Senior Clinical Data Analyst

2 days ago

Palakkad, Kerala, India beBeeData Full time ₹ 80,00,000 - ₹ 1,20,00,000
Job Title:

Clinical Data Management Specialist

Job Description:

We are seeking a skilled Clinical Data Management Specialist to join our team. The ideal candidate will have a strong understanding of clinical trial data management, including protocol conversion, database build, CRF design, and data review and reconciliation tools.

  • Develop project specifications for Data Management services, including Protocol Conversion, Database Build, CRF Design, and Data Review and Reconciliation tools.
  • Understand external data collection, its integration into the clinical trial, and the management and reconciliation processes required to ensure its accuracy and relevance.
  • Execute data cleaning strategies to accelerate the time to achieve subject data cleanliness and ensure high-quality, timely deliverables.
  • Perform holistic data review and trending analysis via reporting and analytics to proactively identify issues, risks, and develop mitigation strategies.
  • Utilize artificial intelligence (AI) and machine learning (ML) for anomaly and outlier detection to enhance the efficiency and quality of trial data.
  • Monitor and interpret key performance indicators (KPIs), metrics, dashboards, Clinical Trial Operational Analytics (CTOA), and reports to provide actionable recommendations to study leads/project managers.
  • Perform query management tasks.
  • Define specifications and collaborate with technical teams on configuration of centralized data management platforms for data cleaning strategy and oversight activities.
  • Prepare and maintain data management documentation, such as DMPs, CCGs, help texts, and DVS.
  • Review and ensure the quality control of team-developed deliverables, including eCRFs, study documents, program/report specifications, outputs, and data central analytics modules.
  • Collaborate and work as a team to ensure deliverables are completed on time with high quality.
  • Ensure compliance with industry quality standards, regulations, guidelines, and procedures.
Requirements:
  • Strong knowledge of clinical trial data management principles, practices, and technologies.
  • Excellent communication and interpersonal skills.
  • Ability to work independently and collaboratively in a team environment.
  • Proven track record of delivering high-quality results under tight deadlines.
  • Proficiency in MS Office, particularly Excel, Word, and PowerPoint.
Benefits:

Our company offers a competitive salary and benefits package, including medical, dental, and vision insurance, 401(k) matching, paid time off, and professional development opportunities.

Other Information:

The ideal candidate will be flexible, adaptable, and able to prioritize multiple tasks and projects simultaneously. We are an equal opportunity employer and welcome applications from diverse candidates.

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