Clinical SAS Programmer jobs

Job Search

Go to Advanced Search »

The Company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, genetic information or any other characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please call 844 895-8598 or email accommodation@aerotek.com. However, if you have questions about this position, please contact the Recruiter located at the bottom of the job posting. The Recruiter is the sole point of contact for questions about this position.



Clinical SAS Programmer

Company: Aerotek Clinical
Location: San Francisco, California
Category: Clinical Jobs
Rate: $55.00 to $90.00 per Hour
Job Type: Contract-to-Hire
Posting ID: 3089599
Posting Date: 6/11/2014 Allegis Group Family of Hiring Companies

Apply Online for this Job Today

Already a Member?
If you're currently a thingamajob.com member?    Please apply here.
Not a Member?
        

Clinical SAS Programmer Job Description:

A growing pharmaceutical company in the bay area is actively interviewing for an experienced Clinical SAS Programming professional to join their Biometrics team. The clinical programmer will be focused on validating macros and datasets, mentoring junior programmers, and ensuring all data transfers are scheduled and multiple data sources are coordinated. This position reports directly to the Director of Biometrics. Ideal candidates have a minimum of 3 years experience as a clinical SAS programmer working at a sponsor pharmaceutical company.

Scope of responsibilities:
An ability and willingness to gain in-depth knowledge of assigned studies’ protocols, CRFs, clinical and external data structure and content, study timelines and key milestones
-Awareness of Clinical Programming activities needed to support study conduct
-Point person for all study team or management queries about Clinical Programming activities for assigned studies
-Proactively ensure all data transfers are scheduled and multiple data sources coordinated if necessary to support the reporting needs of assigned studies.
-Ensure specifications are in place for all data transfers, verification of data against data transfer specs, reconciliation of external data with clinical data, clinical data review deliverables, including patient profiles and BOXI reports, and study metrics deliverables
-Review routine specifications drafted by support programmers or study team members, revise if needed with input from team
-Gather requirements from study team and write complex specifications for metrics or reports for assigned studies
-Ensure end users have sufficient detail (QC listings, support data presentation) in addition to the formal deliverables to evaluate them for approval
-Manage the Clinical Programming queue of work from request to release
-Send reviewed/completed specifications for programming
-Answer technical questions from programmers, or coordinate with end users for clarifications if needed
-Ensure support programmers (in-house or CRO) meet timelines, or escalate any at risk
-Review programmed output against the specifications
-Coordinate end user review and address any feedback
-Release finalized programming into production
-Provides responsive programming support for any tight-timeline, ad hoc, or crucial deliverables or data transfers, and for quick turnaround code fixes to facilitate release

Qualifications:
Bachelor in Computer Sciences, Mathematics, Life Sciences with a minimum of 5 – 8 years of clinical or statistical (SAS) programming experience in the pharmaceutical or biotechnology industry, or MA/MS with 4 years of experience (less needed for junior candidates)
-Proven Clinical (SAS) Programmer experience in a pharmaceutical or CRO working in a FDA regulated environment
-Excellent verbal/written and interpersonal skills required for working successfully in a cross-functional team environment; communicate and collaborate effectively with cross-functional teams in face-to-face conversation, by telephone, and by email.
-Ability to translate requirements expressed in non-technical language into technical specifications or programming instructions
-Oncology experience preferred
-Experience in EDC systems, data management preferred
-BOXI a plus
-Excel graph skills a plus
-SAS Certification (BASE or ADVANCED) a plus

Required Skills for Clinical SAS Programmer Job:

  • SAS
  • SDTM DATASETS
  • ADAM DATASETS
  • MACROS VALIDATION
  • ONCOLOGY

About Aerotek Clinical:

Join Aerotek Clinical, a division of Aerotek Scientific® LLC, one of the fastest growing providers of scientific and clinical services in the country. Due to our growth, we’re constantly on the lookout for qualified professionals to place in contract, contract-to-hire, and permanent placement positions across a number of different industries. We know it’s more than just your day-to-day responsibilities that can make or break a job. It's the support you get. That's the reason Aerotek offers a variety of benefits including medical, dental, optical, 401k, and many more. Don't put your career in the hands of just anyone, put it in the hands of a specialist. Join the Aerotek team! Allegis Group and its subsidiaries are equal opportunity employers and will consider all applications without regard to race, marital status, sex, age, color, religion, national origin, veteran status, disability or any other characteristic protected by law.

Contact Information

Noelle Louise Vavuris Apply Now! Begin by filling out the "Apply Online for this Job" section at the top of the page Need Directions? Get office driving directions with Google Maps
nvavuris@aerotek.com
Aerotek Clinical - San Francisco, CA
395 Oyster Point Blvd.
Suite 120

S. San Francisco, CA  94080
TEL: ( ) -
TEL: ( ) - x
FAX: ( ) -

We're Hiring

7,800 jobs waiting to be filled!

US Security Clearance Jobs

Recently Viewed Postings