SIRO Clinpharm - JReview Programmer - Clinical Data Management

Job Description : We are seeking a skilled and detail-oriented JReview Programmer with expertise in SAS/SQL to join our team. This role involves managing data extraction, transformation, and visualization activities while ensuring the accuracy and quality of deliverables. The ideal candidate will be proficient in working independently and collaboratively with cross-functional teams, particularly in clinical data management. Key Responsibilities : - Program Listings and Mappings : Develop and maintain program listings and mappings that meet study specific requirements. - Create Visualizations : Design and implement visualizations to aid in the interpretation of clinical data. - Clinical Data Review in JReview : Utilize JReview for hands-on clinical data review, ensuring data accuracy and compliance with project specifications. - Automation of Tasks : Implement automation techniques to streamline data handling processes and enhance efficiency. - Data Extraction and Transformation : Configure data extraction and transformations across multiple data sources at the study level as defined by the Data Transfer Agreement (DTA) and specifications provided by Data Engineers. - Stakeholder Collaboration : Partner closely with internal and external stakeholders, including Data Engineers, to ensure data integrity and accuracy. - Quality Deliverables : Ensure accurate delivery of data formats and data frequency with high-quality outputs per specifications. - Standards Development and Training : Participate in the development, maintenance, and training activities related to transfer specifications, best practices, and standards utilized by the business. Additional Activities : - Quality Review Assistance : Assist in quality review activities performed by vendors, ensuring adherence to specifications and standards as required. - Regulatory Compliance : Adhere to Standard Operating Procedures (SOPs) for computer system validation and comply with all Good Clinical Practice (GCP) regulations. - Training and Learning Compliance : Ensure compliance with personal Learning Curricula, corporate policies, and applicable GxP requirements. - Additional Duties : Perform other assigned duties within defined timelines to support project goals. Qualifications : - Bachelor's degree in Computer Science, Data Science, Life Sciences, or a related field. - Proven experience as a JReview Programmer with strong SAS and SQL skills. - Hands-on experience with clinical data review and visualization tools. - Familiarity with data extraction, transformation, and loading (ETL) processes. - Strong knowledge of GCP and computer system validation processes. - Excellent analytical and problem-solving skills. - Ability to work independently as well as collaboratively in a team environment. - Strong communication skills and the ability to interact with stakeholders at all levels. Preferred Skills : - Experience working in a clinical or pharmaceutical environment. - Knowledge of data standards and transfer specifications commonly used in clinical trials. - Familiarity with automation tools and techniques relevant to data processing. Why Join Us? - Opportunity to work with cutting-edge technologies and contribute to impactful clinical research. - Collaborative work environment with a focus on innovation and continuous learning. - Competitive salary and benefits package (ref:hirist.tech)

Location: arunachal-pradesh, IN

Posted Date: 11/22/2024