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.
Name of Employer: Parexel International LLC
Position Title: Principal Statistical Programmer
Position Location: 275 Grove Street, Newton, MA 02466
Hours: Full Time / 40 hours
Summary of Duties: Provide technical support and expert advice to internal and external sponsors on statistical programming projects to support clinical trial activities. Work independently to support various programming activities related to analysis and reporting of clinical study data. Fill the Statistical Programming Lead role on projects and liaise with sponsors, Biostatistics Leads, Data Management Leads, and other functional areas. Monitor quality, timelines, resource allocation, and productivity in relation to budget. Project management for statistical programming. Advise and negotiate statistical programming timelines.
Education requirements: Bachelor’s degree in Statistics, Mathematics, Pharmaceutical Science, Data Analytics or related field of study. Employer will accept post-secondary academic coursework and/or relevant work experience which is evaluated as equivalent to a U.S. Bachelor’s degree in accordance with 8 CFR §214.2(h)(4)(iii)(D).
Experience requirements: 7 years of progressive experience in statistical programming.
Special Skills or Other Requirements: Applicants must have demonstrated experience with:
1) Programming and reporting process.
2) FDA 21 CFR Part 11 regulations;
3) ICH-GCP, CDISC, and WSOP guidelines;
4) Analyzing data from Phase I, II, and III clinical trials;
5) SAS/BASE, SAS/STAT, SAS/SQL, SAS/MACRO, SAS Data Step, Proc Step, and Functions;
6) Generating reports, tables, and listings for statisticians;
7) Building structured, CDISC, SDTM or ADaM databases for clinical studies; and
8) Leading teams in a statistical programming environment.
*100% Remote reporting to Newton, MA.
*Position eligible for Employee Referral Program*
To apply: Individuals interested in applying for the position may email a resume with Job #LV0209 to [email protected].
EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
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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.
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