Manager, Clinical Data Reporting

About Bristol Myers Squibb We are a global biopharmaceutical company whose mission is to discover develop and deliver innovative medicines that help patients prevail over serious diseases Headquartered in New York City we are one of the world s largest pharmaceutical companies who have been fortunate to consistently rank on the Fortune 500 list of companies in the US About Bristol Myers Squibb Hyderabad BMS Hyderabad is an integrated global hub where our work is focused on helping patients prevail over serious diseases by building sustainable and innovative solutions With our commitment to invest 100 million in Hyderabad over the next 3 years this important science technology and innovation centre will support a range of technology and global drug development activities that will help us usher in the next wave of innovation Test developed reports document results and provide peer review support as needed Adhere to documentation and process compliance notifying management of any noncompliance Analyse clinical trial needs holistically to determine effective monitoring approaches and ensure patient safety Negotiate with stakeholders and foster collaboration for efficient report delivery Prioritize deliverables based on business criticality and seek assistance when needed Demonstrate technical expertise to develop solutions for complex reporting needs Work cohesively with team members embracing feedback and suggestions Keeping up to date with new reporting tools techniques and industry trends to enhance skills and knowledge Ensure compliance with procedures trainings and policies defined by the organization Contribute to other sub-functions of CDR A as needed to support business priorities Flexible to work with global stakeholders across different time zones while ensuring business continuity Degree Requirements BS computer science Maths Stats Life Sciences programming data management scientific or analytic discipline Experience Requirements 5 years experience in the development of reporting and analytics in the Pharmaceutical Industry with a focus on clinical trials Key Competency Requirements Primary technical Skills Experience with various reporting and analytic tools like SAS Qlik SQL PLSQL and added advantage if experienced in eClinical tool elluminate Mapper Hands on experience in SDLC Software Development Life Cycle process Strong understanding of relational databases and ETL concepts Secondary Technical skills Good to have hands on Knowledge of JReview Spotfire Tableau Power BI Micro Strategy Yellowfin or any visualization development tool and or programming languages such as Python NumPy and Pandas R and R Shiny Domain skills Good understanding the various clinical data sources such as EDC Central lab Local Lab Medical Imaging IVRS IRT ECG CTMS and so on Knowledge of CDISC standards SDTM domains with additional advantage if worked on SDTM transformations Therapeutic Area knowledge in the clinical domain Must be capable of reading and understanding a clinical trial protocol and collaborating with the clinical trial team in understanding the reporting needs Good understanding of the clinical study database design in RAVE Veeva Oracle Clinical and or any other study design EDC system Thorough understanding of Drug Discovery process and regulatory requirements ICH FDA Soft Skills Analytical thinking The ability to think critically and analyze complex data sets identifying patterns trends and insights to solve problems and make data-driven decisions with some guidance from seniors Attention to detail Must be attentive to the details during the requirements gatherings and effective communication of the actions and effective follow up thus ensuring accuracy and precision in data interpretation and reporting Communication skills Effectively conveying complex technical concepts and findings to both technical and non-technical stakeholders including presenting data visually and using storytelling techniques to make data more accessible and understandable