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Clinical Data Coordinator

Role overview

Qualifications

  • Minimum of a one-to-two-year post-secondary certification in a relevant field
  • Minimum of one to three years of related work experience with ongoing training
  • Strong communication skills
  • Attention to detail and commitment to self-development

Responsibilities

  • Assist in clinical data management activities for assigned projects
  • Prepare essential DM documentation for trial stages
  • Perform data review and query generation
  • Ensure approved study documentation is maintained in the trial master files

Key facts

Other skills

  • Communication
  • Detail Oriented
  • Teamwork
  • Self-Motivation

About the company

Alimentiv logo

Alimentiv

Contract Research Organizations (CRO)

From 1986 to 2020 we operated as Robarts Clinical Trials and built a strong foundation in the medical research community. In 2020, we became Alimentiv but retained our commitment to clinical trials, medical imaging, and precision medicine for GI-related ailments.

Company details

Company typeSME
IndustryContract Research Organizations (CRO)
Company size201 - 500

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Job description

Job Title: Clinical Data Coordinator
 
Job Salary: $41,000 - $68,000 CAD
 
Job Location: London, Ontario (hybrid/remote)       
 
Reports To: Manager, Clinical Data Management Support
 
Department/Unit Name: Clinical Data Management
 
Role Summary: Responsible for assisting in carrying out basic clinical data management activities for assigned projects, ensuring focus on data integrity, validity, reliability in accordance with standard processes, the sponsor guidelines, industry best practices and regulatory standards. Support the department and company in achieving objectives and strategic goals.

Project Support
  • Assist in essential DM documentation preparation for various trial stages (i.e. start-up, maintenance and closeout)
  • Assist in basic database and edit check testing activities.
  • Perform data review and query generation.
  • Perform data entry where required.
  • Update database to correct errors.
  • Assist with generating SAS requests and reviewing report outputs
  • Assist with generating Data Transfers and reviewing transfer outputs
  • Assist in the completion of all activities necessary for the finalization and transfer of clinical database and relate project documentation to sponsor.
  • Ensure approved study documentation is maintained and properly stored in the trial master files.

  • Department Support
  • Contribute to the continuous improvement of Data Management and the wider organization through information sharing, training and education.
  • Promote and be an advocate of Data Management internally and externally.

  • Qualifications
  • Applicants should have a minimum of a one-to-two-year post-secondary certification in a relevant field of study, or a minimum of one to three years of related work experience with ongoing training. The successful candidate must exhibit the following skills: self-motivation with strong communication skills and a commitment to achieving positive results. Strong attention to detail and keenness to understand the importance of building collaborative relationships to achieve results. Ability to engage in continuous learning and self-development. Ability to continually foster teamwork. 
  • PHISHING SCAM WARNING: Alimentiv is aware of the continued increase of phishing scams, leveraging various methods of attack via email, text, voice and social media. Please note that Alimentiv only uses company email addresses, which contain β€œ@alimentiv.com”, to communicate with candidates via email. If you are contacted by someone about an open job at Alimentiv, please verify the domain of the sender’s email address and that they are asking you to apply on this website. If you believe you’ve been a victim of a phishing scam, please contact your local government cyber authority to report.
     
    *Accommodations are available for applicants with disabilities upon request throughout the recruitment lifecycle

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    Marcus Rivera

    Chief Revenue Officer

    m.rivera@company.com
    linkedin.com/in/marcusrivera
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