Search for Principal Statistical Programmer roles with a focus on remote work, requiring 7+ years of experience, knowledge of SAS, and expertise in clinical trial data analysis, preferably in the biomedical field.

Okay, I've searched for Principal Statistical Programmer roles that focus on remote work, require 7+ years of experience, emphasize SAS expertise, and involve clinical trial data analysis in the biomedical field. I found 42 positions for you.

Principal Statistical Programmer

Remote

7 years + Experience

SAS

Biomedical

Can you help me to analyze the job description and company culture?

Sure. Here's the analysis:

Job Analysis:

The Principal Statistical Programmer at Parexel is fundamentally hired to ensure the integrity and timeliness of statistical programming projects, specifically within the context of clinical trials. This role entails providing technical expertise and leading programming efforts that support the analysis and reporting of clinical study data. The responsibilities include independent execution of programming tasks, cross-functional collaboration with biostatistics and data management teams, and proactive project management to meet quality standards and deadlines. Success in this role is characterized by the ability to manage resources efficiently, ensure adherence to regulatory guidelines, and deliver high-quality programming outputs that facilitate informed decision-making in clinical development. The challenges faced likely stem from the need to navigate complex datasets, adhere to stringent regulatory compliance, and adapt to changing project requirements, all while maintaining effective communication with stakeholders. Achieving high levels of satisfaction and trust from both internal teams and external sponsors will be crucial for the individual in this position.

Company Analysis:

Parexel operates in the clinical research organization (CRO) industry, providing essential support for biopharmaceutical companies in all phases of clinical trials. As one of the largest CROs globally, Parexel is well-positioned to influence the healthcare landscape, especially in advancing innovative treatments. The company’s focus on operational excellence and patient-centric approaches suggests a culture that values efficiency, continuous improvement, and compassion in clinical research. This implies that a Principal Statistical Programmer will thrive in a fast-paced, dynamic environment that prioritizes collaboration across teams. This role likely reports to a statistical programming lead or project manager and may interface directly with higher management, providing visibility and influence within the organization. Importantly, the team's efforts align with Parexel's mission to expedite the delivery of life-saving treatments, reinforcing the strategic importance of the statistical programming team in achieving corporate goals. The position is indicative of a strategic hire aimed at bolstering project management capabilities in statistical programming, thus aiding Parexel's goal of enhancing trial access and efficacy worldwide.

Mock up some interview questions based on the job description.

Absolutely. Here are some mock interview questions that could come up:

Tell me about a time when you had to manage tight deadlines for statistical programming. How did you prioritize your workload?
Describe your experience with FDA 21 CFR Part 11 regulations. Can you provide an example of how you ensured compliance in your previous projects?
How have you handled disagreements or conflicts with team members or stakeholders in past projects?
What was one of the most challenging statistical programming projects you worked on? What role did you play, and what was the outcome?
How would you approach the programming and reporting process for a clinical trial involving both Phase I and II components?
Can you discuss your experience with generating CDISC datasets and the importance of adherence to those standards?
Describe a complex dataset you have worked with. What tools did you use to analyze it, and how did you ensure the data's reliability?
Imagine you are leading a programming team and have received new project requirements that conflict with prior timelines. How would you manage the expectations of your team and the stakeholders?
If you discovered a significant error in the programming results just before a deadline, what steps would you take to address it?
Why are you interested in working specifically for Parexel and what about our mission resonates with you?
How do you think your experience in statistical programming aligns with our focus on patient-centric clinical trials?
What are some challenges you foresee in statistical programming for clinical trials, and how might you address them in this role?
Do you have any questions about the team structure or how the statistical programming team collaborates with other departments?
What are your thoughts on the importance of operational excellence in clinical research, and how have you demonstrated this in your career?
What strategies do you employ to stay current with regulatory changes in the clinical research sector?

Job Details

Overview Company

Principal Statistical Programmer

Parexel

2 days ago

Highlight

RemoteFull-time7+ yearsSenior

Summary

Parexel International LLC is seeking a Principal Statistical Programmer to join their team in Newton, MA. The role involves providing technical support and expert advice on statistical programming projects to support clinical trial activities.

About the Role

As a Principal Statistical Programmer, you will work independently to support various programming activities related to analysis and reporting of clinical study data. You will fill the Statistical Programming Lead role on projects, liaise with sponsors, Biostatistics Leads, Data Management Leads, and other functional areas. Responsibilities include monitoring quality, timelines, resource allocation, and productivity in relation to budget, project management for statistical programming, and advising and negotiating statistical programming timelines.

About You

Required:

Bachelor’s degree in Statistics, Mathematics, Pharmaceutical Science, Data Analytics or related field of study or equivalent experience.
7 years of progressive experience in statistical programming.
Demonstrated experience with programming and reporting process, FDA 21 CFR Part 11 regulations, ICH-GCP, CDISC, and WSOP guidelines.
Experience analyzing data from Phase I, II, and III clinical trials.
Proficiency in SAS/BASE, SAS/STAT, SAS/SQL, SAS/MACRO, SAS Data Step, Proc Step, and Functions.
Experience generating reports, tables, and listings for statisticians.
Experience building structured, CDISC, SDTM or ADaM databases for clinical studies.
Experience leading teams in a statistical programming environment.

Parexel

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 24,000 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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Newton, MA