Clinical Data Insights Expert

7 days ago

Belgaum, Karnataka, India beBeeClinicalDataManagement Full time ₹ 15,00,000 - ₹ 25,00,000

Job Title:

Clinical Data Management Professional

As a Clinical Data Management Specialist, you will play a pivotal role in ensuring the accuracy and quality of clinical trial data.

  • Define project specifications for Data Management services, including Protocol Conversion, Database Build, CRF Design, and Data Review and Data Reconciliation tools. This entails working closely with cross-functional teams to establish clear guidelines and protocols.
  • Understand external data collection, its integration into the clinical trial, and the management and reconciliation processes required to ensure accuracy and relevance. This involves analyzing complex data sets and developing strategies to address any discrepancies or issues that arise.
  • Execute data cleaning strategies to accelerate subject data cleanliness and ensure timely deliverables. This requires a strong understanding of data manipulation techniques and the ability to identify and resolve data inconsistencies.
  • Perform holistic data review and trending analysis via reporting and analytics to identify issues, risks, and develop mitigation strategies. This involves staying up-to-date with the latest industry trends and best practices to inform your approach.
  • Utilize AI and ML for anomaly and outlier detection to enhance efficiency and quality of trial data. This requires a solid understanding of machine learning algorithms and their application in real-world scenarios.
  • Monitor and interpret key performance indicators (KPIs), metrics, dashboards, and reports to provide actionable recommendations. This involves analyzing complex data sets and identifying areas for improvement.
  • Collaborate with technical teams to configure centralized data management platforms and define specifications. This requires strong communication skills and the ability to work effectively with cross-functional teams.
  • Prepare and maintain data management documentation and update throughout the trial lifecycle. This involves maintaining accurate records and ensuring compliance with regulatory requirements.
  • Review and ensure quality control of team-developed deliverables, covering eCRFs, study documents, and outputs. This requires a keen eye for detail and the ability to identify and address any errors or discrepancies.
  • Ensure compliance with industry quality standards, regulations, guidelines, and procedures. This involves staying up-to-date with the latest regulatory requirements and adapting your approach accordingly.

Requirements:

  • Strong understanding of clinical data management principles and practices
  • Excellent analytical and problem-solving skills
  • Ability to work effectively in a team environment
  • Strong communication and interpersonal skills
  • Proficiency in relevant software applications and technologies

Benefits:

  • Opportunity to work on high-profile clinical trials
  • Professional development and growth opportunities
  • Collaborative and dynamic work environment

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