Senior Biostatistician

Posted Yesterday
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Hiring Remotely in Raleigh, NC, USA
In-Office or Remote
Senior level
Pharmaceutical
The Role
Lead biostatistical design and analysis for clinical studies: develop and review analysis plans, execute complex analyses (SAS/R), QC deliverables, author reports, advise clients, and mentor junior staff.
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.

As an experienced Biostatistician, you will lead research design and analytical strategies, provide input into protocols, develop and review statistical analysis plans and author/co-author reports, abstracts and manuscripts. You will use your knowledge to advise, provide guidance and to oversee the quality control of statistical deliverables. As the functional lead within a study team, you will direct the Biostatistical activities on a study and be accountable for the deliverables.
Our Biostatisticians are not only focused on delivering quality results for our client’s needs, but also value working with one another. Our virtual resources support our teams to work collaboratively and effectively across the globe. The overall long tenure of our team integrates a depth of knowledge and experience. Working together, you will create paths to answers and contribute to new therapies which ultimately will impact the patient. 
What you’ll do...
Supervise, advise and review:

  • Leverage your expertise. Develop complex analysis strategies and execute them using efficient programming techniques (software: SAS, R).

  • Foster teamwork. Perform intricate statistical analyses and provide input to statistical reports. 

  • Share knowledge. Provide input to analysis plans, statistical reports, statistical sections of integrated clinical reports.

  • Impact the process. Be a proactive advisor for all types of analysis from the proposal process through the project life cycle.

  • Take quality seriously. Review analysis data sets and quality control all types of statistical analysis deliverables.

  • Coach and mentor. Train and uplift junior members of the department.

Cooperate and network:

  • Build relationships. Liaise with other biostatistical and company departments to optimize global efficiency.

  • Work collaboratively. Coordinate Biostatistics related project activities for successful completion within given timelines and budget.

  • Interact with heart. Coordinate with clients with regard to data analysis, scope of work, and budget.

  • Demonstrate our expertise. Represent Parexel at client meetings.

More about you...
On your first day we’ll expect you to have:
Experience:

  • A minimum of 4 years industry (or directly relevant) experience 

  • A thorough understanding of the statistical aspects of clinical trials and/or observational studies

  • Experience in statistical analysis in a clinically related subject, within clinical trials

  • SAS programming or R programming skills (desired)

Education:

  • A Masters or Ph.D. level education in biostatistics, statistics, mathematics, or another relevant discipline 

Skills:

  • Confidence, be self-reliant and a quick learner who enjoys working in a matrixed team

  • Good leadership skills

  • Strong oral and written English communication skills

  • A strong work ethic to promote the development of life changing treatments for patients

Skills Required

  • Minimum of 4 years industry or directly relevant experience
  • Thorough understanding of statistical aspects of clinical trials and/or observational studies
  • Experience in statistical analysis in a clinical trials context
  • SAS programming or R programming skills
  • Masters or Ph.D. in biostatistics, statistics, mathematics, or related discipline
  • Ability to review analysis datasets and quality control statistical deliverables
  • Leadership skills and experience supervising or mentoring junior staff
  • Strong oral and written English communication skills
  • Self-reliant, quick learner, able to work effectively in a matrixed/global team

Parexel Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Parexel and has not been reviewed or approved by Parexel.

  • Healthcare Strength Health coverage is described as comprehensive, including medical, dental, vision, HSA/FSA options, and company-paid disability insurance. Descriptions often portray the package as strong or “top notch,” adding meaningful value.
  • Retirement Support Retirement offerings include a 401(k) with company matching and, in some regions, generous pension contributions. Core financial protections are emphasized as a solid part of the total rewards.
  • Leave & Time Off Breadth Time-off programs include ample PTO or flexible/unlimited RTO alongside flexible schedules and remote/hybrid options. Work-life balance support from managers is highlighted as a practical advantage.

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The Company
HQ: Raleigh, NC
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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