PHARMAFull-time
Database Developer (Rave EDC)
By Admin · Clinical Data Management
BANGALORE (IN)HYBRIDPOSTED: 9/8/2026
PHARMAFull-time
HIRING ORGANIZATIONPREMIER RESEARCHContract Research Organization / Clinical Research
ROLE OVERVIEW
Build and maintain clinical databases using Rave EDC and support clinical data management activities for biotech, medtech, and specialty pharmaceutical studies.
ROLE DEFINITION & RESPONSIBILITIES
- •Create eCRFs according to finalized study protocols
- •create data-entry screens for paper studies
- •design build and test clinical databases according to SOPs
- •program field derivations edit checks and CDMS screen flows
- •collaborate with Data Management, Statisticians, Project Managers, and sponsors on data management plans
- •write procedures validation and data extraction programs
- •maintain annotated CRFs and Trial Master File documentation
- •perform system testing and assist with QC of deliverables
Reporting Hierarchy: Reports within the Clinical Data Sciences/Data Management organization; collaborates with Data Management project teams, Statisticians, Project Managers, sponsors, and other clinical research stakeholders; direct reporting line and team size are not specified
* Role responsibilities and qualifications synthesized based on industry benchmark standards.
QUALIFICATIONS & REQUIREMENTS
REQUIRED QUALIFICATIONS
- Bachelor's degree or equivalent, or 5 years of relevant clinical research/drug development/healthcare experience in lieu
- 4 years of clinical database development experience or proven experience across primary job functions
- understanding of database development processes, SOPs, and working guidelines
- knowledge of ICH/GCP regulations
- fluent written and verbal English and required local language skills
- strong communication, organization, multitasking, and customer-service skills
PREFERRED QUALIFICATIONS
- •Clinical trials support or pharmaceutical industry experience
- •knowledge of FDA guidance documents, EU directives, and ISO 14155
- •understanding of drug/device development and clinical monitoring procedures
- •experience with web-based communication tools
- •experience maintaining CDMS global or program libraries
REQUIRED VERIFIED SKILLS
Rave EDC
clinical database development
eCRF design
CDMS
data management
SQL/programming
edit checks
data derivations
validation
quality control
ICH/GCP
documentation
communication
time management
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
Benefits: Competitive compensation; flexibility and work-life balance; professional growth and development opportunities; employee-focused workplace
No numerical salary range is disclosed. The posting indicates competitive compensation, so exact pay should be confirmed with Premier Research during recruitment.
ORGANIZATION CONTEXT & CULTURE
Premier Research is a global contract research organization supporting biotech, medtech, and specialty pharmaceutical companies in developing medicines, devices, and diagnostics.
TEAM SIZE: Global organization; employee count not stated in the supplied posting
INDUSTRY: Contract Research Organization / Clinical Research
Culture: Collaborative, flexible, inclusive, and growth-oriented culture emphasizing employee voice, accountability, innovation, work-life balance, and patient-focused medical research.
EXPECTED CAREER ROADMAP
The role provides a pathway into senior clinical database developer, lead database programmer, clinical data management, or broader clinical data sciences roles, with exposure to global clinical trials and sponsor-facing projects.
APPLICATION ADVISORY
Emphasize Rave EDC experience, clinical database builds, eCRF programming, edit checks, derivations, validation, SQL/programming, ICH/GCP knowledge, and experience supporting clinical trials. Highlight collaboration with sponsors and cross-functional clinical data teams.
RECOMMENDED TRAINING
1/5
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