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QACE Data Coordinator

DM Clinical Research
Cambridge, VT Remote Contractor
POSTED ON 8/4/2024 CLOSED ON 8/14/2024

What are the responsibilities and job description for the QACE Data Coordinator position at DM Clinical Research?

QACE Data Coordinator (Remote)

The Quality Assurance & Clinical Excellence Data Coordinator role is a critical position that requires the candidate to identify and investigate clinical related issues and trends which may impact study outcomes and/or study integrity.

DUTIES & RESPONSIBILITIES
  • Collect clinical data obtained from various sources to identify issues and anomalies that could impact a study’s overall quality.
  • Collaborate with teams, such as, QACE team, regulatory team, data team, clinical data, and other research staff to ensure all respective data is available.
  • Present findings to stakeholders and communicate corrective action plans.
  • Review study data and accurately capture all action items they contain, including but not limited to regular scheduled visits, sponsor audits, remote monitoring visits.
  • Investigate to see if Action Items by respective stakeholders, both internal and external, have been addressed by the site.
  • Apply clinical knowledge of checking to see if queries are addressed properly and communicate/escalate any issues that don’t have a satisfactory resolve.
  • Ensure the adherence to ALCOA , GDP, GCP Standards with all relevant clinical trial documentation.
  • Conduct review of source creation for clinical studies.
  • Add issues found on the query management system to keep a central repository of all items.
  • Identify trends and patterns which may have a potential impact on study outcomes and communicate to stakeholders in a clear and concise manner.
  • Assist in the training of new team members.
  • Submit required administrative paperwork per company timelines.
  • Any other matters, as assigned by management.

KNOWLEDGE & EXPERIENCE

Education:
  • Foreign Medical Graduate/PharmD/Clinical Research Professional/Advanced Degree in Health Science
Experience:
  • 1 years’ experience in a functional clinic setting, demonstrating ability to handle clinical problem-solving skills.
  • Experience with relevant regulations and guidelines (e.g., ICH-GCP, FDA regulations, ALCOA ) and experience working with clinical data management systems.
  • Experienced in spreadsheet software, Microsoft Excel, Google Sheets.
  • Experience in quality assurance and quality control in a clinical setting.
  • Experienced in auditing processes.
Knowledge and Skills:
  • Meticulous attention to details and deadlines.
  • Knowledge of basic use of scientific methods, procedures, and techniques.
  • Exceptional problem-solving skills, and root cause analysis of issues.
  • Ability to work independently and as part of a team.
  • Strong communication, organizational, and interpersonal skills.
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