Grifols

Intern – Statistical Programming

14 March 2024
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Deadline date:
£100000 - £50000

Job Description

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Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.

Statistical Programming Summer Intern Primary Responsibilities:

  •  Generates and validates statistical analyses (tables, listings, and figures) using SAS and other software. Reviews the statistical deliverables, ensures the quality of the deliverables, and acts as an integral member of a clinical project team. 
  • Interacts regularly with other team members within clinical development department or in other departments, preventing potential issues and/or reconciling if issues occur.
  • Maintains overall awareness in the field of statistical programming by self-training. Maintaining current professional knowledge in broad range of clinical research.
  • Performs validation and quality review of deliverables provided by internal or external resources.
  • Supports the Regulatory Affairs with electronic submission to FDA by preparing the submission documents under CRT folder with compliance to eCTD guidelines.
  • May review the programming and data management related documents, e.g., case report form(CRF) design, Annotation of CRF, edit checks, database structure.

 

Requirements:

Knowledge of statistical methodology, including experimental design, linear models, categorical data techniques, nonparametric statistics, and survival analysis.  Knowledge of FDA guidelines related to trial design, analysis, and reporting. Solid skills in computer programming (especially SAS). Strong communication and interpersonal skills. Excellent writing ability to author reports that will be acceptable to regulatory agencies. Strong analytical, problem-solving, and active learning skills.  Strong organizational, documentation, and information gathering skills.  Ability to work in multiple therapeutic indications and able to handle multiple projects across these therapeutic areas.

 

Education Requirement: 

  • Currently pursuing 4 year degree in statistics or related field or Masters/PhD student in statistics or related field
  • Candidate must maintain GPA of 3.0 or higher

 

Third Party Agency and Recruiter Notice:

Agencies that present a candidate to Grifols must have an active, nonexpired, Grifols Agency Master Services Agreement with the Grifols Talent Acquisition Department. Additionally, agencies may only submit candidates to positions that they have been engaged to work on by a Grifols Recruiter. All resumes must be sent to a Grifols Recruiter under these terms or they will be considered a Grifols candidate.

 

Grifols provides equal employment opportunities to applicants and employees without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other characteristic or status protected by law.  We will consider for employment all qualified Applicants, including those with Criminal Histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance.

 

Location: NORTH AMERICA : USA : NC-RTP:USNC0001 – RTP NC-Headquarters 

 

Learn more about Grifols