Maiora is hiring skilled professionals for Lead Data Manager, Clinical Programmer, and Operational Specialist roles. These roles offer excellent growth opportunities in clinical data management, programming, and pharmacovigilance operations. If you have the required experience and are ready for your next career move, this is the perfect opportunity.
1. Lead Data Manager (Remote)
Experience: 6+ Years
Openings: 3
Location: Remote
Job Overview
Maiora is seeking an experienced Lead Data Manager with hands-on expertise in end-to-end clinical data management (CDM) using Veeva. Experience in study leadership and coding is a strong advantage.
Key Responsibilities
- Lead full-cycle Data Management activities: setup, conduct, and close-out
- Oversee CRF design, data validation, and database management in Veeva
- Manage cross-functional communication with clinical teams
- Review and troubleshoot data queries
- Provide technical oversight on CDM standards, quality, and timelines
Required Qualifications
- Minimum 6+ years of CDM experience
- Strong Veeva hands-on experience
- 2โ3 years of study leadership
- Coding knowledge preferred
- Excellent communication & documentation skills
2. Clinical Programmer (Remote)
Experience: 3โ6 Years
Openings: 4
Location: Remote
Job Overview
Maiora is looking for a skilled Clinical Programmer experienced in Veeva forms design, edit checks, TSDV setup, coding configuration, and migrations.
Key Responsibilities
- Build and customize forms and dynamics in Veeva
- Develop and validate edit checks/rules
- Support TSDV, coding setup, and post-production changes
- Manage CRF updates, versioning, and system migrations
- Collaborate with Data Management and Clinical teams
Required Qualifications
- 3โ6 years of clinical programming experience
- Strong Veeva programming workflow knowledge
- Experience in study build, rules, and operational setup
- Ability to troubleshoot and optimize EDC processes
3. Operational Specialist โ Pharmacovigilance
Experience: 1.5+ Years
Location: Bangalore / Thane
Job Overview
Maiora is hiring Operational Specialists for ICSR case processing and regulatory submission activities.
Key Responsibilities
- Process ICSR safety cases in safety databases
- Perform regulatory submissions as per SOPs & guidelines
- Track & review incoming AE/endpoint information
- Update case status, enter data, and perform coding
- Write safety narratives and support literature monitoring
Required Qualifications
- 1.5+ years of experience in pharmacovigilance
- Strong knowledge of global PV regulations
- Experience in ICSR processing, MedDRA coding & narrative writing
- Excellent analytical and documentation skills
Why Join Maiora?
- Work on global clinical research projects
- Opportunity to work remotely (for select roles)
- Exposure to advanced Veeva-based workflows
- Competitive salary package
- Professional development & internal growth opportunities
How to Apply
Eligible and interested candidates may send their resume to:
๐ฉ madhav.mantur@maiora.co
Subject Line: Application โ [Role Name]