Clinical Programmer - India

Worldwide Clinical Trials2 LocationsonsiteSalary not postedView the original posting at Worldwide Clinical Trials ↗

Who we are We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence. We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way. Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit. Why Worldwide We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us! *SUMMARY: To co-ordinate and perform processes associated with the configuration, maintenance and validation of databases and database systems and associated applications. * *RESPONSIBILITIES:* _Tasks may include but are not limited to:_ To liaise with relevant staff to determine the allocation of tasks, to establish timelines, to report progress and any issues outstanding. To review specifications for the set-up and modification of project specific data entry software (including edit check specifications). Review validation plan for edit check and reconciliation check specifications. Develop, test and run SAS programs for clinical data management. This includes programs for data validation and reconciliation checks, data listings and data transfers. To configure database/eDC software (both internal and 3rd party) for the use of DM, sponsor and sites To perform testing of databases and related applications according to IT and Data Management departmental SOPs, both for initial set-up and maintenance. To run database upload programs and to process any error reports. To liaise with 3rd party vendors to resolve issues, implement changes to software To liaise with Sponsors or their designates on matters associated with the transfer of electronic data to or from the company, as defined by the Director, Data Management. To support DM in the production and maintenance of system procedures and documentation Assist with Quality Assurance and Audit requirements Perform other duties as assigned. The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive. *OTHER SKILLS AND ABILITIES: * Be able to demonstrate good written and verbal communication skills. Be able to demonstrate a methodical and logical approach to problem solving and the ability to learn new tasks quickly. Be able to work with close attention to detail Be questioning about the validity of data being entered/extracted. Be hardworking and efficient. Possess good team working skills. Key competencies in customer focus, delivering on commitments, building strong relationships, communicating and influencing, and embracing innovation and change. The job holder must be computer literate and numerate with a willingness to adapt to various computer systems *REQUIREMENTS:* Be educated to degree level Have a experience of Data Management Systems and Software An understanding of CDISC SDTM standards Experience of SAS programming language Promotion to the next level is not automatic based on years of experience. Personnel are evaluated on proven competency, level of responsibility to work independently. We love knowing that someone is going to have a better life because of the work we do. To view our other roles, check out our careers

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