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Senior Statistical Programmer

82% Flex
EXTRA HOLIDAYS - EXTRA PARENTAL LEAVE - FULLY FLEXIBLE
Remote: 
Full Remote
Experience: 
Mid-level (2-5 years)
Work from: 

Offer summary

Qualifications:

Degree in relevant field, Proficient in SAS.

Key responsabilities:

  • Lead statistical programming projects
  • Review and ensure quality of datasets
Parexel logo
Parexel Pharmaceuticals XLarge https://www.parexel.com/
10001 Employees
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Job description

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Your missions

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.

Key Accountabilities:

Project Management:

  • Ability to fill Statistical Programming Lead role on projects

-Input into and negotiate statistical programming timelines. Ensure that timelines are adhered to.
-Coordinate and lead a statistical programming team to successful completion of a study within given timelines and budget.
-Monitor project resourcing, project budgets, and identify changes in scope.

  • Coordinate project start-up activities, creation of global programs, tracking spreadsheets, and other required documentation.

  • Review statistical analysis plans and mock-shells.

  • Review database set-up specifications.

  • Interact with sponsors and internal stakeholders with regard to statistical programming issues.

  • Assist project teams in the resolution of problems encountered in the conduct of their daily work.


Statistical Programming for Assigned Projects:

  • Deliver best value and high quality service.

  • Check own work in an ongoing way to ensure first-time quality.

  • Use efficient programming techniques to produce/QC derived datasets (e.g. SDTM, ADaM), tables, figures, and data listings.

  • Experience with PROC Report

  • Complex SAS Graph programming experience

  • Produce/QC complex ADaM dataset specifications and other process supporting documents and submission documentation.

  • Ensure quality control (QC) is performed on all process and technical activities related to derived dataset, table, data listing, and figure programming in accordance with corporate quality standards, SOPs/Guidelines, ICH-GCP, and/or other international regulatory requirements.

Training:

  • Maintain and expand local and international regulatory knowledge within the clinical industry.

  • Develop knowledge of SAS and processes/procedures within other PAREXEL functional areas.

  • Provide relevant training and mentorship to staff and project teams.

General:

  • Maintain all supporting documentation for studies in accordance with SOPs/Guidelines to ensure traceability and regulatory compliance.

  • Ensure compliance with SOPs/Guidelines, ICH-GCP, and any other applicable local and international regulations, and participate in internal/external audits and regulatory inspections as required.

  • Proactively participate in and/or lead process/quality improvement initiatives.

  • Provide consultancy to internal and external sponsors with regard to statistical programming tasks.

  • Represent PAREXEL at sponsor marketing and technical meetings.

  • Understand regulatory requirements concerning industry technical standards(e.g. CDISC, 21 CFR Part 11, and electronic submissions).

Skills:

  • Excellent analytical skills.

  • Proficiency in SAS.

  • Experience with PROC Report

  • Complex SAS Graph programming experience

  • Extensive knowledge and understanding of the programming and reporting process.

  • Knowledge of SOPs/Guidelines, ICH-GCP, and any other applicable local and international regulations such as 21 CFR Part 11.

  • Ability to learn new systems and function in an evolving technical environment.

  • Strong project management skills.

  • Strong organizational skills, ability to manage competing priorities, and flexibility to change.

  • Attention to detail.

  • Ability to successfully lead a global team.

  • Work effectively in a quality-focused environment.

  • Effective time management in order to meet daily metrics or team objectives.

  • Show commitment to and perform consistently high quality work.

  • Business/operational skills that include customer focus, commitment to quality management, and problem solving.

  • Demonstrate commitment to refine quality processes.

  • Good presentation skills.

  • Good business awareness/business development skills (including financial awareness).

Knowledge and Experience:

  • Competent in written and oral English.

  • Excellent communication skills.


Education:

  • Educated to degree level in a relevant discipline and/or equivalent work experience.

Required profile

Experience

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

Soft Skills

  • Commitment to Quality
  • Effective Communication
  • Analytical Thinking
  • Attention to Detail
  • Leadership
  • Flexibility
  • Adaptability

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