GSK India
Senior Analyst, Data Acquisition
Skills
2 months ago
Share this opportunity
Share this opportunity to other talents of your network:
✓ Offer them a visibility boost with clients.
✓ Help your contacts find their next job.
Important information
Contract type:
Permanent
Location:
Bengaluru, Karnataka, India
Work mode:
Onsite
Published on:
2 September 2026
What they need
Job Summary
You will design, build and validate clinical data acquisition solutions. You will work closely with clinical operations, statistics, IT and external vendors to ensure high quality and compliant data for studies. We value clear communication, technical curiosity and continuous improvement. This role offers growth, real impact and the chance to help unite science, technology and talent to get ahead of disease together.
Responsibilities
- Design, develop, validate, and maintain complex clinical data review solutions and reporting assets.
- Lead implementation of CDB Checks, Listings, Reconciliations, Medical/Safety Reviews, PD Reviews, and CDMS reporting solutions.
- Translate protocol and business requirements into scalable, automated review workflows and visualizations.
- Provide technical oversight for solution architecture, coding standards, validation practices, and quality compliance.
- Develop reusable libraries, frameworks, and automation capabilities to improve efficiency and standardization.
- Support complex data reconciliations across EDC, laboratory, safety, imaging, and other external data sources.
- Mentor and provide technical guidance to programmers and study teams.
- Partner with Data Management and cross-functional stakeholders to deliver study milestones and inspection-ready outputs.
- Drive continuous improvement, innovation, and adoption of emerging technologies within clinical data review programming.
Basic Qualifications
- Advanced experience in Clinical Data Management, Clinical Data Review Programming, or related clinical systems roles.
- Strong expertise in Veeva CDB, Veeva CDMS Reports, Domino, R, Python, SQL, and clinical data standards.
- Deep understanding of clinical trial processes, data review methodologies, reconciliation processes, and regulatory requirements.
- Demonstrated ability to lead complex technical initiatives and influence cross-functional stakeholders.
Skills
- Clinical Trial Designs
- Python
- R Programming
- Veeva
Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.
Other offers great for you!
These companies are also looking for great profiles
Nexiqon
Chef de projet MOE Data Senior – Banque / Finance & Risques (H/F)
Permanent contract
Paris, France
Hybrid
Skills
13 hours ago
Quick apply
Anderson RH
Data Translation / Product Owner Senior- Retail
Freelance
Paris, France
Hybrid
Skills
11 hours ago
Quick apply
Anderson RH
Business Data Analyst Market Access
255 € HT/jour
Freelance
Remote
Skills
11 hours ago
Quick apply