV clinical trials in over 35 therapeutic areas: inpatient and outpatient; pharmaceutical, biotechnology, and medical device trials.About The...
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Research Coordinator
2 weeks ago
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Clinical Research Coordinator I
2 weeks ago
Toronto, Canada Ontario Institute for Cancer Research Full time**Position: Clinical Research Coordinator I** **Location: MaRS Centre, Toronto** **Department: OHCRN** **Reports To: OHCRN Program Manager** **Salary: Commensurate with level of experience** **Hours: 35 hours/week** **Job Type: Hybrid** **Status: Full-time, Permanent** The Ontario Institute for Cancer Research (OICR) is seeking an experienced professional...
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Clinical Research Assistant
2 days ago
Toronto, Canada North York Research Inc. Full timeNorth York Research Inc. is the Clinical Trial Division of North York Dermatology Clinic. North York Research Inc. is seeking an enthusiastic individual to join our team as a Clinical Research Assistant. This position has the potential of developing into a Clinical Research Coordinator role. **Responsibilities**: - Assist Clinical Research Coordinators in...
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Clinical Screening Coordinator
2 weeks ago
Toronto, Canada Centricity Research Full timeAventiv Research, IACT Health, LMC Manna Research, and True North Clinical Research have united to become the largest network of fully-owned and integrated clinical research sites in North America, Centricity Research. The sites that were formerly known as Aventiv operate in Ohio and Arizona and specialize in phase 1 pharmaceutical, device, and diagnostic...
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Clinical Research Recruitment Assistant
2 days ago
Toronto, Canada Headlands Research Full time**Overview**: - Toronto Memory Program, a Headlands Research site, is Canada’s largest and most experienced site for drug treatment trials in Alzheimer’s disease and related conditions. Founded in 1996, we have made significant contributions to over 100 drug treatment studies in Alzheimer’s disease. Our Medical Director, Dr. Sharon Cohen, a...
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Research Coordinator
2 days ago
Toronto, Canada Centre for Addiction and Mental Health Full timeThe Centre for Addiction and Mental Health (CAMH) is the largest mental health and addiction teaching hospital in Canada, as well as one of the world's leading research centres in its field. Our services are delivered to help transform the lives of people affected by mental illness and addictions. Our goal is to tailor treatment to each individual, providing...
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Clinical Research Coordinator
5 days ago
Toronto, Canada TheOfficeChair Full timeWe are conducting the Screening rounds and an assessment sessions on behalf of our Clients for the Clinical Research coordinator roles. If qualified, your roles and responsibilities would be as follows: **Duties**: - Coordinate and oversee clinical research studies from start to finish - Ensure compliance with study protocols, regulations, and ethical...