Clinical Research Associate

**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...

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...

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...

**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...

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...

**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 potential study...

**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...

**JOB TITLE: Research and Community Planning Associate** **PROGRAM AREA: Corporate** **EMPLOYMENT STATUS: Contract (13 months), full-time** **HOURS/WEEK: 35** **Our Vision** A community without barriers to health and wellbeing. **Our Mission** We reduce health inequities by providing interprofessional primary health services and community programs,...

**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...

**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...

The CRC Program is one of Canada’s most prestigious Research Chair programs. This CRC position is associated with the Natural Sciences and Engineering Research Council (NSERC) which is the major federal agency responsible for funding natural sciences and engineering research in Canada. The program is designed to attract leading scientists and scholars. A...

**Position Title / Rank**:Assistant or Associate Professor in Veterinary Clinical Pathology** **Department**:Pathobiology**: ***: **Position Description**:** AD24-33** In an engaging, collegial and supportive atmosphere, the incumbent will share in teaching DVM and graduate students, including trainees in applied programs in the discipline of clinical...

**Job Overview**: The **Quality Control (QC) Lead Associate** is responsible for reviewing, identifying and assists in addressing staff Good Documentation Practice issues, study information discrepancies, and SOP and Study Protocol deviations. The QC Associate reviews study source documents ensuring compliance with the protocol and ensures potential Quality...

**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...

**Fill your schedule with the support of an established clinic.** As a Clinical Social Worker associate at Natural Choice Medical Clinic, you would have access to a fully accessible clinic space situated in a medical building with a coffee shop, pharmacy, doctors offices and additional complementary medical services. These referral sources are an excellent...

**Company Description** position is in the WTS Center of Excellence (COE) for membrane development in Guelph, Ontario, Canada, and will help drive our new product introduction (NPI) growth programs globally. The Lead Researcher will invent and develop new and improved ion exchange (IX) membranes that result in new products or processes that are best-in-class...