Clinical Data Coordinator - Flexible Hours & Growth

Medpace

Singapore

On-site

SGD 40,000 - 60,000

Full time

14 days+
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Benefits offered by this job

Flexible work environment
Competitive compensation and benefits package
Competitive PTO packages
Structured career paths with opportunities for professional growth
Company-sponsored employee appreciation events
Employee health and wellness initiatives

Job summary

Medpace is seeking a full-time Data Coordinator to join our Singapore team. You will play a vital role in ensuring the integrity of clinical data while maintaining study documentation and performing quality control audits.

The ideal candidate should have a Bachelor’s degree in a health-related field, along with strong attention to detail and relevant experience. This position offers opportunities for professional growth in a flexible work environment.

Join us and contribute to exciting clinical trials!

Qualifications

  • Strong attention to detail and proficiency in Excel and Word required.
  • 1-2 years of experience in a pharmaceutical or CRO setting preferred.
  • Knowledge of medical terminology is preferred.

Responsibilities

  • Track case report forms.
  • Clean and update the clinical database, including generating and resolving data clarifications.
  • Reconcile clinical data.
  • Maintain study documentation.
  • Perform QC audits of the clinical database.

Skills

Attention to detail
Knowledge of medical terminology
Working knowledge of Excel
Working knowledge of Word

Education

Bachelor's degree in a health-related field

Job description

Medpace is seeking a full-time Data Coordinator to join our Singapore team. You will play a vital role in ensuring the integrity of clinical data while maintaining study documentation and performing quality control audits.

The ideal candidate should have a Bachelor’s degree in a health-related field, along with strong attention to detail and relevant experience. This position offers opportunities for professional growth in a flexible work environment.

Join us and contribute to exciting clinical trials!

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