Rpn - Clinical Research Coordinator - London, Canada - Centricity Research

Centricity Research

Verified Company

London, Canada

2 weeks ago

Posted by:

Sophia Lee

beBee Recruiter

Description

Aventiv Research, IACT Health, LMC Manna Research, and True North Clinical Research have united to become the largest network of fully-owned and integrated clinical research sites in North America, Centricity Research.

The sites that were formerly known as Aventiv operating in Ohio and Arizona and specialize in phase 1 pharmaceutical, device, and diagnostic clinical trials in a variety of therapeutic areas throughout phases 1-4.

The sites that were formerly known as IACT Health brings phase I-IV clinical trials in over 30 therapeutic areas such as oncology, cardiology, pulmonology, endocrinology, infectious disease, and pain with wholly owned and integrated clinical research offices in multiple cities in the United States across the Southeast, including Georgia and Virginia.

The sites that were formerly known as LMC Manna bring phase I-IV clinical trial services with specialized focuses on endocrine disorders, real world evidence big data research, vaccine research, and primary care studies within Canada at sites across Alberta, Ontario, and Quebec.

The sites that were formerly known as True North Clinical Research are located in Nova Scotia and specialize in research related to Alzheimer's disease and conditions related to aging, and are committed to finding new treatments to maintain an improved quality of life for patients through innovation and passion.

Currently, our rapidly expanding team and site network is looking for a
Registered Practical Nurse (RPN) Clinical Research Coordinator who can work for us on a
full-time permanent, supporting our
London location.

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 onsite patient testing as needed (e.g. ECG, pulmonary function testing, IV infusion)
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 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

Requirements:

Diploma in nursing
Registered in good standing as an RPN with the College of Nurses of Ontario
IV skills an asset
Previous experience with phlebotomy is an asset
Knowledge of general research procedures and regulatory requirement is an asset
Strong communication and interpersonal skills required
Detail oriented with exceptional organizational skills required
Proficiency with MS Office including creating spreadsheets, reports and presentation is a strong asset

Centricity Research is committed to meet the accessibility needs of persons with disabilities in a timely manner. These accommodations will be available upon request.

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