Clinical Research Coordinator
4 days ago
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 potential study participants according to the protocol’s inclusion and exclusion criteria.
Schedule study participant visits as per protocol.
Perform delegated protocol specific activities completely and accurately.
Obtain vital signs as required per protocol (i.e. blood pressure, temperature, heartrate, respiratory rate, weight & height).
Provide lifestyle adherence counseling & general training / education to study participants, as required by protocol.
Obtain all necessary documentationas required by the protocol.
Monitor and report all adverse experiences and abnormal results to the Investigator, CRO and IRB if necessary.
Create & complete source documents and any other research documents required for the successful conduct of a clinical research study.
Ensure ISF is kept current for trial.
Liaises with the Principal Investigator and Site Director during course of trial.
Enter data into EDC and query resolution.
Maintains an attitude and philosophy consistent with the Company's standards.
**Core Competencies**:
Knowledge of medical terminology
Knowledge of general research procedures and regulatory requirements
Strong communication and interpersonal skills
Detail oriented with exceptional organizational skills
Ability to work in a team
Proficiencywith MS Office suite
**Qualifications**:
Bachelor of Science degree or post-grad diploma
Minimum 1-2 years of clinical research training or experience
GCP certification desirable
CCRA / CCRP / ACRP certification preferred
Previous experience with phlebotomy and intravenous catheters is an asset
**Must be available weekday and early mornings**
**Job Types**: Part-time, Temporary, Contract
**Job Types**: Part-time, Fixed term contract, Casual
Schedule:
- 10 hour shift
- 12 hour shift
- 8 hour shift
-
Clinical Research Coordinator
20 hours ago
Guelph, Canada Nutrasource Full time**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...
-
Clinical Research Coordinator Iii
2 weeks ago
Guelph, Canada Nutrasource Full timeApex 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...
-
Clinical Research Coordinator
1 week ago
Guelph, Canada Nutrasource Full time**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...
-
Clinical Research Coordinator
2 weeks ago
Guelph, Canada Nutrasource Full time**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...
-
Clinical Research Physician
2 weeks ago
Guelph, Canada Nutrasource Full time**Position Overview** This is a **part-time, on-site position (2-3 full days per week)** with flexibility for **occasional weekend coverage** based on study needs. Applicants **must be a physician licensed to practice medicine in Ontario** and in good standing with the **College of Physicians and Surgeons of Ontario (CPSO).** **Key Responsibilities** -...
-
Research Assistant
1 week ago
Guelph, Canada Nutrasource Full timeJob Overview: The Research Assistant is responsible for research study activities such as assisting in study planning and set-up, assisting with study participant visits and study close out activities. They will be required to follow specific requirements of study protocols, regulatory requirements, policies, Standard Operating Procedures (SOPs) and Work...
-
Clinic Coordinator
2 weeks ago
Greater Guelph Metropolitan Area, Canada AMMC Full timeCompany DescriptionAMMC is a comprehensive provider of solutions for medical professionals and clinics, offering services in management, billing, clinic setup, recruitment, marketing, and telemedicine. We deliver consulting, training, IT support, and branding strategies to help optimize and grow healthcare practices. AMMC specializes in medical office...
-
Clinical Trial Participant Recruiter
4 days ago
Guelph, Canada Nutrasource Full time**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...
-
Clinical Research Associate
6 days ago
Guelph, Canada Nutrasource Pharmaceutical and Nutraceutical Services INC Full timeWork 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...
-
Research Assistant Technician Iii
2 weeks ago
Guelph, Canada University of Guelph Full time**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...