Clinical Data Specialist – Clinical Data Management | EDC | Regulatory Compliance
Job ID: 576501
Location: Bangalore, India
Employment Type: Full-Time
Work Model: Office-Based (Minimum 3 Days In-Office Per Week)
Experience Required: 5–8 Years in Clinical Data Management
About the Company
Philips is a global health technology leader committed to improving lives through meaningful innovation. With a strong focus on accessible and quality healthcare, Philips delivers advanced solutions across clinical research, diagnostics, and medical technologies worldwide.
Role Overview
The Clinical Data Specialist is responsible for managing and supporting end-to-end clinical data management activities across pharmaceutical and medical technology projects. This role collaborates with cross-functional teams to implement technical data solutions, configure Electronic Data Capture (EDC) systems, and ensure compliance with global regulatory standards.
The position requires strong expertise in clinical database management systems, data quality assurance, and regulatory-compliant documentation practices within the pharma or medtech industry.
Key Responsibilities
Collaborate with cross-functional teams to configure and implement EDC systems and clinical programming solutions.
Ensure adherence to clinical data management standards, regulatory requirements, and internal SOPs.
Develop and maintain documentation, including SOPs and work instructions for data management processes.
Execute data processing activities while ensuring accuracy, consistency, and integrity of clinical datasets.
Support preparation of clinical data outputs including tables, listings, graphs, and summaries for analysis and reporting.
Evaluate data quality, completeness, and suitability for statistical analysis.
Identify discrepancies and anomalies, troubleshoot issues, and escalate complex technical challenges appropriately.
Coordinate with biostatistics and statistical programming teams for data transfer and integration.
Provide guidance and knowledge sharing to team members on data management best practices.
Required Qualifications
Bachelor’s Degree in Medical, Life Sciences, Pharmacy, Biotechnology, or related field (Mandatory).
5–8 years of experience in Clinical Data Management within the pharmaceutical or medical device industry.
Strong experience with Electronic Data Capture (EDC) systems.
In-depth understanding of regulatory compliance requirements in clinical research.
Experience in clinical database management systems and data harmonization processes.
Preferred Qualifications
Certification such as CCDM (Certified Clinical Data Manager) is an advantage.
Hands-on experience with Medidata Rave and Greenlight Guru platforms.
Strong knowledge of statistical methods and clinical reporting standards.
Experience in both Pharma and Medtech clinical environments.
Core Competencies
Clinical Data Management lifecycle expertise
Regulatory compliance and documentation
Data quality assurance and validation
EDC configuration and troubleshooting
Business intelligence and reporting tools
Cross-functional collaboration
Analytical thinking and problem resolution
Why Join Philips
Work with a globally recognized health technology innovator
Contribute to impactful clinical research initiatives
Collaborative office-based work model with structured team engagement
Competitive compensation and career development opportunities
Purpose-driven organizational culture focused on improving global healthcare access
Equal Opportunity Statement
Philips encourages applications from diverse backgrounds and is committed to creating an inclusive workplace environment.
This Clinical Data Specialist opportunity is ideal for experienced clinical data professionals seeking to advance their careers in EDC systems management, regulatory-compliant clinical data operations, and cross-functional clinical research collaboration within a global health technology organization.
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