QACE Data Coordinator I (4260)

Posted 10 Days Ago
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Karachi, Sindh, PAK
In-Office
Junior
Healthtech • Professional Services • Biotech • Pharmaceutical
The Role
Collects and reviews clinical research data to identify inconsistencies, quality issues, and trends affecting study outcomes. Coordinates with regulatory, clinical data, and research site teams; documents action items from site visits, audits, and monitoring; escalates unresolved issues; and maintains query repositories. Ensures compliance with ALCOA+, GDP, GCP, and FDA requirements, reviews clinical source documents, performs root cause analysis, and completes administrative and priority tasks within deadlines.
Summary Generated by Built In

The QACE 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 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%

Skills Required

  • Foreign Medical Graduate, PharmD, Clinical Research Professional, or advanced degree in Health Science
  • At least 1 year of experience in a functional clinical setting
  • Experience with ICH-GCP, FDA regulations, ALCOA+, or similar clinical research regulations and guidelines
  • Experience with clinical data management systems and auditing processes
  • Experience in quality assurance and quality control in a clinical setting
  • Proficiency with spreadsheet software such as Microsoft Excel or Google Sheets
  • Meticulous attention to detail and deadlines
  • Knowledge of scientific methods, procedures, and techniques
  • Strong problem-solving and root cause analysis skills
  • Ability to work independently and as part of a team
  • Strong communication, organizational, and interpersonal skills
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The Company
700 Employees
Year Founded: 2006

What We Do

DM Clinical Research is a multi-therapeutic network of clinical trial investigator sites headquartered in Houston, Texas. Founded in 2006, the company connects patients with trusted physicians to conduct cutting-edge research focused on quality and compassion, aiming to deliver advanced, preventative medicine to underserved communities. They operate a national network of dedicated research centers and physician-embedded sites throughout the United States.

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