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Clinical Data Coordinator

Key Facts

Remote From: 
Full time
Expert & Leadership (>10 years)
41 - 68K yearly
Italian

Other Skills

  • Collaboration
  • Communication
  • Teamwork
  • Training And Development
  • Results Focused
  • Detail Oriented
  • Lifelong Learning
  • Self-Motivation

Roles & Responsibilities

  • One-to-two-year post-secondary certification in a relevant field of study, or one-to-three years of related work experience with ongoing training.
  • Self-motivation with strong communication skills and a commitment to achieving positive results.
  • Strong attention to detail and ability to build collaborative relationships to achieve results.
  • Ability to engage in continuous learning, self-development, and foster teamwork.

Requirements:

  • Assist in essential data management documentation for trial stages (start-up, maintenance, closeout) to support data integrity and regulatory compliance.
  • Perform data review and edit check testing; generate and resolve data queries; update the database to correct errors.
  • Assist with generating SAS requests, reviewing report outputs, and facilitating Data Transfers and transfer outputs to sponsor.
  • Support data management department goals by contributing to continuous improvement, information sharing, training, and advocacy internally and externally.

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 “@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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