Clinical Data Specialist
Bengaluru, India (Hybrid)
Also available in additional locations
Full-time
R1477949
The Clinical Data Specialist will provide comprehensive support and expertise in eCOA Data Management. This includes delivering quality data management solutions that meet customer needs, supporting operational data tasks, and collaborating closely with the eCOA Data Team Lead (DTL). The role may also involve task leadership in specific areas of large clinical trials.
Serve as Data Operations Coordinator (DOC) for multiple global clinical trials or lead a specific data management task.
Act as back-up for the Data Team Lead (DTL) or DOC with minimal guidance.
Lead specific eCOA or clinical data management tasks, including data reconciliation and monitoring.
Manage delivery of assigned projects through the full data management lifecycle.
Perform comprehensive quality control (QC) procedures across data management tasks.
Independently identify solutions and escalate issues to the eCOA DM team as needed.
Maintain effective communication and working relationships with eCOA DM teams and cross-functional project teams.
Negotiate timelines, responsibilities, and priorities with team members.
Participate in process improvement discussions and suggest innovative solutions.
Ensure compliance with core operating procedures (SOPs) and work instructions.
Assist with development and implementation of new technologies in the eCOA data management domain.
Meet all assigned objectives and timelines with minimal supervision.
| Requirement | Details |
|---|---|
| Education | Bachelor’s degree in Clinical, Biological, or Mathematical Sciences, or Nursing (Required) |
| Experience | Minimum 3 years of clinical trials experience in a role related to data management |
| Technical Skills | Working knowledge of SAS is a plus, but not required |
| Domain Knowledge | Thorough understanding of the data management process; knowledge of Medical Terminology, Pharmacology, Anatomy, and/or Physiology |
| Project Experience | Proven experience managing the full lifecycle of clinical data management in several large Phase I trials or at least one medium-sized Phase III trial |
| Soft Skills | Strong organizational, detail-oriented, and communication skills; ability to work independently and collaboratively; effective relationship management with teams, clients, and stakeholders |
IQVIA is a world leader in clinical research and healthcare analytics, offering services that support life sciences companies in accelerating drug development and improving patient outcomes. We empower customers through intelligent connections between data, technology, and expertise.
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