Remote Clinical Data Manager for Impactful Trials

Placements24

Pretoria

Hybrid

ZAR 700,000 - 1,000,000

Full time

11 days ago

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Benefits offered by this job

Health insurance
Retirement savings plan
Paid time off
Remote work flexibility

Job summary

Placements24 is seeking an experienced Remote Clinical Data Manager to join a globally distributed team. This fully remote role focuses on data integrity, CDMPs, and supporting clinical trial analysis across studies.

You will oversee EDC databases, data validation, and QA processes while collaborating with statisticians and investigators to ensure timely, accurate data delivery. A strong focus on regulatory compliance and proactive communication is essential.

Qualifications

  • Bachelor's degree in a scientific or medical field.
  • 6+ years of clinical data management experience in pharma/biotech.
  • Proficiency with EDC systems (Medidata Rave, Oracle Clinical, Veeva).

Responsibilities

  • Develop and implement Clinical Data Management Plans (CDMPs).
  • Oversee design and build of clinical databases using EDC systems.
  • Manage data entry, data cleaning, and query resolution for data accuracy.
  • Develop and maintain data management documentation and data transfer specs.
  • Perform quality control checks on clinical data and database consistency.
  • Collaborate with statistical programming teams for data analysis and reporting.
  • Ensure compliance with ICH-GCP guidelines and regulatory requirements.
  • Train site personnel on data management procedures.
  • Participate in database lock activities and archival processes.
  • Contribute to continuous improvement of data management processes and standards.

Skills

Analytical thinking
Communication
Independent work
Multi-project management

Education

Bachelor's degree in life sciences

Tools

Medidata Rave
Oracle Clinical
Veeva

Job description

Placements24 is seeking an experienced Remote Clinical Data Manager to join a globally distributed team. This fully remote role focuses on data integrity, CDMPs, and supporting clinical trial analysis across studies.

You will oversee EDC databases, data validation, and QA processes while collaborating with statisticians and investigators to ensure timely, accurate data delivery. A strong focus on regulatory compliance and proactive communication is essential.

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