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Senior Biostatistician

extra holidays - extra parental leave - fully flexible
Remote: 
Full Remote
Contract: 
Full time
Experience: 
Senior (5-10 years)
Work from: 
South Africa

Offer summary

Qualifications:

5+ years of industry experience, Masters or Ph.D. in related discipline.

Key responsabilities:

  • Lead research design and analytical strategies
  • Conduct statistical analysis and deliverables oversight
Parexel logo
Parexel XLarge http://www.parexel.com
10001 Employees
About 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 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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Job description

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. Senior and Principal level Biostatisticians at Parexel are client-facing and play an integral part in the study team.

Our Biostatistics teams are not only focused on delivering quality results for our client’s needs, but also value working with one another in a flexible environment. Although some team members are home-based and others are office-based, 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 5 years industry (or directly relevant) experience 

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

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

  • 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

  • The ability to travel as required, although this is not frequent

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

Required profile

Experience

Level of experience: Senior (5-10 years)
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Hard Skills

R (Programming Language)Statistical AnalysisSAS (Software)BiostatisticsEpidemiologyClinical TrialsStatistical ProgrammingData Analysis

Other Skills

  • Teamwork
  • Communication
  • Leadership
  • Problem Solving
Are you interested?

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