Clinical Research Coordinator - Toronto, Canada - TORONTO MEMORY PROGRAM

TORONTO MEMORY PROGRAM
TORONTO MEMORY PROGRAM
Verified Company
Toronto, Canada

3 weeks ago

Sophia Lee

Posted by:

Sophia Lee

beBee Recruiter


Description

The Company


Toronto Memory Program, a Headlands Research site, is Canada's largest and most experienced site for drug treatment trials in Alzheimer's disease and related conditions.

Founded in 1996, we have made significant contributions to over 100 drug treatment studies in Alzheimer's disease. Our Medical Director, Dr.

Sharon Cohen, a Canadian-trained behavioural neurologist, along with her team of highly trained research staff, have been committed to the development of better treatments for dementia for the past 18 years.


The Role
Toronto Memory Program, a Headlands Research site is looking for a Clinical Research Coordinator to manage clinical research protocols.

This individual will work directly with the investigators, patients and other research staff to ensure protocol visits are being conducted according to ICH GCP guidelines.


  • Strong organizational skills
  • Attention to detail
  • Passionate about making a different in patients' lives

Duties

  • Comprehend study design of each protocol that is assigned
  • Perform procedures in compliance with the study protocol
  • Collect and record study data in source documents via electronic system (CRIO)
  • Manage study related activities
  • Adherence to protocol requirements
  • Review laboratory data
  • Assess and document compliance
  • Manage investigational product
  • Assess, record, and report Adverse Events as outlined in the protocol
  • Manage/train ancillary staff

Qualifications

Education:


  • Experience and training in conducting clinical trials with knowledge of ICH GCP OR Two years of college in a healthrelated program or LPN/LVN OR Bachelor's degree in a health or scientific related program
  • A thorough understanding of regulatory requirements
  • Excellent interpersonal and communication skills
  • Experience performing clinical assessments, including but not limited to obtaining vital signs, EKGs, blood draws, processing/shipping lab specimens
  • Experience with CRIO (Clinical Trial Management System) is a plus
  • Experience with administering vaccines is a plus
At Headlands Research, we are building the best clinical trial company in the world.

We're an exceptional family of next-generation clinical trial sites, integrating cutting edge technology and high-quality support services, and significantly expanding participant outreach and participation.

Founded in 2018, our company is in high growth mode; we operate 15 clinical trial sites in the US and Canada and have rapid expansion plans


Job Types:
Full-time, Permanent


Benefits:


  • Dental care
  • Extended health care
  • Paid time off
  • Vision care

Schedule:

  • 8 hour shift
  • Monday to Friday

COVID-19 considerations:
Our company does have a mandatory COVID-19 vaccination policy for all employees.


Application question(s):

  • Our company has a mandatory COVID19 vaccination policy. Are you willing / able to comply with this policy?
  • What are your salary requirements?
  • This position is onsite (not remote) at our offices in the North York area. Is this commute possible and is this a comfortable commute for you?

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