
Senior Data Analyst
6 days ago
Role Overview:
We are seeking a seasoned statistical programmer to lead the development of clinical trials in a fast-paced pharmaceutical environment.
This role is ideal for an experienced professional with advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM).
The successful candidate will leverage their expertise to support or lead one or more Phase I-IV clinical trials, utilizing data manipulation, analysis and reporting to drive project success.
- Supporting cross-functional teams and collaborating with clients to deliver high-quality results
- Leading the development of complex data analysis and reporting solutions
- Generating and validating SDTM and ADaM datasets/analysis files, and tables, listings, and figures (TLFs)
- Producing and QC/validation programming
- Creating and reviewing submission documents and eCRTs
Key responsibilities include:
- Developing and implementing data manipulation and analysis strategies
- Collaborating with cross-functional teams to ensure timely delivery of project milestones
- Providing expert-level guidance on data quality and integrity
- Communicating technical information to non-technical stakeholders
- Participating in ongoing process improvement initiatives
To be successful in this role, you will require:
- 7+ years of experience in a pharmaceutical or biotech company as a Statistical Programmer with a Bachelor's degree or equivalent
- Strong SAS data manipulation, analysis and reporting skills
- Solid experience implementing the latest CDISC SDTM / ADaM standards
- Good ad-hoc reporting skills
- Proficiency in Efficacy analysis
- Submissions experience utilizing define.xml and other submission documents
In return for your expertise, we offer:
- A competitive salary package
- Ongoing training and development opportunities
- Flexible working arrangements
- A collaborative and supportive team environment
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