Clinical Research Coordinator

**Job Overview**: The **Clinical Research Coordinator 1** (CRC 1) is responsible for research study activities such as assisting in study planning and set-up. They will be required to follow specific requirements of study protocols, regulatory requirements, policies, Standard Operating Procedures (SOPs) and Work Instructions (WI). The CRC 1 will also be...

Apex Trials by Nutrasource is looking to hire a Clinical Research Coordinator III, with 6+ years pharmaceutical clinical research experience. The Clinical Research Coordinator (CRC) III is responsible for overseeing all research study activities, assisting in project planning and set-up, and ensuring that the site staff follow specific requirements of the...

Some responsibilities of the CRC include and are not limited to: - Work directly on site conducting clinical trails while adhering to good clinical practice (patient consent, privacy, data integrity protocols, etc.) - Accurate and timely trial data collection and reporting - Process and ship lab work - Screen, track and schedule trial patients - Organize...

Job Overview: The Clinical Research Coordinator 2 (CRC 2) is responsible for assisting with and leading research study activities, assisting in project planning and set-up, and ensuring that the clinic trial site staff follow specific requirements of the protocol, regulatory requirements, and Nutrasource policies, Standard Operating Procedures (SOPs) and...

**Job Overview**: Nutrasource is seeking **Clinical Research Coordinator 2** (CRC 2) is responsible for assisting with and leading research study activities, assisting in project planning and set-up, and ensuring that the site staff follow specific requirements of the protocol, regulatory requirements, policies, Standard Operating Procedures (SOPs) and Work...

Job Description **Position Overview** **Primary Responsibilities**: Conduct the clinical research studies according to the study protocol, ICH GCPs, and SOPs. Be knowledgeable of the protocol so that all study activities are completed correctly. Obtain written informed consent from each study participant prior to participation in the study. Screen the...

**Position Overview** Our rapidly expanding team is seeking a **Clinical Research Associate (CRA)** who can work for us on a full-time basis at Guelph, ON location. CRA is responsible for monitoring activities at the clinical sites in compliance with the protocol, ICH-GCP guidelines, applicable Federal & Local regulations including company’s Standard...

**Position Overview** Our rapidly expanding team is seeking a **Clinical Research Associate (CRA)** who can work for us on a full-time basis at Guelph, ON location. CRA is responsible for monitoring activities at the clinical sites in compliance with the protocol, ICH-GCP guidelines, applicable Federal & Local regulations including company’s Standard...

PROGRAM AREA: Primary Health EMPLOYMENT STATUS: Full Time Regular, Ongoing HOURS/WEEK: 35 hours per week Our Vision A community without barriers to health and wellbeing Our Mission We reduce health inequities by providing inter-professional primary health services and community programs, focused on our priority populations, in collaboration with...

**Department: OVC-Office of the Dean** This position is classified under the Grant & Trust Professional Group Temporary full-time from 11/11/2024 to 11/10/2027 **General Purpose** Looking to be part of a fast-paced research environment with industry leaders, supporting leading-edge research and exciting clinical trials? A core member of the Bench to...

**Position Overview** The clinical trials recruiter will also be responsible for entering basic information into secure electronic medical record software in compliance with federal and provincial privacy laws. **Primary Responsibilities** Prepare recruitment strategy plans and contingency plans to ensure recruitment goals for studies are met within...

**Position Overview** The clinical trials recruiter will also be responsible for entering basic information into secure electronic medical record software in compliance with federal and provincial privacy laws. **Primary Responsibilities** Prepare recruitment strategy plans and contingency plans to ensure recruitment goals for studies are met within...

**Job description** **Position Overview** Our rapidly expanding team is looking for a **Clinical Trial Assistant (CTA) **/ **Trial Master File Administrator** who can work for us on a full time basis, supporting our clinic located in Guelph. The role is on site in Guelph ON. The Clinical Trial Associate provides support to one or more cross functional...

**Job description** **Position Overview** Our rapidly expanding team is looking for a **Clinical Trial Assistant (CTA) **/ **Trial Master File Administrator** who can work for us on a full time basis, supporting our clinic located in Guelph. The Clinical Trial Associate provides support to one or more cross functional project teams to ensure that high...

Work Term: Permanent - Work Language: English - Hours: 30 to 40 hours per week - Education: Bachelor's degree - Experience: 1 year to less than 2 years **Work setting**: - Willing to relocate - Professional association or organization - Chemical and pharmaceutical company - Pharmaceuticals industry **Tasks**: - Maintain, update and manage health...

**Unit Summary** Step into a job that opens countless doors. As one of Canada’s largest and most diverse hospitals, we’re providing advanced care to people of all ages from across the province. You can explore advancement opportunities, take professional development courses, and stretch yourself as a leader, all at HHS. We are the largest employer in...

**Department**:Clinical Studies This position is classified under the Grant and Trust Administrative & Technical Group Temporary full-time from 09/22/2024 to 09/21/2026 **General Purpose** Reporting to a faculty member in the department of Clinical Studies, the department is seeking to hire a temporary part time Research Assistant/Technician III to assist...

Make a difference in a growing, innovative mental health organization and centre of excellence in people-centered care. Work with supportive colleagues who are passionate about improving lives and champions for quality and continuous learning. As a Nurse Education Coordinator, you will be an integral part of a collaborative team focused on delivering...

About UsRexall Pharmacy Group ULC offers a dynamic environment where pharmacists can grow professionally and personally. Our company prioritizes delivering exceptional customer service and promoting community health through our pharmacy care clinic services. We value teamwork, innovation, and ongoing education. If you're passionate about improving patient...

Job description **Position Overview** **Clinical Data Manager** Provide clinical data management support to CRO Operations group Create and review electronic case report forms (eCRF) per study specific protocols Develop, review, and maintain clinical databases Manages secure database user access Develop, document and perform validation of database...