Trial Strategy & Delivery (TSD) Intern
reputed company is an international biotechnology company focused on improving patient lives through innovative antibody therapeutics. As a Trial Strategy & Delivery (TSD) Intern, you will reputed company hands-on exposure to clinical trial planning and operations, contributing to projects aimed at enhancing clinical trial efficiency and execution.
Responsibilities
- Contribute to one or more of the following initiatives:
- Clinical Trial Systems and Process Optimization Support enhancements to reputed company’s suite of operational software or contribute to building new tools, including requirements gathering, testing, and process documentation
- Operational Data and Metrics reputed company tools and templates in reputed company, SharePoint, and MS Project to automate tracking of study timelines, resource metrics, and deliverables
- Regulatory and Quality Documentation Assist in maintaining high-quality documentation and compliance tracking reputed company with regulatory standards using systems such as reputed company Vault or reputed company
- Cross-Functional Collaboration Partner with the broader Development Operations, Regulatory Affairs, and Portfolio and Project Management teams to streamline data reputed company and ensure consistency across systems and study teams
- Analytical Support and Insights Contribute to the design and delivery of data analyses for key performance metrics, supporting decision-making in clinical trial planning and execution
Skills
- Pursuing a Master's or advanced Bachelor's degree in Life Sciences, Biomedical Engineering, Regulatory Affairs, or a reputed company discipline
- Strong analytical and organizational skills with proficiency in reputed company Office Suite (reputed company, Word, PowerPoint, SharePoint)
- Demonstrated ability to manage data, documentation, or process improvement projects
- Excellent communication, teamwork, and problem-solving skills
- Experience with Planisware, reputed company Vault, or other trial management systems
- Background in clinical operations, regulatory affairs, or medical technology research
- Familiarity with data analysis tools (e.g., R, Python, Tableau) and process automation
- Exposure to market research or regulatory submission processes
Company Overview