Data Coordinator (Clinical Trials)| NRL
Ampath · Centurion, Gauteng
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Start free — we apply for you →What You Will Do
Provide Support and Data Accuracy
- Collect raw data from relevant testing laboratories for the verification, review, and archiving of patient and study data.
- Check and verify laboratory results to ensure accurate and timely reporting to clients and study stakeholders.
- Perform data capturing activities to maintain accurate and complete records.
- Review test runs, calculations, results, and reference ranges to ensure the correct setup and execution of clinical studies.
- Prepare source documentation and raw data for audits, ensuring records are readily available and compliant with quality requirements.
- Support internal and external audit processes by collaborating with the Total Quality Management TQM team and auditors.
- Build and maintain positive relationships with clients and stakeholders, promoting Ampath's professional reputation.
- Archive study documentation and raw data to ensure secure, compliant, and efficient storage and retrieval of information.
Provide Additional Administrative Support
- Assist with additional administrative tasks and ad hoc requests as required to support departmental objectives and ensure efficient workflow management.
What you'll bring
Qualifications
- Grade 12.
Advantageous
- Good Clinical Practice GCP, Good Laboratory Practice GLP, or Good Clinical Laboratory Practice GCLP certification.
- Medical Technician or Medical Technologist qualification.
Experience
Required
Minimum of 4 years' clinical trial or laboratory experience within a pathology environment, preferably supported by a medical technology background.
Knowledge & Skills
- Meticulous attention to detail with a strong commitment to data accuracy and quality.
- Strong interpersonal and communication skills, with the ability to collaborate effectively with clients, auditors, laboratories, and internal teams.
- Knowledge of Good Laboratory Practices and quality assurance processes.
- Sound understanding of regulatory requirements and Good Clinical Practice GCP standards.
- Strong analytical skills with the ability to identify trends, discrepancies, and inconsistencies in complex data sets.
- Exceptional organisational and document management skills.
- Ability to work independently while managing multiple priorities and deadlines.
- High level of professionalism and integrity when handling sensitive information.
- Exceptional discretion with sensitive information, maintaining strict confidentiality of records, study data, and stakeholder discussions at all times.