Clinical Research Coordinator - Brampton, Canada - UPTOWN EYE SPECIALISTS

UPTOWN EYE SPECIALISTS
UPTOWN EYE SPECIALISTS
Verified Company
Brampton, Canada

2 weeks ago

Sophia Lee

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Sophia Lee

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Description

Clinical Research Coordinator

Job Summary:


  • Study regulatory approval tasks (REB, Health Canada etc)
  • Study administration tasks (patient interface, data collection, consent, data documentation as required by regulatory bodies etc)
  • Data management tasks (recording, analysis etc)
  • Project communication and team management

Responsibilities:


  • Overseeing the daily tasks, organization and clear communication to all research stakeholders and ensuring the sponsor is aware of the current status of their studies as well as resolved or ongoing protocol deviations.
  • Acts as a point of contact when study participant has questions and concerns are escalated, related to the clinical intervention being delivered in the study.
  • Responsible for oversight of study medical records, Providing timely study, updates/reports under supervision from the Principal Investigator.
  • Document all records of research activities and present to sponsors as per protocols.
  • Organize Daily/weekly/Monthly team meetings to ensure proper communication with all stakeholders.
  • Responsible for collaborating with the Investigator, Corporate Research Coordinator and other relevant partners involved in the project both internally and externally during the conduct of the research and knowledge translation.
  • Preparing and maintaining any study documents and materials as required.
  • Proactively identifies barriers/threats/risks for project completion and work with team members.
  • Coordinating study visits and collection of study data and materials.
  • Organizing and coordinating the involvement of other hospital departments/divisions related to new and/or ongoing studies.
  • Entering data, checking data for accuracy and completeness, including data reentry; data cleaning.
  • Use the log detailing activity to allocate the worked hours for each study project for financial and administration purposes

Job Requirements:


  • Undergraduate or Postgraduate background in healthcare research or related disciplines (eg. Public Health, Health Policy or related health policy field preferred)
  • Certified from the Association of Clinical Research Professionals ACRP certified or SOCRA.
  • Minimum of 02 years of clinical research experience in the sponsored research study experience in Canada.
  • Excellent written and verbal communication skills
  • Project management and organizational skills to manage multiple parallel processes
  • Proven ability to work independently, take direction from various sources and prioritize workload with particular attention to detail
  • Demonstrated organizational, communication, and interpersonal skills and ability to work within a fastpaced multidisciplinary team environment.

Salary:

$23 to $28/Hour


Job Status:

Full time, Regular


Timing:

8:00am to 4:00pm


Benefits:


  • Vision care
  • Dental care
  • Extended health care

Travel Requirements:

This job require travel to other sites.


Salary:

$23.00-$28.00 per hour


Benefits:


  • Dental care
  • Extended health care
  • Vision care

Schedule:

  • 8 hour shift
  • Monday to Friday

Supplemental pay types:

  • Bonus pay

COVID-19 considerations:
We are a medical facility. all employees are required to wear a mask, and must be fully vaccinated.


Ability to commute/relocate:

  • Brampton, ON: reliably commute or plan to relocate before starting work (preferred)

Experience:


  • Canadian: 1 year (required)
Healthcare Research: 2 years (required)


Licence/Certification:

  • ACRP or SOCRA Certification (required)

Work Location:
One location
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