Clinical Database Programmer

Skill Set :Clinical Database Programmer Location : Pan India Experience :6-8 years Job Description We are seeking an experienced Clinical Database Programmer with expertise in Clinical Data Management (CDM) and Study Setup activities to support clinical trial database design, development, validation, and maintenance. The ideal candidate will have hands-on experience with EDC systems, study build activities, database programming, and clinical trial data management processes. Key Responsibilities Design, configure, and maintain clinical study databases in EDC systems. Perform study setup activities including eCRF design, edit checks, derivations, and database configuration. Develop and validate clinical databases according to protocol requirements and CDISC standards. Create and maintain study documentation, validation documents, and specifications. Perform User Acceptance Testing (UAT) and support database releases. Collaborate with Clinical Data Managers, Biostatisticians, Clinical Operations, and study teams. Ensure compliance with GCP, SOPs, and regulatory requirements. Support data cleaning, discrepancy management, and database lock activities. Troubleshoot database issues and implement corrective actions. Participate in study migration, amendments, and production deployments. Required Skills Strong experience in Clinical Data Management (CDM). Hands-on experience in Clinical Database Programming and Study Setup. Experience with EDC platforms such as: Medidata Rave Oracle Clinical Inform Veeva CDMS REDCap (preferred) Knowledge of eCRF design and Edit Check programming. Experience in UAT, validation, and database release processes. Understanding of Clinical Trial lifecycle and Data Management processes. Familiarity with CDISC standards (SDTM, CDASH). Strong analytical and problem-solving skills. Preferred Skills Experience in Life Sciences / Pharmaceutical / CRO environments. Knowledge of SAS, SQL, or reporting tools. Exposure to regulatory submissions and database lock activities. Good communication and stakeholder management skills. Skill Set :Clinical Database Programmer Location : Pan India Experience :6-8 years Job Description We are seeking an experienced Clinical Database Programmer with expertise in Clinical Data Management (CDM) and Study Setup activities to support clinical trial database design, development, validation, and maintenance. The ideal candidate will have hands-on experience with EDC systems, study build activities, database programming, and clinical trial data management processes. Key Responsibilities Design, configure, and maintain clinical study databases in EDC systems. Perform study setup activities including eCRF design, edit checks, derivations, and database configuration. Develop and validate clinical databases according to protocol requirements and CDISC standards. Create and maintain study documentation, validation documents, and specifications. Perform User Acceptance Testing (UAT) and support database releases. Collaborate with Clinical Data Managers, Biostatisticians, Clinical Operations, and study teams. Ensure compliance with GCP, SOPs, and regulatory requirements. Support data cleaning, discrepancy management, and database lock activities. Troubleshoot database issues and implement corrective actions. Participate in study migration, amendments, and production deployments. Required Skills Strong experience in Clinical Data Management (CDM). Hands-on experience in Clinical Database Programming and Study Setup. Experience with EDC platforms such as: Medidata Rave Oracle Clinical Inform Veeva CDMS REDCap (preferred) Knowledge of eCRF design and Edit Check programming. Experience in UAT, validation, and database release processes. Understanding of Clinical Trial lifecycle and Data Management processes. Familiarity with CDISC standards (SDTM, CDASH). Strong analytical and problem-solving skills. Preferred Skills Experience in Life Sciences / Pharmaceutical / CRO environments. Knowledge of SAS, SQL, or reporting tools. Exposure to regulatory submissions and database lock activities. Good communication and stakeholder management skills.