Senior Clinical Data Analyst

12 hours ago

Bengaluru, Karnataka, India beBeeClinical Full time ₹ 1,50,00,000 - ₹ 2,00,00,000
Key Roles of Senior Clinical Monitor

The Senior Clinical Monitor plays a crucial role in ensuring the quality and integrity of clinical trial data through centralized monitoring activities, statistical data review, and proactive risk management.

As a senior-level professional, you will lead development of robust Quality Management Plans (QMPs) by collaborating with cross-functional teams to design and implement comprehensive plans tailored to each study's specific needs. Additionally, you will conduct thorough risk assessments for clinical studies, identifying potential issues and developing mitigation strategies.

  • Develop QMPs: Collaborate with cross-functional teams to create comprehensive QMPs that address each study's unique requirements.
  • Risk Assessment: Conduct thorough risk assessments for clinical studies to identify potential issues and develop effective mitigation strategies.

In this critical role, you will also perform centralized statistical monitoring & data analysis on study data to detect anomalies, trends, and potential risks. Moreover, you will lead facilitation of regular meetings by supporting review of study data, documenting findings, action plans, and coordination of data cleaning activities.

Essential Qualifications:
  • Bachelor's Degree in a relevant field such as life sciences, statistics, or data management.
  • Minimum 5 years experience in clinical monitoring or equivalent roles.
  • Working knowledge of ICH GCP guidelines and clinical development processes.

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