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Company | Centricity Research |
Address | Ottawa, Ontario, Canada |
Employment type | FULL_TIME |
Salary | |
Category | Internet Publishing |
Expires | 2023-07-28 |
Posted at | 10 months ago |
IACT Health, LMC Manna Research, and True North Clinical Research joined forces in late 2021 to become Centricity Research. Centricity Research is a clinical research organization with more than 40 sites, access to over 1.6 million patients, and more than 150 active investigators across Canada and the southeastern United States. Our name, Centricity Research, was purposefully chosen to signify the fact that we are customer centric. Our patient volunteers, sponsors, CROs, and physicians are the cornerstone of our business. The name Centricity Research also highlights the fact that our organization has earned a position of prominence and importance within the industry. We aim to build and nurture strong, trusting relationships with all audiences, and being customer-centric is embedded within our company culture
- To schedule study participant visits as per protocol
- Provide lifestyle adherence counseling & general training / education to study participants, as required by protocol
- To perform delegated protocol specific activities completely and accurately
- To conduct the clinical research study according to the study protocol, GCP, and the LMC Manna Research SOP/WP
- To screen the potential study participants according to the protocol’s inclusion and exclusion criteria
- To obtain vital signs as required per protocol (i.e. blood pressure, temperature, heart rate, waist measurement, weight & height)
- To obtain all necessary documentation as required by the protocol (i.e. ECG, echocardiogram or pulmonary function test results)
- To update and maintain subject screening and enrollment logs
- To monitor and report all adverse experiences and abnormal results to the Investigator, Sponsor and IRB if necessary
- Meet with the Sponsor's representatives to discuss the conduct of the study and review study data
- To obtain proper written informed consent from each study participant prior to participation in the study
- To recruit patients for participation in clinical research studies according to research ethics board recommendations
- To create & complete source documents and any other research documents required for the successful conduct of a clinical research study
- To be knowledgeable of the protocol so that all study activities are completed correctly
- Strong communication and interpersonal skills
- Registered in good standing as an RN with the College of Nurses of Ontario
- Proficiency with MS Office including creating spreadsheets, reports and presentation
- Previous experience with phlebotomy is an asset
- Strong knowledge of medical terminology
- Knowledge of general research procedures and regulatory requirements
- Detail oriented with exceptional organizational skills
- Education allowance (days and funding)
- Comprehensive Health Benefits
- Pension contribution matching
- Additional holiday closures
- Employee Appreciation days off
- Opportunities to work with internationally renowned Researchers & KOL’s
- 2019 All Star Site Challenge Winners (ACRP)
- Competitive Salary
- 2017 Clinical Researcher of the Year Award (CROY)
- Ongoing career training and development
- 2014 and 2015 Canada’s Best Workplaces™
- 2017 Site Patient & Recruitment Innovation Award (SPRIA) Winner
- 2016 Certified Best Workplace™
- State of the art Electronic Medical Records (EMR) environment
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