Clinical Data Specialist

15 hours ago


Solapur, Maharashtra, India beBeeQuality Full time ₹ 10,00,000 - ₹ 15,00,000

The role of a Central Monitor II is pivotal in ensuring the quality and integrity of clinical trial data.

Main Responsibilities
  • Develop Risk-Based Quality Management strategies to identify potential issues and improve overall data accuracy.
  • Conduct thorough study risk assessments and analyze statistical data to detect anomalies and trends.
  • Support monthly meetings with cross-functional teams to ensure data compliance and accuracy.
  • Collaborate with clinical operations, data management, and biostatistics departments to achieve shared goals.

This position requires a strong foundation in life sciences, statistics, or clinical operations.

Key Requirements
  • Bachelor's Degree in a relevant field.
  • At least 2 years of experience in clinical monitoring or clinical trial management.
  • Familiarity with ICH GCP guidelines and the clinical development process.

Prior experience as a Central Monitor in a Contract Research Organization (CRO) is advantageous.

Essential Skills
  • Proficiency in statistical analysis and data monitoring techniques.
  • Able to identify and mitigate risks associated with clinical trials.
  • Excellent report writing and presentation skills.

Precision Medicine Group is an equal opportunity employer.



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