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Advanced Clinical Data Analyst
3 weeks ago
Sponsor-dedicated:
You'll be embedded within a global pharmaceutical client, working closely with Cytel's support team. This is an exciting time to contribute to their innovation.
Position Overview:
Leverage your advanced SAS programming skills and CDISC standards proficiency (SDTM & ADaM) to support or lead Phase I-IV clinical trials. This role offers full remote work capabilities.
Our Values
- We apply scientific rigor to unlock data potential.
- We foster intellectual curiosity and enthusiasm for discovery.
- We value collaboration and diverse perspectives.
- We drive innovation with leading-edge technology.
Responsibilities
You will:
- Manipulate, analyze, and report clinical trial data using SAS programming.
- Generate and validate SDTM and ADaM datasets/analysis files, tables, listings, and figures.
- Develop production and QC/validation programming.
- Create complex ad-hoc reports from raw data.
- Apply strong understanding/experience of Efficacy analysis.
- Review and create submission documents and eCRTs.
- Communicate with internal teams and clients for project specifications, status, issues, or inquiries.
- Perform lead duties when needed.
- Work as a team player, adapting to changing priorities.
Qualifications
To succeed in this position, you'll need:
- A Bachelor's degree in Statistics, Computer Science, Mathematics, or related field.
- At least 7 years of SAS programming experience with clinical trial data in the Pharmaceutical & Biotech industry.
- Study lead experience, preferably managing multiple projects simultaneously.
- Strong SAS data manipulation, analysis, and reporting skills.
- Experience implementing CDISC SDTM / ADaM standards.
- QC/validation skills.
- Good ad-hoc reporting skills.
- Efficacy analysis proficiency.
- Familiarity with the drug development life cycle and clinical trials' data manipulation, analysis, and reporting.
- Submissions experience using define.xml and other submission documents.