SAS Programmer (Clinical Studies)

Frazer, PA

Posted: 03/20/2019 Job Number: JN -032019-10561
SAS Programmer (Clinical Studies):

SRG offers flexible staffing solutions with a national presence. We provide contract, contract-to-hire, direct hire and executive search services. SRG utilizes an innovative approach to identify and qualify talent that is unique to the Staffing industry, featuring a cutting-edge platform that allows us to rapidly and precisely match professionals to client requirements. We have a proprietary database of over one million candidates and maintain continuous contact with our qualified talent.
  • Title: SAS Programmer (Clinical Studies)
  • Location: Frazer, PA
  • Industry: Pharmaceutical
  • Hours: Monday-Friday; 8:00 am 5:00 pm
  • Salary: $55.00 hour-$60.00 hour paid weekly with benefits options
  • Employment Type: Contract 1 year with possible extension or conversion
Environment: This client is a worldwide leading generic pharmaceutical company and one of the top 15 companies in the industry. With over 45,000 employees in 60 countries worldwide, they are proud to say that our employees are the reason for our success . They believe in empowering employees, presenting them with new challenges and letting them grow and develop professionally. Isn t this the type of company you want to work for?

Job Scope: This position is responsible to provide high level skills of clinical programming support of clinical projects and regulatory submissions. The Senior SAS Programmer is playing a lead role generating and validating analysis datasets, tables, listings and figures.
  • Develop and validate SAS programs of derived datasets
  • Develop and validate SAS programs that create accurate data displays and outputs
  • Develop and validate SAS programs for integrated datasets from various studies/projects
  • Incorporate data in formats other than SAS into SAS datasets
  • Providing strong programming support to CDISC based e-submission
  • Supports Phase I, II, III and IV clinical studies
  • Support requests related to Pre-Clinical, Medical Affairs and publications
  • Participate in project team meetings
  • Responsible for data submission and eCRT preparation according to regulatory guidelines
  • Participates in the development of global data standards, SDTM, ADaM and database structure
  • Resolve and/or escalate issues in a timely fashion
  • Ensure timely, efficient and high-quality deliverables in all projects
  • Lead/co-lead clinical programming for a study or for a regulatory submission
  • Develop, review, document and perform validation of generic SAS macros
  • Initiate and lead new processes, new methodologies and operational ideas and re-challenge existing ones to improve the services provided, effectiveness and efficiency
  • Taking initiative in improving clinical programming processes with focus on SAS Programming
  • Responsible for providing professional expertise and leadership through leading departmental tasks
  • Supervise and support outsourcing activities
Skills Needed:
  • Bachelor's or higher degree in Science, Statistics, Information Technology
  • 3+ years of professional experience in a pharmaceutical or clinical research setting as a programmer
  • Experience in SDTM and ADaM, acquainted with CDISC guidelines and requirements
  • In-depth SAS Programming knowledge
  • Understanding of clinical data and pharmaceutical development
EOE/ADA

SAS Programmer, SAS, SDTM, ADaM , CDISC, Clinical Studies, Clinical Research, Clinical, Clinical Project, FDA, Pharmaceutical
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