Senior Programmer Analyst

1 month ago

Bangalore, India Fortrea Full time

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.

Lead the development and implementation of Clinical solutions to global technical services issues and concerns regarding EDC tools or SAS programming.
♦ Lead the development of visual analytics dashboard using tools like Spotfire/Tableau.
♦ Complete assigned work utilizing Medidata Rave or Oracle InForm or other proprietary software according to Labcorp SOPs, Work Instructions, and project specific guidelines in accordance with Good Clinical Practices.
♦ Perform any post-production changes to the EDC database or enhancements to the SAS programs like SAS edit checks, listings, Protocol Deviations, etc.,
♦ With assistance, meet with Data Manager on assigned projects to discuss contractual obligations and timelines.
♦ Act as Subject Matter Expert (SME) and be point of contact for any technical services, issues related to EDC tools or SAS programming.
♦ Serve as Lead Statistical Programmer providing programming support for development and maintenance of SDTM/Client standards datasets.
♦ Develop/validate Custom/Complex SDTM domains and efficiently handle external data and data reconciliations.
♦ Develop and implement SDTM automation/standardization and best programming practices across projects to enhance quality and productivity.
♦ Plan, execute and oversee all programming activities on a study, including but not limited to, resource estimation, meeting timelines, maximizing quality, interaction with other departments and the client, etc.
♦ Exhibit good imparting, analytical skills along with testing, troubleshooting, error fixing, and documentation skills.
♦ Participate in the ongoing review of the processes used to ensure adaptation of best practices.
♦ Conduct Peer Review/Quality control of study design for assigned projects.
♦ Able to work independently and take initiative to accept new challenges in Clinical Programming Applications, also participate in the validation of new or updates to software.
♦ Maintain awareness of new developments in EDC products which may be applied to improve the efficient use of these systems.
♦ Resource forecasting and allocate activities to the team members on the project.
♦ Proactively identify trends, generate reports/metrics, or demonstrate programming process to sponsors/auditors (if required), assist with the design of ECRFs and other study documents.
♦ Perform other duties as assigned by Manager.

Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact.

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