JD:
Required Skills
Strong programming expertise in R Programming with the ability to upskill to a proficient level quickly.
Hands-on experience in ADa M dataset creation and TLF (Tables, Listings & Figures) programming.
Good understanding of clinical trial data standards and regulatory requirements.
Ability to perform data validation, quality checks, and support statistical analysis activities.
Experience working with clinical study teams, biostatisticians, and data management teams.
Strong analytical, problem-solving, and communication skills.
Preferred Skills
Advanced to expert-level knowledge in R Programming.
Experience in:
ISS/ISE (Integrated Summary of Safety / Integrated Summary of Efficacy)
Regulatory Submissions
RTQs (Regulatory/Reviewer Query support)
Familiarity with Agile ways of working , including sprint planning, backlog management, and collaborative delivery models.
Prior experience working with GSK tools, standards, and pro...