Clinical (SAS) Programmer – Lead
J
JobgetherClinical research
Based in IndiaFull-TimeLead
Salary not disclosed
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Job Details
- Experience
- Extensive experience in clinical data programming
- Required Skills
- R
Requirements
- Bachelor's degree in Life Sciences, Computer Science, or a related discipline.
- Extensive experience in clinical data programming.
- Strong proficiency in SAS.
- Familiarity with R or other relevant programming languages.
- In-depth understanding of clinical trial data structures, clinical programming workflows, and statistical reporting requirements.
- Knowledge of CDISC standards, particularly SDTM and ADaM.
- Understanding of clinical research regulations and regulatory submission requirements.
- Experience developing and validating clinical datasets, tables, listings, and figures.
- Ability to provide technical guidance and mentor junior team members.
- Ability to manage multiple projects, competing deadlines, and changing priorities.
- Willingness to travel as required, approximately 10%.
Responsibilities
- Lead the design, development, and validation of clinical data programming solutions for clinical trials.
- Develop and validate clinical datasets, tables, listings, and figures (TLFs) according to study specifications and analysis requirements.
- Collaborate with biostatisticians, data managers, and clinical teams to define data specifications, programming requirements, and analysis plans.
- Apply quality control procedures and validation checks to ensure clinical data accuracy, consistency, completeness, and integrity.
- Apply clinical data standards and regulatory requirements throughout programming and validation activities.
- Manage day-to-day programming tasks, coordinate priorities, and deliver outputs on time.
- Provide technical leadership and mentorship to junior programmers.
- Resolve programming issues with cross-functional teams and improve workflows and delivery standards.
- Contribute to multiple clinical projects while managing competing priorities.
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