Are you seeking a purposeful and rewarding SAS programming career opportunity?
Our eCOA team is growing in India, and with big ambitions and a clear vision for the future, now is the time to join Clario as a Systems Analyst II.
What we offer
- Competitive compensation + shift allowances
- Attractive benefits (security, flexibility, support and well-being)
- Engaging employee programs
- Technology for hybrid working and great onsite facilities
What you'll be doing
Create, maintain and test code used for non-standard data file creation as well as for CDISC SDTM datasets; mentor System Analyst I staff; programming resource for Clinical Data Operations staff and other departments as needed including creation of statistical and submission-ready datasets.
- Attend client meetings as appropriate to understand data collection requirements for the protocol.
- Receive and review standard Clario/non-Clario standard client file specifications from Data Manager/Project Manager or client and interact with the client to finalize transfer specifications.
- Develop and validate programs to create non-standard data files as well as CDISC SDTM compliant datasets.
- Create submission-ready datasets for eCOA trials (SDTM QS)
- As part of the Software Development Life Cycle, develop and unit test code, create and execute test scripts and perform peer review.
- Process data extracts, review encoding requests daily to run encoding programs and archive studies.
- Performing ad-hoc programming activities utilizing raw data based on internal and external requests for:
- Esoteric quality control checks.
- Data resolution/mining.
- Treatment emergent flags and other specifications per Statistical Analysis Plan.
- Other client requirements.
- Work with data management in providing programming support for DM activities including data review.
- Prepare and participate in internal and external audits.
- Work across multiple service lines and modalities.
- Work hand in hand with a cross functional teams (Data Managers, Project Managers and other industry experts) for project delivery - for example to support New Product Initiatives and Minimum Viable Product solutions.
- Identify opportunities to improve the methodology and provide practical solutions for problems.
- Contribute to the development of best practice to improve quality, efficiency and effectiveness.
- Assist with orientation and training of CDP and Data Management / Project Management personnel as determined by management.
- Mentoring System Analyst I and other CDP resource.
- Contribute to process development.
- Review and development of SOPs and associated documents related to CDP activities. Maintain working knowledge of CDISC SDTM standards and recommend changes to processes and standard specifications as needed.
- Complete administration tasks as needed within CDP.
What we look for
- SAS Certified Specialist: Base Programming.
- SAS Certified Professional: Advanced Programming is a plus.
- Bachelorโs or Masterโs degree in Informatics, Mathematics, Computer Science or other relevant qualification.
- Ideally three or more years of experience in a Pharmaceutical company or a CRO as a SAS Programmer - experience in SAS/BASE, SAS Macros and SAS SQL procedures and one or more years experience in database design and data structures.
- Understanding of the pharmaceutical drug development process, as gained through a minimum of two years experience in the pharmaceutical or healthcare industry.
- Proven experience working with large, complex, real-world data sets (more specifically patient data).
- Extensive experience in implementing CDISC SDTM and Define standards. Working knowledge of CM, EX, FA, QS CDISC domains would be valuable.
- Knowledge of technical and regulatory requirements related to the role.
- Excellent time management skills, contributing to multiple projects with competing timelines.
- Assist in developing and delivering training.
- Experience with Windows and Microsoft Office products.
- Experience with DB programming is a plus.
These positions are subject to European and US working hour shift patterns, and are considered hybrid remote working roles from our offices in VG Heritage, 18/2, 18/3, Vani Vilas Road, Basavanagudi, Bangalore 560004.