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Protocol Intelligence
Data-driven signals on your job's competitivenessSpecialized senior clinical data programming role at a strong pharma brand in Bangalore yields moderate competition.
Role requires niche clinical trial, regulatory, and standards expertise, limiting cross-industry transferability.
Explicit 7+ years, domain certifications, and regulatory validation requirements make shortlisting highly strict.
Job Description
Structured overview of role & requirementsAbout This Role
Program and test clinical trial data collection databases ensuring accuracy, efficiency, and alignment with study objectives for trials or trial programs.
Partner with Clinical Data Management to deliver study databases ahead of first patient visit and support submission, inspection, and regulatory response activities.
Improve processes to reduce study build cycle time, enhance reusability of forms and edits, and reduce post-production changes through change control.
Minimum Requirements
At least 7 years of database programming and system validation experience in clinical, pharmaceutical, biotech, CRO or regulatory sectors.
Bachelor's degree in computer science, engineering, medical field, Informatics, Life Sciences, Health Information Administration, Statistics, IT, Nursing, or Pharmacy.
Job location: Bangalore, India.
Work Experience Required: Minimum 7 years database programming and system validation experience as detailed above.
Ideal Candidate Profile
Possesses strong therapeutic and scientific knowledge pertinent to clinical research and drug development.
Experience with clinical data tools and technologies, data standards, and eCOA data design/handling.
Demonstrated skills in project management, vendor management, and ability to liaise effectively with cross-functional study teams including Data Sciences, Statistics, PK, and Operations.