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Analyst Intern

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  • Internship
    Full-time
    Off-cycle Internship
  • Science
    Data
  • San Diego

Requirements

  • Bachelor’s or above degree in statistics/biostatistics or computer sciences.
  • Basic knowledge of Base SAS, including SAS macro language, is preferred. Programming experience in a research environment is a plus.
  • Credits in statistics courses are desired.
  • Understands the sequence of running programs to ensure up-to-date data and to troubleshoot, debug programming problems and to identify data trends.
  • Proficiency in Microsoft Office (Word, Excel, and PowerPoint).
  • Effective verbal and writing skills.
  • Must be able to work in an office environment, which has minimal noise conditions.
  • Ability to stand or sit for most of the work day.
  • Must be able to perform some activities with repetitive motion, such as keyboarding.

Responsibilities

  • Assist CSP members with transforming specifications in statistical analyses plan into fully documented, validated programs supporting both safety and efficacy displays and analysis datasets required for clinical study reports.
  • Assist in testing, maintaining, and documenting programs for use in creating study datasets in standard data tabulation model format, analysis datasets, statistical tables, figures, and listings.
  • Assist Clinical Data Management with creating well-documented validated standard and non-standard edit check and monitoring programs to support the clinical trial team to ensure the integrity, accuracy and completeness of the data in preparation for clinical reporting.
  • Adhere to statistical analysis plans and standard operating procedures while completing routine programming activities.
  • Meet milestones as assigned with high quality.
  • Perform other duties as directed by management or senior programming personnel.

FAQs

What kind of projects will the Analyst Intern be working on?

The Analyst Intern will assist in programming tasks related to clinical trials, including developing databases and statistical programming solutions, creating study datasets, and supporting the integrity and completeness of clinical data.

What educational qualifications are required for this internship?

A Bachelor’s degree or above in statistics/biostatistics or computer sciences is required for this internship.

Is prior programming experience necessary for this role?

While basic knowledge of Base SAS and SAS macro language is preferred, prior programming experience in a research environment is a plus, but not strictly required.

What software skills are necessary for this position?

Proficiency in Microsoft Office applications, particularly Word, Excel, and PowerPoint, is required.

Are there any specific skills that would be advantageous for this role?

Yes, having credits in statistics courses and understanding how to troubleshoot and debug programming issues are beneficial skills for this position.

What type of work environment should the Analyst Intern expect?

The Analyst Intern will work in an office environment with minimal noise, where most activities involve sitting or standing for extended periods and performing repetitive motions like keyboarding.

Will there be opportunities to learn under experienced professionals?

Yes, the Analyst Intern will be working under the direction of the CSP Lead and will assist senior programming personnel, providing opportunities for mentorship and learning.

Is the internship position open to all applicants?

Yes, this position is an Equal Opportunity Employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status.

Are there performance expectations for this role?

Yes, the Analyst Intern is expected to meet assigned milestones with high quality while adhering to statistical analysis plans and standard operating procedures.

Will the Analyst Intern be required to perform other duties?

Yes, the job description states that the Analyst Intern may be required to perform additional job-related duties as requested by management.

The global pharmaceutical and medical device open-access capability and technology platform

Science & Healthcare
Industry
10,001+
Employees
2000
Founded Year

Mission & Purpose

As a global company with operations across Asia, Europe, and North America, WuXi AppTec provides a broad portfolio of R&D and manufacturing services that enable the pharmaceutical and healthcare industry around the world to advance discoveries and deliver groundbreaking treatments to patients. Through its unique business models, WuXi AppTec’s integrated, end-to-end services include chemistry drug CRDMO (Contract Research, Development and Manufacturing Organization), biology discovery, preclinical testing and clinical research services, and cell and gene therapies CTDMO (Contract Testing, Development and Manufacturing Organization), helping customers improve the productivity of advancing healthcare products through cost-effective and efficient solutions. WuXi AppTec received AA ESG rating from MSCI in 2022 and its open-access platform is enabling more than 5,950 customers from over 30 countries to improve the health of those in need – and to realize the vision that "every drug can be made and every disease can be treated."

Culture & Values

  • Integrity & Dedication

  • Working Together & Sharing Success

  • Doing the Right Thing

  • Doing It Right