Senior Clinical SAS Programmer | SDTM, ADaM & TLFs | 14+ Years Experience

I am a Senior Clinical SAS / Statistical Programmer with over 14 years of experience
supporting global pharmaceutical companies and CROs across the clinical trial lifecycle.

My core expertise includes SDTM and ADaM dataset development, TLF programming
(Tables, Listings, and Figures), QC and validation, and regulatory submission
support in compliance with CDISC standards (SDTM, ADaM, and Define.xml).

I have worked on multiple therapeutic areas and am comfortable collaborating
with cross-functional teams, sponsors, and CRO partners. I can support both
project-based work and long-term contract engagements as a dedicated resource.

I am based in India and available for remote work with global teams, ensuring
high-quality, timely, and regulatory-compliant deliverables.

Clinical SAS • Statistical Programming • SDTM • ADaM • TLFs • CDISC • Pharma • CRO • Contract • Dedicated Resource

Work Terms

Hours of Operation:
I am available Monday to Friday, with flexibility to overlap with US and Europe time zones as required.

Availability:
20–40 hours per week for contract or dedicated resource engagements.
Project-based support is also available.

Payment Terms:
Hourly or fixed-price engagements. Payments to be made via Guru SafePay.
Rates are negotiable for long-term contracts.

Communication:
Preferred communication via email, Guru messaging, or video calls (Zoom / Microsoft Teams).
Regular status updates and timely responses are ensured.

Work Style:
I work independently with minimal supervision, follow SOPs and timelines,
and ensure high-quality, regulatory-compliant deliverables.