Are you looking to join a company where your contributions truly matter and where you ll be part of a supportive innovative team MMS is a award-winning data-focused clinical research organization CRO We pride ourselves on being a Outstanding Place to Work certified organization recognized for our exceptional culture and industry best employee retention rate We support the pharmaceutical biotech and medical device industries with our proven scientific approach to complex trial data and regulatory submission challenges With a global footprint across four continents MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive Join us at MMS and be part of a team that is shaping the future of clinical research Discover more about our exciting opportunities and why MMS is a great place to advance your career Visit or follow MMS on Participates in protocol review with clients provides suggestions regarding ability to capture protocol information in database successfully Contribute to study tracking and metric reports for use by the study team Contribute to CRF tracking and data entry integration of external electronic data data validation and review query processing and resolution adverse event and medication coding SAE reconciliation database lock and database QC audits Contribute to user acceptance testing UAT of EDC and integrated systems including executing of test plan and scripts Assist with preparation for training sites users training on EDC applications and UAT End user knowledge for study conduct activities including queries management standard reporting and extracting data in multiple EDC systems Independently develops data entry screens dynamics edit checks and other EDC components in multiple EDC systems Ability to program using SQL SAS or another programming language Provides input to resolve issues in data management study processing activities Develops appropria