Clinical Data Specialist - Data QC & Regulatory Prep

IQVIA Inc; Centurion; On-site; ZAR 1,418,000 - 1,734,000; Full time

Job summary

IQVIA Inc in Centurion, South Africa is seeking a Clinical Data Specialist to provide basic and some advanced data management services within the CDM team. The role may include team leadership tasks under supervision.

Responsibilities include post-lock activities, quality control, regulatory submission preparation, and maintaining strong cross-functional communication with the global eArchiving team. The position is full-time and on-site.

Qualifications

• Bachelor’s degree in clinical, biological or mathematical sciences or related field required.
• Medical terminology exposure; strong organizational and communication skills.
• Ability to work independently and resolve problems with initiative.

Responsibilities

• Serve as a Clinical Data Specialist with guidance.
• Conduct post-lock activities (eArchiving, Hyperlinking).
• Perform comprehensive quality control procedures.
• File preparation for regulatory submission and site audits.
• Interact with team to negotiate timelines and responsibilities.
• May serve as back-up to SME or PLA Lead.

Skills

Organizational skills

Communication skills

Leadership

Computer skills

Education

Bachelor's Degree in Clinical/biological/mathematical sciences

Equivalent combination of education/experience in lieu of degree

Job description

IQVIA Inc in Centurion, South Africa is seeking a Clinical Data Specialist to provide basic and some advanced data management services within the CDM team. The role may include team leadership tasks under supervision.

Responsibilities include post-lock activities, quality control, regulatory submission preparation, and maintaining strong cross-functional communication with the global eArchiving team. The position is full-time and on-site.