Principal Clinical Data Manager Opportunity at Veeda Lifesciences
About Veeda Lifesciences
Veeda Lifesciences is an innovative, tech-driven Contract Research Organization (CRO) with:
Global presence across 9+ countries
Specialization in clinical trials (Phase I-IV), preclinical research, and bioanalytical services
Cutting-edge AI-powered platforms like Querent™ for enhanced trial efficiency
Strong commitment to regulatory compliance (USFDA, ICH-GCP standards)
📍 Location: Ahmedabad, India
📅 Application Deadline: July 31, 2025
Position: Principal Clinical Data Manager
Key Responsibilities
Lead end-to-end data management operations for multiple clinical studies
Serve as primary liaison for sponsor communications on all data-related matters
Ensure 100% compliance with USFDA, ICH-GCP, and global data protection regulations
Oversee eCRF development, SAE reconciliation, and MedDRA/WHODD coding
Implement continuous process improvements in data management workflows
Provide strategic leadership to cross-functional clinical teams
Candidate Requirements
Education:
Essential: B.Sc/M.Sc in Statistics, Life Sciences, or related field
Preferred: Additional certifications in CDISC, GCP, or clinical data management
Experience:
6-8 years in clinical data management
CRO or pharmaceutical industry experience strongly preferred
Proven track record in leading data management teams
Technical Skills:
- Advanced proficiency in SAP, QMS (Deviation/CAPA)
- Expertise in CDISC standards implementation
- Comprehensive knowledge of clinical database systems
Soft Skills:
- Exceptional leadership and team management
- Strong cross-functional collaboration abilities
- Excellent problem-solving and analytical skills
Why Join Veeda Lifesciences?
🔹 Technology Leadership: Work with AI-powered Querent™ platform
🔹 Global Impact: Contribute to groundbreaking Phase I-IV clinical trials
🔹 Career Advancement: Clear path to senior leadership roles
🔹 Learning Culture: Regular training and development programs
🔹 Diverse Workforce: Inclusive environment fostering innovation
Application Process
How to Apply
📩 Email: mahendra.t3705@veedalifesciences.com
📝 Required Documents:
Updated professional resume/CV
Tailored cover letter highlighting:
Clinical data management experience
Regulatory compliance expertise
Leadership achievements
Relevant certifications (CDISC, GCP, etc.)
Application Deadline: July 31, 2025
Interview Preparation
- Review latest ICH-GCP guidelines and USFDA regulations
- Prepare examples of successful eCRF implementations
- Be ready to discuss challenges in clinical data management
- Research Veeda’s recent clinical trials and technologies
