C&SP Intern

Overview

Support data analyses and reporting activities within clinical trials as an individual contributor on the programming team, supporting programming activities of low to medium complexity trials.

What you'll do

• Complete and, where needed, lead programming trial activities of low to medium complexity and/or criticality, with high quality and timeliness of deliverables.
• Be accountable for the design and development of programs in support of clinical research analysis and reporting.
• Perform an appropriate level of verification of programming and reporting activities; review and provide input on project requirements and documentation.
• Support submission activities, including creation, verification and delivery of CDISC compliant and/or non-standard data packages and reviewer's guides.
• Follow departmental processes and procedures, ensure use of the latest standards and deploy current technologies.
• Contribute to departmental innovation and process improvement projects.
• Collaborate effectively with team and cross-functional members.
• Ensure continued compliance with required company and departmental training, time reporting and other business/operational processes.

What you'll need

• Bachelor's degree or higher and/or equivalent in computer science, data science/data engineering, mathematics, public health, or another relevant scientific field (or equivalent theoretical/technical depth).
• Approx. 2+ years of relevant programming experience.
• Basic knowledge of regulatory guidelines (e.g. ICH-GCP) and relevant clinical R&D concepts.
• Excellent written and verbal communication skills.
• Knowledge of data structures and relevant programming languages for data manipulation, statistical analysis and reporting, which may include SAS, R, Python, etc.
• Basic knowledge of processes, methods, and concepts relevant to programming.

Nice to have

• Experience in the Pharmaceutical, CRO or Biotech industry or a related field or industry.
• Experience working in a team environment.
• SAS knowledge for the Clinical Programming role.

Details

• Location: Hyderabad, Andhra Pradesh, India.
• Reports into a people manager position within the Delivery Unit and is accountable to the Portfolio and Study Leads for assigned activities.