Data Coordinator (Clinical Trials)| NRL

In brief

**Overview** This role is for a Data Coordinator in Clinical Trials at Ampath, focusing on supporting clinical studies within a pathology environment. The position involves ensuring the accuracy, integrity, and compliance of patient and study data, as well as providing administrative support to departmental objectives. **What you will do** * 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. * Assist with additional administrative tasks and ad hoc requests as required to support departmental objectives and ensure efficient workflow management. **Requirements (from the original advert)** * **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:** * 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. **Who should apply** This role is suitable for a detail-oriented professional with a minimum of 4 years' experience in clinical trial or laboratory work within a pathology setting, ideally with a medical technology background. The ideal candidate will possess strong analytical, organizational, and communication skills, with a deep understanding of data accuracy, quality assurance, GLP, GCP, and regulatory requirements. They should be capable of working independently, managing multiple priorities, and exercising exceptional discretion and professionalism when handling sensitive information. Candidates with GCP, GLP, or GCLP certification or a Medical Technician/Technologist qualification would be at an advantage. **Deadline** Not specified **Reference** Original posting: https://www.myjobmag.co.za/job/data-coordinator-clinical-trials-nrl-ampath Source: myjobmag

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At a glance

• At least 4 years of experience.

• Google Cloud
• Data entry

Extracted automatically from the advert; confirm requirements on the original listing.

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