This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Sr. Stat Programmer Clin Pharm based in India.
This role offers the opportunity to contribute to global clinical research by transforming complex clinical trial data into meaningful statistical outputs.
The professional will support pharmaceutical development programs through advanced SAS programming, data analysis, and quality-focused deliverables.
You will collaborate with statisticians, programmers, and clinical project teams to ensure accurate and compliant reporting.
The position combines technical expertise, scientific understanding, and leadership within a fast-paced life sciences environment.
The ideal candidate will bring strong clinical programming experience, attention to detail, and the ability to manage multiple priorities.
This is an opportunity to help accelerate healthcare innovation while supporting the development of therapies that improve patient outcomes worldwide.
This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Sr. Stat Programmer Clin Pharm based in India.
This role offers the opportunity to contribute to global clinical research by transforming complex clinical trial data into meaningful statistical outputs.
The professional will support pharmaceutical development programs through advanced SAS programming, data analysis, and quality-focused deliverables.
You will collaborate with statisticians, programmers, and clinical project teams to ensure accurate and compliant reporting.
The position combines technical expertise, scientific understanding, and leadership within a fast-paced life sciences environment.
The ideal candidate will bring strong clinical programming experience, attention to detail, and the ability to manage multiple priorities.
This is an opportunity to help accelerate healthcare innovation while supporting the development of therapies that improve patient outcomes worldwide.
Accountabilities:
- Develop custom programming solutions using SAS or other statistical programming tools to generate tables, listings, graphs, and derived datasets according to statistical analysis plans and programming specifications.
- Perform validation programming, quality checks, and issue resolution in collaboration with programmers, biostatisticians, and clinical project teams.
- Ensure programming outputs meet quality standards, project requirements, and applicable regulatory guidelines, including ICH standards and internal procedures.
- Maintain complete and accurate project documentation, testing records, verification materials, and programming documentation to ensure inspection readiness.
- Manage programming activities across multiple projects, balancing timelines, priorities, and changing business requirements.
- Create specifications for datasets and outputs of varying complexity while anticipating potential programming challenges and reducing rework.
- Act as a lead statistical programmer by coordinating programming activities, reviewing deliverables, and supporting project execution.
- Review key project documents such as Statistical Analysis Plans, mock shells, programming specifications, annotated CRFs, and database designs.
- Participate in sponsor meetings, project kickoffs, and bid defense meetings as a statistical programming representative when required.
- Mentor and support other programming professionals through training, feedback, knowledge sharing, and technical guidance.
- Collaborate effectively with internal teams by organizing meetings, tracking action items, and supporting shared project objectives.
- Bachelor’s degree, preferably in a scientific, statistical, or related discipline; equivalent education and demonstrated programming experience may also be considered.
- Extensive experience with SAS programming or other statistical programming tools, preferably within a clinical trial environment.
- Strong understanding of clinical research processes, statistical programming workflows, and regulatory expectations.
- Ability to create and validate clinical trial datasets, reports, and statistical outputs with a high level of accuracy.
- Excellent written and verbal communication skills.
- Strong organizational skills with the ability to manage multiple projects, deadlines, and priorities effectively.
- Ability to work collaboratively with cross-functional teams, including statisticians, programmers, and clinical stakeholders.
- Ability to read, write, speak, and understand English fluently.
- Experience leading programming activities or mentoring other team members is preferred.
- Fully remote work opportunity based in India.
- Opportunity to contribute to global clinical research and healthcare innovation.
- Professional development opportunities through training, mentoring, and technical growth initiatives.
- Exposure to complex clinical trial programs and collaboration with international teams.
- Supportive environment focused on knowledge sharing, innovation, and career progression.
- Opportunity to work with experienced professionals across life sciences and healthcare domains.
- Comprehensive rewards and recognition programs.