Data Coordinator (Clinical Trials)| NRL at Ampath

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.