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DC

QACE Data Coordinator I (4260)

DM CLINICAL RESEARCH GROUP
🇵🇰 Pakistan
On-site
4 weeks ago
  • GCP
  • PharmD
  • ICH-GCP
  • Excel
  • Google Sheets
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The QACE Data Coordinator I 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 research data obtained from various sources to identify issues and inconsistencies that could impact a study’s overall quality.
  • Collaborate with teams, such as the regulatory, clinical data, and research site teams, to ensure all respective data is available.
  • Review study data and accurately capture all action items, including those arising from scheduled site visits, sponsor audits, and remote monitoring.
  • Communicate/escalate any issues that don’t have a satisfactory resolution
  • Ensure the adherence to ALCOA+, GDP, GCP Standards, and FDA regulations with all relevant clinical trial documentation.
  • Conduct review of source creation for clinical studies against applicable documents, such as, the study protocol, lab manual, and pharmacy manual.
  • 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.
  • 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+).
  • Experience with working with clinical data management systems and auditing processes.
  • Experience in quality assurance and quality control in a clinical setting.

Credentials:

  •  N/A

Knowledge and Skills:

  • Meticulous attention to details and deadlines.
  • Knowledge 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.
  • Proficiency in spreadsheet software (e.g., Microsoft Excel, Google Sheets).

KPI & Success Metrics

  • Average minimum number of chart reviews per day= 5 per day
  • Valid findings review percentage= 85%
  • Paycom training completion by deadline= 95%
  • Successful Priority task completion by deadline= 95%

QACE Data Coordinator I (4260) · DM CLINICAL RESEARCH GROUP

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