Clinical SAS Programmers Job in Research Triangle Park, North Carolina US
If you’re interested in working for a Leading, Mid-Size Contract Research Organization (CRO) that has a massive global reach, then look no further, because Pharm-Olam International offers all of that and more! We are a company that strives to deliver cost-effective, quick-to-market clinical services in today’s emerging marketplace. Pharm-Olam International has one of the largest global footprints of any CRO today and we are committed to not only maintain our standard, but to continue to strengthen our presence even further!
We are currently seeking EXPERIENCED PROFESSIONAL candidates to fill the role of a
**Clinical SAS Programmer**
Such candidates would play a vital role in writing programming needed to generate tables and listings for clinical data on assigned projects. You will definitely feel a sense of involvement working at this SAS Programmer level and the position will challenge you to put your programming skills to use! Don't let this exciting opportunity pass by!
Plus, we have a unique global team culture that offers a competitive salary and amazing benefits package!
Position:
We are currently seeking three qualified Clinical SAS Programmers. These are full-time office based positions located in either Houston, Texas; Research Triangle Park, North Carolina; or Plainsboro, New Jersey. The preferred location is Houston, Texas based on position training needs. Relocation is NOT provided for this position.
Main Function:
SAS Programmers would be responsible for creating, modifying and maintaining programs, primarily in SAS, in efforts of supporting the clinical data management department. This includes, but is not limited to: “Manual” Data Quality Checks (DQC), Data Review Listings, Data Extracts, Data Mapping from and Importing External Data Files (EDF).
Such candidates would have to help design data review specifications. They would need to manage and manipulate multiple large (SAS) data sets, including, but not limited to: defining data, reviewing data sets and variables, performing calculations and providing summarizations. This role also requires candidates to prepare specific data review deliverables and combine multiple data sets needed to create cohesive data review reports that would meet project team and/or client specifications.
Skills/Qualifications:
- Bachelor’s Degree in a Related Field
- Minimum of 4 plus years of (SAS) programming experience preferably within the CRO industry
- Pharmaceutical/clinical research experience required
- Experience in the maintaining and supporting of Data Management processes in a distributed client base within a regulated environment
- Thorough understanding of GCPs, ICH Guidelines and CFR (Thorough understanding of assigned protocols
- Good understanding of the clinical, data management and statistics processes including terms and practices of the field
- Good understanding of System Life Cycle process and applicable GCP regulations pertaining to computer systems, in particular 21 CFR Part 11
- Advanced computer skills, particularly with MS Word, Excel and the Internet
- High degree of analysis and problem solving skills
- Excellent English, verbal and written communication skills required
- Good organizational and time management skills; must be able to establish priorities and able to multi-task
- Good business acumen with customer focus in interacting with peers, sites and clients
For Consideration:
Please forward resume and salary requirements for confidential consideration via email to desiree.futrell@pharm-olam.com or fax to (832) 202-0564. Due to the number of inquiries, we are unable to respond to each inquiry. Candidates of interest, matching the above qualifications will be contacted for further consideration.
PRINCIPALS ONLY, NO PHONE CALLS PLEASE.