Location: Bangalore/ Mumbai /Hybrid/WFHExperience: 3 to 6 yearsJob Responsibilities: Strong oral and written communication skills Study Lead Experience and exposure on efficacy domains and TFLs is a plus Participates in the creation or validation of Case Report Forms (CRFs), CRF annotations, SDTM/ADAM specifications, datasets, Define, and TLFs. Proficiency in SAS and CDISC for programming. Ensure all statistical activities are in accordance with internal and external quality standards, SOPs/WPDs, ICH-GCP, and/or other international/local regulatory requirements. Experience in specialized therapeutic areas (TAs) such as oncology, immunology, and neurology would be a plus.Core Strength: The candidate should be technically sound and have hands-on experience in Statistical Programming. Ensures excellence and high quality in work. Problem-solving approach. Act as a good team player and quick learner.
Job Title
Clinical SAS Programmer