Clinical Trial System Professional

As a Clinical Data Standards/Clinical Programmer at our company, you will play a crucial role in ensuring the adherence to CDISC standards (CDASH, SDTM, ADaM, ARDS) and maintaining a valuable understanding of the clinical trial lifecycle. Your responsibilities will include clinical data programming, standards implementation, dataset validation, metadata management, and supporting regulatory submissions. It is essential for you to have experience collaborating with cross-functional teams and be comfortable working in customer-facing environments within pharma, biotech, or CRO industries. Your robust analytical, communication, and problem-solving skills will be put to good use in this role. Key Responsibilities: - Implement CDISC standards such as CDASH, SDTM, ADaM, ARDS - Perform clinical data programming tasks - Validate datasets and ensure accuracy - Manage metadata effectively - Support regulatory submissions Qualifications Required: - Minimum of 4 years of experience in a similar role - Solid knowledge of CDISC standards - Intermediate SQL skills - Experience working in pharma, biotech, or CRO industries - Strong analytical, communication, and problem-solving skills Please note that the job posting has been aggregated from an external source, and role details, content, and availability are subject to change. We recommend verifying the latest information directly on the company website before applying. As a Clinical Data Standards/Clinical Programmer at our company, you will play a crucial role in ensuring the adherence to CDISC standards (CDASH, SDTM, ADaM, ARDS) and maintaining a valuable understanding of the clinical trial lifecycle. Your responsibilities will include clinical data programming, standards implementation, dataset validation, metadata management, and supporting regulatory submissions. It is essential for you to have experience collaborating with cross-functional teams and be comfortable working in customer-facing environments within pharma, biotech, or CRO industries. Your robust analytical, communication, and problem-solving skills will be put to good use in this role. Key Responsibilities: - Implement CDISC standards such as CDASH, SDTM, ADaM, ARDS - Perform clinical data programming tasks - Validate datasets and ensure accuracy - Manage metadata effectively - Support regulatory submissions Qualifications Required: - Minimum of 4 years of experience in a similar role - Solid knowledge of CDISC standards - Intermediate SQL skills - Experience working in pharma, biotech, or CRO industries - Strong analytical, communication, and problem-solving skills Please note that the job posting has been aggregated from an external source, and role details, content, and availability are subject to change. We recommend verifying the latest information directly on the company website before applying.