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:
Operational Execution
- Production and/or QC of derived datasets and both simple and advanced statistical outputs using efficient programming techniques
- Understand and apply moderately advanced statistical methods
- Coordinate and lead a project team to successful completion of a project within given timelines and budget
- Interact with clients as key contact with regard to statistical and contractual issues
- Assist in the production of analysis plans, statistical reports, statistical sections of integrated clinical reports and other process supporting documents
- Check own work in an ongoing manner to ensure first-time quality
- Provide training in statistical analysis to internal clients
- Proactively participate in and/or lead process/quality improvement initiatives
- Travel to, attend and actively contribute to all kind of client meetings as appropriate (eg discussing analysis concepts, presenting and discussing study results
General Activities
- Mentor and train junior members of the department
- Additional responsibilities as defined by supervisor/manager
Business Development
- Support of Business Development, eg by attending and preparing bid defense meetings
Skills:
- Good analytical skills
- Good project management skills
- Professional attitude
- Attention to detail
- A good understanding of statistical issues in clinical trials
- Prior experience with SAS programming desirable
- Ability to work independently
- Good mentoring/leadership skills
Knowledge and Experience:
- PhD in Statistics or related discipline entry level, MS in Statistics or related discipline with some experience
- The knowledge of pharmacokinetic data is an advantage
- Competent in written and oral English in addition to local language
Education:
- PhD in Statistics or related discipline, MS in Statistics or related discipline
Skills Required
- PhD in Statistics or related discipline or MS in Statistics with some experience
- Prior experience with SAS programming
- Good analytical skills
- Good project management skills
- Attention to detail
- Understanding of statistical issues in clinical trials
- Mentoring and leadership skills
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.
Parexel Insights
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.
