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Apply online for the
Senior/Principal Programmer Analyst/Mgmr, Programming - Oncology
position and advance your career in the
Pharmaceutical industry today.
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Senior/Principal Programmer Analyst/Mgmr, Programming - Oncology : GlaxoSmithKline
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| Job Number |
56245 |
| Employee Type |
Full Time |
| Company Name |
GlaxoSmithKline |
| Location |
Collegeville
Pennsylvania
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| Salary (year) |
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| Experience |
2 to 5 Years |
| Start Date |
1/4/2010 |
| Industry |
Pharmaceutical |
| Job Type |
Clinical |
| Relocation |
Not Required |
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| Description |
Basic Qualification
Bachelors degree or equivalent experience in Statistics, Computer Science, Operations Research, or related discipline.
- Minimum of 4 years experience in the pharmaceutical industry, with at least 3 years experience in analyzing and reporting clinical trials.
- Excellent SAS programming skills including Base SAS, SAS Macro and SAS Graph.
- Good understanding of the drug development process.
- Excellent interpersonal, verbal and written communication skills.
- Demonstrated ability to work across international and functional boundaries.
- Experience in Clinical Pharmacology and knowledge of pharmacokinetic (PK) data a plus.
- Knowledge of Software Development Lifecycle a plus.
For C5: all of the above plus minimum of 9 years experience in the pharmaceutical industry.
Details
In this role as Principal/Senior Programmer/Analyst within the Clinical Pharmacology Data Sciences department the successful candidate will be expected to :
- Work on clinical projects to provide technical input to study teams, create analysis-ready data sets and data displays; creation of Population PK data sets.
- Work closely with statisticians and data managers, but should be able to work independently to perform and coordinate programming duties.
- Act as a department point of contact for customers in Clinical Pharmacology, clinical study teams, and across other departments in Biomedical Data Sciences (BDS) and attend meetings with senior staff within these groups as appropriate.
- Provide input and expertise into and participate in process improvement initiatives and system development projects.
- Work with staff in the other internal departments and outsourced operations to help review and prioritize workload.
- Act as coordinator and contact for outsourced programming and reporting work.
- Develop and provide programming and reporting training to staff.
- Be able to act as a mentor or supervisor for more junior and contract staff.
- Ensure high quality for all programming and reporting
For C5 Manager: all of the above plus…
-Posess project and matrix management skills in order to lead/facilitate a cross-functional group. Possess high-level cross functional and business knowledge.
-Posess ability to lead both project and non-project activities concurrently.
-Lead in Planning complex cross-functional projects.
-Ability to evaluate strategic partnerships and influence contract negotiations.
-Ability to manage permanent staff and cover for Line Manager in their absence
When applying for the above opportunity please use the ‘Cover Letter ‘ of the on-line application to describe how you meet the requirements for this role. |
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| Requirements |
Preferred Qualification
Masters degree preferred. Experience in Clinical Pharmacology and Oncology therapeutic areas preferred. |
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| Contact Info |
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Apply online at company website |
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