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Senior, Biostatistician

EXTRA HOLIDAYS - EXTRA PARENTAL LEAVE
Remote: 
Full Remote
Contract: 
Salary: 
118 - 158K yearly
Experience: 
Mid-level (2-5 years)
Work from: 

Offer summary

Qualifications:

PhD or equivalent in stats/biostats, Master's with 4+ years exp..

Key responsabilities:

  • Serve as trial statistician
  • Develop protocol/SAP
  • Participate in database design
  • Analyze and interpret trial data
  • Prepare reports and provide statistical input
BeiGene logo
BeiGene Biotech: Biology + Technology XLarge http://www.beigene.com/
5001 - 10000 Employees
See more BeiGene offers

Job description

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Your missions

BeiGene continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.

General Description:

The Senior Biostatistician will perform scientific statistical analyses in support of clinical trials with guidance and mentoring on new and complex issues. The position will work with the clinical and regulatory team in designing clinical trials and developing the statistical analysis plan, facilitate the implementation of statistical analyses, provide statistical input to the CSR and scientific presentations/manuscripts. The individual will interface with clinical therapeutic area members, SAS programming, clinical data management, clinical operation, clinical pharmacology, medical writing and other functions. This position will also participate in managing vendors to ensure quality of all deliverables and adherence to requirements/timeline.

The position can be remote, with preference for the selected candidate to be near one of the BeiGene offices in California, Massachusetts, Maryland, or New Jersey.

Essential Functions of the job:

  • Responsibilities will include, but are not limited to, the following:
  • Serve as trial statistician and work in the cross-functional team for study planning and execution, and reporting.
  • Develop individual protocol/SAP and determine appropriate statistical methodology.
  • Participate in database design meetings to ensure that the data collected are in high quality and satisfy analysis requirements.
  • Collaborate with the statistical programming staff to ensure that all programs meet analysis and external requirements. Work with programmers to provide tables, listings and graphs, including ad hoc validation.
  • Analyze data and interprets results from clinical trials to meet objective of the study protocol. Independently apply and implement basic and complex statistical techniques to these analyses. Conduct ad hoc analyses if applicable
  • Prepare oral and written reports to effectively communicate results of clinical trials to the project team and corresponding parties.
  • Provide statistical input through the planning and conduct of clinical trials with departments with BeiGene as well as with external vendor.
  • Make recommendations or resolve technical, quality, and timeline issues.
  • Participate in innovative statistical methodology development that stemmed from project questions.

Supervisory Responsibilities:  

  • No

Computer Skills: R, SAS  

Education Required:

PhD or equivalent degree in statistics/biostatistics or related discipline

Master’s degree with a minimum of 4+ years relevant work experience

Travel:  < 10%

BeiGene Global Competencies

When we exhibit our values of Patients First, Collaborative Spirit, Bold Ingenuity and Driving Excellence, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.

  • Fosters Teamwork
  • Provides and Solicits Honest and Actionable Feedback
  • Self-Awareness
  • Acts Inclusively
  • Demonstrates Initiative
  • Entrepreneurial Mindset
  • Continuous Learning
  • Embraces Change
  • Results-Oriented
  • Analytical Thinking/Data Analysis
  • Financial Excellence
  • Communicates with Clarity

Salary Range: $118,300.00 - $158,300.00 annually

BeiGene is committed to fair and equitable compensation practices. Actual compensation packages are determined by several factors that are unique to each candidate, including but not limited to job-related skills, depth of experience, certifications, relevant education or training, and specific work location. Packages may vary by location due to differences in the cost of labor. The recruiter can share more about the specific salary range for a preferred location during the hiring process.  Please note that the listed range reflects the base salary or hourly range only. Non-Commercial roles are eligible to participate in the annual bonus plan, and Commercial roles are eligible to participate in an incentive compensation plan. All Company employees have the opportunity to own shares of BeiGene Ltd. stock because all employees are eligible for discretionary equity awards and to voluntarily participate in the Employee Stock Purchase Plan. The Company has a comprehensive benefits package that includes Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness.

We are proud to be an equal opportunity employer and we value diversity. BeiGene does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need.

Required profile

Experience

Level of experience: Mid-level (2-5 years)
Industry :
Biotech: Biology + Technology
Spoken language(s):
Check out the description to know which languages are mandatory.

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