Senior Statistical Programmer

Reposted 5 Days Ago
Be an Early Applicant
Taipei City, TWN
In-Office
Senior level
Pharmaceutical
The Role
Lead and coordinate statistical programming teams to produce and QC SDTM/ADaM datasets, tables, figures, and listings; manage project timelines, budgets, regulatory documentation, and stakeholder interactions while ensuring compliance with SOPs, ICH-GCP, CDISC, and other regulations.
Summary Generated by Built In

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:

  • Act as the R Statistical Programming Lead for assigned studies or projects.

  • Contribute to the planning and negotiation of statistical programming timelines and ensure deliverables are completed on schedule.

  • Coordinate and support a statistical programming team to deliver high-quality outputs within timelines and budget.

  • Monitor project progress, resource allocation, and identify potential scope changes.

  • Support project start-up activities including development of R programming frameworks, reusable scripts, and tracking tools.

  • Review statistical analysis plans (SAPs), mock shells, and database specifications to ensure programming feasibility.

  • Collaborate with sponsors and cross-functional teams on statistical programming strategies and technical issues.

  • Proficiency in R and ability to learn new systems and function in an evolving technical environment.

Top Skills

21 Cfr Part 11
Adam
Cdisc
Electronic Submissions
SAS
Sdtm
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The Company
HQ: Durham, North Carolina
20,524 Employees

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: • Abusive, harassing or threatening to others. • 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.

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