Description
Duties:- Uses professional concepts and company's policies and procedures to solve a wide range of difficult problems in imaginative and practical ways to support lead programmer in generation of analysis datasets, generation of TLGs (Tables, Listings, and Graphs), validation of aforementioned data and reports, and maintenance of study documentation
- Other ad hoc tasks as assigned
Work Experience:
- 2-5 years related experience.
- Experience is within the pharmaceutical/biotech industry or relevant clinical research organization Industry.
- Experience in programming with a regulated environment.
Management of Staff:
- There is no management of staff for this level
Functional/Technical Knowledge & Skills (including any required proficiency for particular computer programs or applications, if applicable):
- A knowledge of SAS System Software not limited to but must meet at a minimum
Customer & Industry Knowledge:
- Previous knowledge should be in the pharmaceutical/biotech industry clinical research organization Industry.
- Oncology experience a plus, especially efficacy
- Basic knowledge with the drug development process
- Basic knowledge of ICH, FDA, and GCP regulations and guidelines
- Basic knowledge of CDISC/SDTM and ADaM standards a plus
Education/Training:
- BS/BA/MS in Statistics, Computer Sciences, Mathematics, or Life Sciences, or equivalent experience.
License/Certification Required:
- Although not required a SAS Certification in Base Programmer or Advanced Programmer could be used to support a working knowledge of SAS System Software.
ADDITIONAL REQUIREMENTS:
- Strong communication skills (verbal and written)
- "can do" attitude
- commitment to teamwork
- takes initiave
- Uses rigorous logic and methods to solve difficult problems with effective solutions; can see hidden problems.
To find out more about Real please visit www.realstaffing.com