Clinical Data Management 3-5Yrs

Key Responsibilities:

Build & configure Medidata Rave studies - CRF design, edit checks, derivations, and study deployments

Develop Custom Functions and edit check logic aligned to protocol and CDISC/CDASH standards

Good understanding of external data source integrations labs, IRT, ePRO into EDC and downstream workflows

Drive UAT and ensure all builds are audit-ready and compliant

Collaborate with Data Managers, eCRF Designers, Data Standards, Medical and Safety across the study lifecycle

Support Program in SAS, R, or Python to support data extraction, listings, and ad hoc analysis

Qualifications:

3-5 years of hands-on experience in Clinical Data Management or EDC programming

Strong proficiency in Medidata Rave study builds, ALS, edit checks, custom functions

Solid understanding of CDISC CDASH, GCP, and regulatory compliance

Experience with UAT, Data Validation Plan (DVP) execution, and mid-study amendments

Strong analytical mindset with sharp attention to detail

Trained in SAS, R, and/or Python

Data Programmer/Clinical Data programmer

t,Medidata Rave -EDC- Custom function Programming, GCP,UAT

custom function programming is mandatory

Good to have : SAS/R/Python