Merck Group is Hiring Specialist, Program and Application Development

Responsibilities :

1.     Develop, validate, document, and maintain program(s) and applications required to conduct or support clinical data quality checking and surveillance for clinical trials and/or programs, (e.g DQSP, CQR, coding checks, SQSP, SDTM checker, SAE/external data reconciliation, required reports, listings or figures with SAS, R or other programming languages)
2.     Create, validate, document, and maintain data conversion programs, follow company level standard.
3.     Run (the developed) tools, programs and macros according to timelines communicated by the ordering client/role
4.     Ad hoc programming requests (e.g data format transfer and data pooling per request)
5.     Contribute to the continuous improvement, re-engineering and implementation of processes, tools, technologies, conventions, standards, policies, Standard Operating Procedures (SOPs), and Working Instructions (WIs) as needed
6.     Works effectively in a mixed environment and uses best practices and knowledge to improve products or services and to define processes and standards.
7.     Solves moderate complexity problems based on advanced to sophisticated analytical skills and complex judgement.
8.     Accountable for the quality of on-going activities/processes. Receives minimal guidance or works independently.
9.     Contribute as team member to DMMI initiatives
10.     Develop experience and skills in new systems when necessary
11.     Keep up to date with job related topics, in particular with regard to SAS, R and Spotfire and other potential language and applications
12. Develop and maintain standard libraries including e-CRFs, edit checks and programs within EDC and other relevant DMMI systems.
13. Deliver high quality and timely database design deliverables and ensure the database readiness
14. Conduct system validation as needed
15. Mentor other DBDs in all aspects of DMMI process, as needed
16. Assume the role of EDC Specialist/EDC Lead User if required

Requirements :

1. Comprehensive knowledge of SAS/BASE, SAS/Macro and R. knowledge of SQL, Python or other programming languages is a plus
2.     Good Knowledge of EDC (e.g Inform, Medidate Rave, Oracle RDC)
3.     Comprehensive Knowledge of CDISC in general and comprehension of SDTM and define.xml
4.     Good Knowledge of regulations and guidance regarding clinical development, the systems used in this context and data management related aspects of e-submissions
5.     Good team player works effectively in international teams, and multi-disciplinary groups.
6.     Excellent accuracy and attention to detail
7.     Experience in leading low to moderate complexity projects with limited support from the supervisor
8. Database Developer:
9.     Comprehensive experience on database development (e.g Medrio, Inform, Medidata Rave, Oracle RDC)
10.     Comprehensive Knowledge of CDISC in general and comprehension of CDASH

Please share me your profile to  Yamini.Suvarchala@external.merckgroup.com

or

Apply through this link : click here..