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%
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
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.








