PHARMAFull-time
CDM Programmer II
BANGALORE (IN)ONSITEPOSTED: 8/14/2026
PHARMAFull-time
HIRING ORGANIZATIONTHERMO FISHER SCIENTIFICLife Sciences / Scientific Instruments / Biotechnology
ROLE DEFINITION & RESPONSIBILITIES
Design, build, and test clinical trial databases and edit checks in Veeva EDC.
Manage Post-Production Changes (PPCs) and perform Retrospective Amendments and CDB programming tasks.
Define, import, and validate clinical trial data across systems while creating listings for data review.
Act as lead programmer on simple to moderately complex clinical studies under supervision.
Adhere to GCPs and departmental SOPs while participating in continuous process improvement initiatives.
REQUIRED VERIFIED SKILLS
Veeva EDC
CDM Programming
Edit Checks
Post-Production Changes (PPC)
CDB Programming
SQL
SAS
Data Validation
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
ORGANIZATION CONTEXT & CULTURE
Thermo Fisher Scientific is a global leader in serving science, providing an extensive range of analytical instruments, laboratory equipment, reagents, consumables, software, and services. They partner with pharmaceutical and biotech companies, hospitals, clinical diagnostic labs, universities, research institutions, and government agencies. The company's mission is to enable its customers to make the world healthier, cleaner, and safer.
TEAM SIZE: 130,000+ employees
INDUSTRY: Life Sciences / Scientific Instruments / Biotechnology
RECOMMENDED TRAINING
1/4
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