Taniya Muliyil
Hillsborough,NJ
Summary
Statistical Programming leader with experience in building winning teams and developing individuals into leadership positions. Experience working on various therapeutic areas including oncology, immunology, cardiovascular along with helping strategize formation of new neuroscience TA at BMS. Business process owner for SDLC process. Led various process improvements like Development and Verification of statistical programming deliverables, data masking process at BMS, risk -based verification process. Lead teams to successful submissions. Standards representative involved in developing standards and interactive visualization tools that can reduce costs and bring in efficiency.
Overview
16
16
years of professional experience
Work History
Associate Director, Statistical Programming
Bristol Meyers Squibb
08.2018 - Current
- Manage/Retain/Hire and develop programmers in CV/NS Therapeutic Area (Managing 6 direct reports) Managing teams across different time zones Lead standards and automation for CV/NS TA along with building robust processes Providing input on CRF library creations for Neuroscience
- Played a key role in building end to end standards from CRF/digitalization of protocol to submission readiness
- Strategize development of new Neuroscience TA within BMS Collaborate with other programming leaders to develop best practices across the organization and lead global initiatives
- Involved in global initiatives to enhance data visualization /automation /streamlining process
- Led teams to successful NDA submissions in immunology ensuring quality of esub deliverables
- Business Process Owner for SDLC process responsible for development/verification of statistical programming deliverables
- Played key role in vendor management and oversight of vendor deliverables.
Manager, Statistical Programming
Covance Inc
08.2017 - 08.2018
- Led and supervised statistical programming activities for oncology studies
- Responsible for managing programming resources, budgeting, and timelines for studies across therapeutic areas
- Interact with cross functional team and functional heads from Global Project Teams, Project Management, Medical Affairs, Regulatory Affairs and Quality Assurance Represent the department and the company in client meetings/presentations and maintain a positive working relationship with sponsors, collaborating associates, and vendor personnel
- Conduct annual review and performance evaluations for direct reports
- Identify project priorities and project timeline goals and communicate priority related issues and timelines to programming teams
- Ensure the efficiency, quality, and integrity of data reporting, and project activities executed.
Principal Programmer
Novartis Pharmaceuticals
10.2012 - 08.2017
- Manage and mentor contractors and FSP staff globally
- Point of contact for resolving technical issues and providing necessary advice
- Standardize timelines for short duration PK/ PD studies following CDISC standards
- In conjunction with the Biometrician/ Statistical Scientist, developing study-level programming standards and ensuring compliance with project-level/company standards
- Played a key role in data transfer process for GSK trials during merger of Novartis with GSK oncology
- Supported different submissions to FDA and PMDA
- Led many quality initiatives for programmers across multiple sites.
Senior Statistical Programmer
PPD Inc
05.2011 - 10.2012
- Developed standard macros to ensure automation of outputs thereby increasing efficiency
- Worked on number of submission projects and health authority requests
- Worked on generating complex pooled data set for ISS/ISE analysis
- Interacted with clients, participated in meetings with project statisticians, clinicians, and programmers.
Contractor
Bristol Meyers Squibb
08.2008 - 05.2011
- Worked in proximity with biostatisticians to review Protocol, SAP and CRF Reviewed submission package and provided input to the team
- Acted as SME for CDISC related issues
- Worked in proximity with biostatisticians to review Protocol, SAP and CRF
- Worked on generating pooled analysis datasets for complex ISS/ISE analysis.
Contractor
Kendle International
02.2008 - 08.2008
- Worked on generating submission package (define.xml, SDTM, ADAM, SDRG, ADRG) Responsible for creating programming specifications and pooled datasets for complex ISE and ISS analysis Converting legacy studies to CDISC standards
- Responsible for Ad-hoc report generation to address health authority questions.
Education
M.S. in Applied Statistics -
Penn State University
M.S. in Biology -
The University of Texas at Arlington
M.S. in Biotechnology -
Madras University, Chennai, India
Skills
- Project Management
- Budget Management
- Strategic leadership
- Resources Allocation
- Process Improvement
- Analytical Thinking
- Critical Thinking
- Team Collaboration and Leadership
- Decision-Making
- Budget Development
- Hiring and Training
Publications
- Jorge Ernesto Quezada-Díaz, Taniya Muliyil, Javier Río, and Esther Betrán. Drcd-1 related: a positively selected spermatogenesis retrogene in Drosophila. Genetica. 2010 Oct; 138(9-10): 925–937.
- Pharma SUG 2020-Oncology Graphs-Creation (Using SAS and R), Interpretation and QA
Timeline
Associate Director, Statistical Programming
Bristol Meyers Squibb
08.2018 - Current
Manager, Statistical Programming
Covance Inc
08.2017 - 08.2018
Principal Programmer
Novartis Pharmaceuticals
10.2012 - 08.2017
Senior Statistical Programmer
PPD Inc
05.2011 - 10.2012
Contractor
Bristol Meyers Squibb
08.2008 - 05.2011
Contractor
Kendle International
02.2008 - 08.2008
M.S. in Applied Statistics -
Penn State University
M.S. in Biology -
The University of Texas at Arlington
M.S. in Biotechnology -
Madras University, Chennai, India
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