| REQUIREMENT # 12-00215 RECRUITER: MICHELLE ASHEN JOB LOCATION: BEDMINSTER, NJ MARCH 15, 2012 Project Description: - Performs QA/QC of Tables, Listings & Graphs (TLGs), CSRs/Manuscripts/DFUs and SAS code to ensure the production of high quality statistical outputs in a timely fashion. Works independently or in collaboration with a QC Stat Programmer.
- Maintain complete and auditable documentation of all programming activities.
- Assist in the development, review and modification of department Standard Operating Procedures (SOP).
- Maintain BDMP calendar of QC deliverables.
- Perform general duties as required to support company objectives.
Required Skills: - Bachelor's degree and SAS programming knowledge, including a minimum of two to four years directly related experience and/or training required.
- Excellent communication skills and project planning experience a must.
- Experience in the design and development of databases to support clinical studies is helpful.
- Knowledge of FDA regulations regarding data quality and Clinical Trials conduct.
- Excellent inter-personal skills.
- Ability to be flexible in changing daily workload priorities as directed.
- Ability to utilize computer reference material to conduct independent research and solve problems.
- Ability to handle stressful situations and deadlines.
- Ability to manage competing priorities in a frequently changing environment.
- Ability to work productively in a team environment.
This 12+ month position starts ASAP. Please E-MAIL your resume (attachment to email) with rate and availability to Michelle: michellea@alphaconsulting.com |
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