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Difference between revisions of "Sr. Clinical SAS Programmer- Home Based"

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Latest revision as of 19:36, 28 January 2018

Note: This employment opportunity has expired and is no longer available. It has been retained for historical interest only.
For current listings see Employment opportunities.



COMPANY: PRA Health Sciences

POSITION: Sr. Clinical SAS Programmer

JOB DURATION: FT/Perm

LOCATION: Home Based

DESCRIPTION: As the Senior Statistical Programmer you will be responsible for the development, quality control and documentation of statistical (SAS) programs in support of department projects. You will need to demonstrate the ability to interpret clinical data and apply analytical techniques to meet the objectives and requirements of clinical studies. In addition, you will exhibit leadership qualities, outstanding SAS programming skills, and a working knowledge of regulatory and clinical research standards.


POSTING EXPIRATION DATE:12/31/2017


REQUIRED SKILLS:

  • Bachelor's Degree in appropriate discipline
  • 5 years pharmaceutical industry based Biostatistics and Programming experience
  • 3 years pharmaceutical industry based experience programming within SAS
  • Oncology experience strongly preferred
  • Knowledge of data structure standards (SDTM, ADaM).
  • Understanding of clinical programming within the tabulation, analysis and reporting of clinical trials.
  • Ability to provide leadership of tabulation, analysis and reporting activities for a clinical trial, including the planning, supervision, implementation and monitoring of clinical programming processes.


RESPONSIBILITIES:

  • Assist in the planning and execution of SAS programming activities for a single project.
  • Assist in the review and input into project requirements.
  • Develop SAS programs in support of clinical trial acivities.
  • Perform quality control in support of clinical trial activities.
  • Maintain documentation as appropriate.
  • Deliver individual programming deliverables of medium to high complexity within a single project.
  • Demonstrate full proficiency in technical/programming skills.
  • Contribute broad knowledge of clinical trial activities.


ADDITIONAL INFORMATION:


CONTACT INFORMATION: Name: Suzanne Curtis

Phone: 434-951-3451

Fax:

E-mail: curtissuzanne@prahs.com

Web site: www.prahs.com