Hybrid Clinical Data Manager — Drive Trial Integrity

Placements24

Polokwane

Hybrid

ZAR 600,000 - 900,000

Full time

11 days ago
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Benefits offered by this job

Hybrid work model
Medical insurance
Professional development

Job summary

Placements24 is seeking a skilled Clinical Data Manager to join the team in Polokwane in a hybrid role. You will manage and ensure the integrity of clinical trial data across study databases, collaborating with clinical operations, biostatistics, and programming teams to deliver high-quality data for reliable evaluation of pharmaceutical products.

The role requires a Bachelor's degree in a relevant field and at least 4 years' experience in clinical data management within pharma/CRO settings,

Qualifications

  • Bachelor's degree in a relevant scientific or technical field.
  • Minimum of 4 years of experience in clinical data management within the pharmaceutical or CRO industry.
  • Proficiency with Electronic Data Capture (EDC) systems (e.g., Medidata Rave, Oracle Clinical).
  • Strong understanding of clinical trial processes, ICH-GCP, and data standards (e.g., CDISC).
  • Excellent analytical, problem-solving, and communication skills.
  • Ability to work effectively in a team environment and manage multiple projects simultaneously.

Responsibilities

  • Design, develop, and validate clinical databases using EDC systems.
  • Develop data management plans (DMPs) and data validation plans (DVPs).
  • Oversee data entry, data cleaning, query management, and database lock processes.
  • Ensure compliance with ICH-GCP guidelines and regulatory requirements for data management.
  • Collaborate with clinical teams to ensure consistency between protocols, CRFs, and databases.
  • Generate data management reports and provide status updates to project teams.

Skills

Analytical
Problem-solving
Communication
Team collaboration

Education

Bachelor's degree in a relevant field

Tools

Medidata Rave
Oracle Clinical

Job description

Placements24 is seeking a skilled Clinical Data Manager to join the team in Polokwane in a hybrid role. You will manage and ensure the integrity of clinical trial data across study databases, collaborating with clinical operations, biostatistics, and programming teams to deliver high-quality data for reliable evaluation of pharmaceutical products.

The role requires a Bachelor's degree in a relevant field and at least 4 years' experience in clinical data management within pharma/CRO settings,

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