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7 days ago
Job Title: Data Science and Clinical Trials Professional
">As a senior member of our team, you will play a key role in the success of our clients' clinical trials. You will leverage your advanced programming skills to analyze and report on large datasets, utilizing industry-leading tools such as SAS.
Responsibilities include:
- Designing and implementing data manipulation, analysis, and reporting strategies for clinical trials.
- Generating and validating SDTM and ADaM datasets/analysis files, and tables, listings, and figures (TLFs).
- Production and QC/validation programming.
- Generating complex ad-hoc reports utilizing raw data.
- Applying strong understanding/experience of efficacy analysis.
- Creating and reviewing submission documents and eCRTs.
You will be working closely with cross-functional teams and clients to deliver project specifications, status, issues or inquiries.
Requirements:
- Bachelor's degree in Statistics, Computer Science, Mathematics, etc.
- At least 7 years of SAS programming experience working with clinical trial data in the Pharmaceutical & Biotech industry.
- Study lead experience, preferably juggling multiple projects simultaneously.
- 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.
Our ideal candidate has excellent analytical and troubleshooting skills, with the ability to provide quality output and deliverables under challenging timelines.
If you have experience working in a globally dispersed team environment with cross-cultural partners, this could be the perfect opportunity for you.
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