Overview
On Site
Full Time
Skills
Regulatory Affairs
Quality Assurance
Regulatory Compliance
Quality Control
Documentation
Leadership
Computer Science
Biostatistics
Life Sciences
FOCUS
Pharmaceutics
Biotechnology
Programming Languages
R
Microsoft Windows
Unix
SAS/BASE
SAS/MACROS
SAS/GRAPH
SAS/SQL
SAS
GRID
SAS Enterprise Guide
MedDRA
CDISC
SDTM
NDA
Communication
Collaboration
Attention To Detail
EDC
Oracle Clinical
TIBCO Spotfire
Tableau
Neuroscience
Job Details
Responsibilities:
- Lead the development and implementation of submission-ready SDTM datasets in accordance with regulatory requirements (e.g., FDA, EMA, PMDA).
- Collaborate with regulatory affairs and quality assurance teams to ensure compliance with submission guidelines and standards.
- Perform thorough quality control checks to validate the accuracy and completeness of submission datasets.
- Coordinate the preparation and documentation of submission packages, including data specifications and validation documentation.
- Serve as a subject matter expert on submission-related matters, providing guidance and support to cross-functional teams.
- Stay abreast of evolving regulatory requirements and industry best practices realeted.
to SDTM and submission standards.
- Bachelor's or master's degree in a relevant field (e.g., Computer Science, Biostatistics, Life Sciences).
- Minimum of 8 years of experience in Statistical & Clinical programming, with a focus on submission expertise, within the pharmaceutical or biotechnology industry.
- Proficiency in programming languages such as SAS and R.
- Strong knowledge in Windows and UNIX environment, with proficiency in SAS/Base, SAS Macros, SAS/Graph, SAS/SQL, SAS Grid, SAS Enterprise Guide, CDISC, SDTM, MedDRA, WHO DRUG;
- Deep understanding of CDISC standards and regulatory submission requirements.
- Proven experience in preparing and submitting SDTM datasets for regulatory filings (e.g., IND, NDA, BLA).
- Excellent communication and collaboration skills, with the ability to work effectively in a cross-functional environment.
- Strong attention to detail and a commitment to ensuring the quality and integrity of submission datasets.
- Experience with EDC systems (e.g., Medidata Rave, Oracle Clinical) and other tools (Jreview, Spotfire, Tableau) is a plus.
- Experience with Oncology and Neuroscience Therapeutic areas is plus
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