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Statistician

Req #: 1800472
Location: Berkeley Heights, NJ US
Job Category: General
Work Location: 200 Connell Drive BERKELEY-200 7922
Organization:
Schedule: 0
Shift:
Employee Status: Full time
Job Type: Regular
Job Level:
Travel:
Other Locations:US- NJ- Berkeley Heights- 200

Description

Celgene is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that will change the course of human health.  We value our passion for patients, ​quest for innovation, spirit of independence and love of challenge. With a presence in more than 70 countries, and growing - we look for talented people to grow our business, advance our science and contribute to our unique culture.

Duties:  Provide statistical support to Celgene’s Clinical R&D Department. Contribute to efficient study design, prepare statistical consideration sections and provide input into other protocol sections.  Prepare statistical analysis plans including table shells.  Analyze clinical trial data, and work with programmers to provide tables, listings and graphs, including ad hoc validation.  Review, synthesize, interpret and report analysis results.  Provide ad hoc data driven analyses.  Provide statistical input for the preparation of final study reports and other required documents.  Support preparation of manuscripts.  Provide statistical support for integrated reports, submissions preparation, and post-submission activities.  Escalate issues to functional management as necessary.  Provide continuous feedback to peers and leaders.  Proactively seek ways to gain broader experience/perspectives and focuses on a robust professional development plan. 

Requirements: Master’s degree in Statistics with at least 2 years clinical drug development experience.  Alternatively accepting a Ph.D. in Statistics.  Position requires:   

3 months of applied statistical research experience in the pharmaceutical research industry (e.g., internship or full-time employment) OR academic research centers; Proficiency in SAS programming (Base and Stat Procedures); Experience with MS Office products (Word, Excel, PowerPoint); Demonstrated competency in utilizing various statistical methodologies for trial design and data analysis; Knowledge of and application of clinical trial design concepts, including ability to research clinical trial design options in a time-efficient manner, using both statistical theory and computer simulations, to understand the operating characteristics of these design options, and fully vet in a statistically rigorous manner; Good interpersonal, communication, writing and organizational skills, with the ability to present technical findings and reports to stakeholders; Work in a team environment with medical personnel, clinical monitors, data managers, programmers and medical writers.  

CONTACT: Apply at www.celgene.com and search for REQ ID.

Celgene is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Celgene complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must have authorization to work for Celgene in the U.S.
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About Celgene

Celgene is a global biopharmaceutical company committed to improving the lives of patients worldwide. At Celgene, we seek to deliver truly innovative and life-changing treatments for our patients.

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