Clinical Data Services Specialist – Clinical Data Operations | Bengaluru, India
Job ID: AIOC-S01628465
Location: Bengaluru, India
Job Type: Full-Time
Experience Required: 7–11 years (Clinical Data Management / Clinical Data Operations)
Qualification: Bachelor’s or Master’s Degree in Life Sciences
Job Overview
We are seeking an experienced Clinical Data Services Specialist to join a high-performing Life Sciences R&D team in Bengaluru. This role focuses on Clinical Data Operations and supports global biopharmaceutical clients in delivering accurate, compliant, and high-quality clinical trial data.
The ideal candidate will bring strong expertise in Clinical Data Management (CDM), vendor oversight, data transfer processes, regulatory compliance, and cross-functional collaboration within a global services environment. This position may require rotational shifts based on project requirements.
Key Responsibilities
Clinical Data Operations & Oversight
Provide technical solutions across functional areas including Vendor Qualification Assessment, Data Transfer Specification (DTS) creation, Test Data Review, Data Review Model development, Data Loading Monitoring, and LNMT setup.
Oversee clinical trial data collection, validation, reconciliation, storage, and analysis activities.
Ensure data integrity, quality control, and compliance with regulatory standards such as ICH-GCP and applicable global guidelines.
Clinical Study & Regulatory Support
Demonstrate strong understanding of clinical study management, clinical data workflows, and regulatory operations.
Support database build, data acquisition, and clinical reporting processes.
Monitor vendor deliverables and ensure timely resolution of data discrepancies.
Collaboration & Process Optimization
Collaborate with Data Acquisition Analysts and cross-functional stakeholders to develop and maintain a robust support model.
Drive issue resolution, corrective action tracking, and continuous improvement initiatives.
Share best practices across teams to enhance operational efficiency and quality standards.
Problem Solving & Leadership
Analyze and resolve moderately complex data management issues.
Develop new solutions by adapting existing methods and processes where required.
Manage small teams or workstreams, ensuring alignment with organizational objectives.
Build strong client relationships and support strategic initiatives defined by senior management.
Required Qualifications
Bachelor’s or Master’s Degree in Life Sciences.
7–11 years of experience in Clinical Data Management or Clinical Data Operations.
Strong knowledge of clinical trial processes, data management systems, and regulatory frameworks.
Experience working in global, matrix-based environments supporting pharmaceutical or biotech clients.
Key Skills & Competencies
Adaptability and flexibility in dynamic work environments.
Strong analytical and problem-solving skills.
Ability to perform effectively under pressure and tight timelines.
Client relationship management capability.
Agility and willingness to learn new technologies and methodologies.
Experience working in rotational shifts (as required).
Preferred Experience
Hands-on experience with vendor data management, data transfers, and database reconciliation.
Exposure to clinical reporting and regulatory submissions.
Leadership experience managing small teams or functional workstreams.
Why Apply Through ThePharmaDaily
This opportunity is ideal for experienced Clinical Data Management professionals seeking leadership exposure in Clinical Data Operations, vendor oversight, regulatory compliance, and global life sciences delivery models.
If you have strong expertise in clinical data services, regulatory frameworks, and cross-functional collaboration within pharmaceutical or biotech environments, apply now to advance your career in clinical data operations and life sciences R&D.
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