Ankur Sharma
Associate Director, Statistical Programming & Technologies 1 at Bristol Myers Squibb
- Role
- Associate Director (Immunology, Cardiovascular, Fibrosis) at Bristol Myers Squibb
- Location
- Philadelphia, PA, US
- LinkedIn followers
- 500 followers
About Ankur Sharma
Accomplished Statistical Programming leader with a proven record of driving large scale, global regulatory submissions and advancing data driven decision making across multiple therapeutic areas. Demonstrates deep proficiency in SAS (SAS/GRAPH, SAS/STAT, SAS/SQL, SAS/BASE) and holds SAS® Base Programmer certification. Recognized expert in CDISC standards—SDTM, ADaM, CDASH—with extensive experience developing Define.xml and Define.pdf to support high quality, submission ready deliverables.Adept at leading and mentoring high performing programming teams across global locations, fostering a culture of collaboration, accountability, and technical excellence. Experienced in managing complex workloads, coordinating with cross functional stakeholders, and overseeing vendor/CRO partnerships to ensure timely, compliant, and high integrity outcomes. Skilled in setting strategic programming direction, optimizing workflows, and elevating organizational capabilities through structured training on CDISC methodologies.Brings deep expertise in Phase and post marketing clinical trials, PK/PD, NCA development, and the production of high quality TLGs. Known for strong leadership presence, operational rigor, and the ability to guide teams through fast paced, submission driven environments.
Experience
Associate Director (Immunology, Cardiovascular, Fibrosis)
Jul 2020 — Present · Princeton, NJ, US
Education
The University of Texas at Arlington
MS, Industrial Engineering, Statistics, Operations Research
2006 — 2008
Kurukshetra University
B.Tech, Instrumentation Engineering
2002 — 2006
Skills
- Clinical Data Management
- Oracle Clinical
- Biostatistics
- Data Management
- Validation
- Cdisc Standards
- Standard Operating Procedure (Sop)
- Pharmacovigilance
- Statistics
- Data Analysis
- Clinical Study Design
- Cdisc
- Clinical Trials
- Statistical Programming
- Pharmaceutical Industry
- Sop
- Fda
- Electronic Data Capture (Edc)
- Oncology
- 21 Cfr Part 11
- Gcp
- Clinical Development
- Data Validation
- Edc
- Therapeutic Areas
- Sas
- CRO Management
- Ctms
- Pharmaceuticals
- Sdtm
- Sas/Sql
- Ich-Gcp
- Clinical Research
- Sas Programming
- Crf Design
- CRO
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