Clinical Data Coordinator

OpenKrill; United States; Remoto; USD 29.000 - 48.000; Tempo pieno

Descrizione del lavoro

OpenKrill is seeking a Clinical Data Coordinator to assist in essential data management activities across clinical trials, ensuring data integrity and adherence to sponsor guidelines and regulatory standards.

You will support the Clinical Data Management team with documentation, database updates, edit checks, data review, and data entry as needed, contributing to the reliability and quality of trial data.

Competenze

• One-to-two years post-secondary certification or one to three years related work experience with ongoing training.
• Strong communication skills and self-motivation to achieve positive results.
• Attention to detail and ability to build collaborative relationships for results.
• Ability to learn continuously and work in a team environment.

Mansioni

• Assist in essential DM documentation for trial stages (start-up, maintenance, closeout).
• Assist in basic database and edit check testing activities.
• Perform data review and query generation.
• Perform data entry where required and update database to correct errors.
• Assist with SAS requests and reviewing report outputs.

Conoscenze

Communication skills

Self-motivation

Team player

Formazione

Post-secondary certification

Strumenti

SAS

Descrizione del lavoro

Job Title: Clinical Data Coordinator

Job Salary: $41,000 - $68,000 CAD

Reports To: Team Lead, Clinical Data Management

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.

Accommodations are available for applicants with disabilities upon request throughout the recruitment lifecycle