When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
Key Accountabilities:
- Assist with the development of statistical analysis plans, mock shells, and programming specifications.
- Under supervision, performing data review and statistical analysis.
- Plan and execute production, validation and documentation of programs for TFLs, analysis datasets and transfers of data for internal and external Customers.
- Perform quality checks, consistency reviews, statistical reviewes of analysis datasets and TFLs.
- Assist in providing inputs to data management staff on database design, validation checks and critical data.
- Assist lead biostatistician in fulfilling project responsibilities.
Business Impact for Organization
- Provide project related assistance for assigned project(s).
- Meet quality and timeline
Skills:
- Good SAS programming skills.
- Knowledge of Windows application.
- Strong oral and written communication skills (including the ability to communicate statistical concepts and information to non-statisticians).
- Knowledge of SDTM / ADaM
Behavioral Competency:
- Professional attitude, Self-motivated, Logical Thinking, Attention to detail.
Education:
- Master's degree in Statistical science preferred or equivalent combination of education and training.
- PhD in Statistics or related discipline is preferred
- Base SAS, SAS/MACROS, SAS/GRAPH, SAS/STAT and CDISC knowledge preferred.
- Experience in Early Phase studies
Language Skills:
- Fluent in English (speak, read, write).
Minimum Work Experience:
- 3 to 5 years of experience
Top Skills
What We Do
Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help life-saving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory and therapeutic expertise, our team of more than 21,000 global professionals collaborates with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. Our depth of industry knowledge and strong track record gained over the past 40 years is moving the industry forward and advancing clinical research in healthcare’s most complex areas, while our innovation ecosystem offers the best solutions to make every phase of the clinical trial process more efficient. With the people, insight and focus on operational excellence, we work With HeartTM every day to treat patients with dignity and continuously learn from their experiences, so every trial makes a difference. For more information, visit parexel.com.
Community Guidelines
Because Parexel’s social media channels are open to the general public and employees, we are not responsible for views expressed other than our own. However, we do not tolerate posts that are:
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• Defamatory, offensive, obscene, vulgar or depicting violence.
• Hateful targeting by race/ethnicity, age, color, creed, religion, gender,
sexual preference or orientation, nationality or political beliefs.
• Sexually explicit or pornographic.
• Fraudulent, deceptive, libelous, misleading or unlawful.
• Referencing criminal or illegal activity.
• Spamming.
We reserve the right to remove any comments that do not adhere to our guidelines as well as report users who violate the rules of our page.







