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Programmer (SAS - Clinical Trials) in Bengaluru, India - Jobeax

Programmer (SAS - Clinical Trials) in Bengaluru, India is listed on Jobeax. Browse 30,000+ vacancies available.

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Join Us as a CDM Programmer II - Make an Impact at the Forefront of Innovation
We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.
As part of our expert team, you'll have the opportunity to ensure operational excellence that makes a real difference in clinical trials. As a CDM Programmer II, you will work with clinical data management systems and programming tools to provide advanced programming support in data management activities and deliverables. This includes, but is not limited to, database development, data validations, and assisting with defining tools and techniques for improving process efficiencies. You will work within a multi-disciplinary project team to complete assigned tasks on time and within budget.
Performs tasks following within the timelines established by the team, in accordance with the process outlined in the departmental procedures and indicated by the project contract.

Designs, builds and tests project databases & edit checks.
Defines and imports data into the system.
Defines, creates and tests listings for data review and performs programming activities in line with project requirements.
Acts as the lead on studies of simple to moderity complexity with close supervision. Researches and leverages resources to resolve issues and manage moderately complex tasks through the development and application of new knowledge and/or professional skills in areas including programming and technology.
Increases knowledge and skills to gain good understanding of the lead programmer roles and overall department processes.
Ensures adherence to departmental working practice documents and SOPs, and contributes to the development informal training materials.

Education and Experience Requirements:
Bachelor's degree or equivalent and relevant formal academic / vocational qualification
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years').
Experience in Medidata Rave with custom Functions development or Veeva with CDB expertise.
Clinical Data Management domain experience
Database build and study configuration experience

In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Solid written, verbal and computer skills

Basic experience in one or more programming languages or relational database systems (RDBMS) and structure
Working knowledge of programming tools SAS, SQL, Crystal Reports, and JReview
Demonstrated leadership ability and ability to work on a multi-disciplinary project team
Excellent project management skills, such as project budget creation, including modifying for project updates, and managing project budgets and risks
Capable of interpreting and contributing to company policies
Delivery and quality driven

Work is performed in an office environment with exposure to electrical office equipment.
. Occasional drives to site locations with occasional travel both domestic and international.

When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You'll work in an environment where collaboration and development are part of the everyday experience-and where your contributions truly make a difference.
Apply today to help us deliver tomorrow's breakthroughs.

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