Clinical Data Specialist - Data Quality & Archiving

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

Job summary

IQVIA Inc is seeking a Clinical Data Specialist to provide data management support within the CDM team in South Africa. You will handle post-lock activities, maintain documentation, and ensure quality control while adhering to standard procedures.

The role involves collaborating with global teams, managing timelines, and preparing files for regulatory submissions and audits. Prior medical terminology exposure and strong communication skills are essential.

Qualifications

• Bachelor’s degree in clinical, biological or mathematical sciences or related field.
• Equivalent combination of education, training and experience in lieu of degree.
• Exposure to medical terminology; excellent organizational, communication, leadership and computer skills; attention to detail; ability to work independently and collaborate with coworkers and clients.

Responsibilities

• Provide data management expertise to the Clinical Data Management (CDM) team.
• Perform post-lock activities (eArchiving, Hyperlinking).
• Follow standard user manuals and working instructions; perform quality control procedures.
• Coordinate timelines and responsibilities with team members; interact with global eArchiving team and management.
• Prepare files for regulatory submission and site audits; may back-up SME or PLA Lead.

Skills

Medical terminology exposure

Organizational skills

Communication skills

Leadership

Attention to detail

Initiative

Team collaboration

Education

Bachelor's Degree Clinical, biological or mathematical sciences

Equivalent combination of education, training and experience

Job description

IQVIA Inc is seeking a Clinical Data Specialist to provide data management support within the CDM team in South Africa. You will handle post-lock activities, maintain documentation, and ensure quality control while adhering to standard procedures.

The role involves collaborating with global teams, managing timelines, and preparing files for regulatory submissions and audits. Prior medical terminology exposure and strong communication skills are essential.