LMC Manna Research is the largest network of fully-owned and integrated clinical research sites in Canada and one of the founding members of hyperCORE International.
We provide Phase I-IV clinical trial services with specialized focuses on endocrine disorders, real world evidence big data research, vaccine research, and primary care studies.
LMC Manna Research provides Sponsors, CRO’s & ARO’s access to one of the largest fully owned and operated clinical research site networks within Canada at 20 sites across 3 provinces.
Our mission is to improve the health of Canadians today and tomorrow through clinical research.
Currently, our rapidly expanding team and site network is looking for a Clinical Research Coordinator who can work for us on a full-time, permanent basis , supporting our LMC Ottawa and Manna Ottawa locations.
Responsibilities will include but are not limited to :
To conduct the clinical research study according to the study protocol, GCP, and the LMC Manna Research SOP / WP
To be knowledgeable of the protocol so that all study activities are completed correctly
To recruit patients for participation in clinical research studies according to research ethics board recommendations
To obtain proper written informed consent from each study participant prior to participation in the study
To screen the potential study participants according to the protocol’s inclusion and exclusion criteria
To schedule study participant visits as per protocol
To perform delegated protocol specific activities completely and accurately
To obtain vital signs as required per protocol (i.e. blood pressure, temperature, heart rate, waist measurement, weight & height)
To perform blood & urine collection, processing and shipping, as well as other on-site patient testing as needed (e.g. ECG)
Provide lifestyle adherence counseling & general training / education to study participants, as required by protocol
To obtain all necessary documentation as required by the protocol (i.e. ECG, echocardiogram or pulmonary function test results)
To monitor and report all adverse experiences and abnormal results to the Investigator, Sponsor and IRB if necessary
To update and maintain subject screening and enrollment logs
To create & complete source documents and any other research documents required for the successful conduct of a clinical research study
Meet with the Sponsor's representatives to discuss the conduct of the study and review study data
Bachelor of Science degree or related degree
Masters or post graduate diploma in Science is an asset
RN, RPN, or MLT an asset
A minimum of 1-2 years clinical research experience or equivalent certification
Recruitment experience is an asset
Strong attention to detail
Strong knowledge of medical terminology
Knowledge of general research procedures and regulatory requirements
Strong communication and interpersonal skills
Detail oriented with exceptional organizational skills
Proficiency with MS Office including creating spreadsheets, reports and presentation
LMC Manna Research seeks dynamic individuals who embrace learning and innovative opportunities and those who contribute to improving the health of Canadians today and tomorrow through clinical research.
Why LMC Manna might be right for you!
2019 All Star Site Challenge Winners (ACRP)
2017 Site Patient & Recruitment Innovation Award (SPRIA) Winner
2017 Clinical Researcher of the Year Award (CROY)
2016 Certified Best Workplace™
2014 and 2015 Canada’s Best Workplaces™
Comprehensive Health Benefits
Pension contribution matching
Education allowance (days and funding)
Ongoing career training and development
Employee Appreciation days off
Additional holiday closures
Opportunities to work with internationally renowned Researchers & KOL’s
State of the art Electronic Medical Records (EMR) environment
LMC Manna Research is committed to meet the accessibility needs of persons with disabilities in a timely manner. These accommodations will be available upon request.
We thank all candidates for their applications, however, only those candidates selected for an interview will be contacted