PHARMAFull-time
Clinical Data Programmer II
By Admin · Clinical Data Management
INDIA (IN)HYBRIDPOSTED: 10/2/2026
PHARMAFull-time
HIRING ORGANIZATIONNOVOTECHBiosciences / Healthcare
ROLE OVERVIEW
Drive core clinical trial programming, database design, and data validation activities at a leading global CRO, ensuring strict compliance with GCDMP and ICH-GCP standards.
ROLE DEFINITION & RESPONSIBILITIES
- •Design, program, test, and maintain clinical trial databases across diverse EDC applications
- •Program data review listings, data reconciliation scripts, and external data load routines
- •Annotate CRFs according to CDISC standards and sponsor metadata specifications
- •Liaise with external laboratory and specialty vendors to define and implement data transfer specifications
- •Support computer system validation (CSV) and software verification under ICH-GCP and 21 CFR Part 11
- •Collaborate with cross-functional data management teams and participate in client project meetings
Reporting Hierarchy: Reports to Data Management Lead / Clinical Data Programming Manager • Team size: 10-15
* Role responsibilities and qualifications synthesized based on industry benchmark standards.
QUALIFICATIONS & REQUIREMENTS
REQUIRED QUALIFICATIONS
- Graduate in Information Science, Life Sciences, or related field
- Minimum 2 years of clinical data programming experience in a CRO or pharmaceutical setting
- Hands-on experience developing, testing, and maintaining clinical trial databases in EDC systems
- Strong working knowledge of GCDMP, ICH-GCP, and standard operating procedures (SOPs)
PREFERRED QUALIFICATIONS
- •Experience with CDISC SDTM metadata annotations and CRT specifications
- •Familiarity with SQL, SAS, or Python for clinical data review and reconciliation listings
- •Experience handling third-party external data streams such as Central Labs and ECGs
REQUIRED VERIFIED SKILLS
EDC Systems
Clinical Data Programming
GCDMP
ICH-GCP
Data Reconciliation
External Data Loads
CRF Annotation
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
Benefits: NovoLife flexible benefits framework, health insurance, paid parental leave for both parents, flexible leave entitlements, wellness programs, and continuous development initiatives.
Compensation for 2-5 years CDP professionals in India typically ranges from INR 6,00,000 to INR 11,00,000 annually depending on EDC technical certifications and CRO exposure.
ORGANIZATION CONTEXT & CULTURE
Novotech is a globally recognized full-service clinical Contract Research Organization (CRO) operating across Asia-Pacific, North America, and Europe.
TEAM SIZE: 1,001-5,000 employees
INDUSTRY: Biosciences / Healthcare
Culture: Values ambition, flexibility, and diversity through their NovoLife framework and is an accredited Employer of Choice for Gender Equality.
EXPECTED CAREER ROADMAP
Progression paths include Senior Clinical Data Programmer, Lead Data Programmer, and Technical Solutions Architect within global clinical operations.
APPLICATION ADVISORY
Highlight specific EDC platforms programmed (e.g., Medidata Rave, Veeva EDC) and mention familiarity with CDISC CRF annotation standards.
RECOMMENDED TRAINING
1/5
READY TO SUBMIT?
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