Senior Programmer Analyst Job in Los Angeles, California Us


Cougar Biotechnology, Inc., a Johnson Johnson company, with a specific focus on the field of Oncology, is recruiting for a Senior Programmer Analyst, located in Los Angeles, CA.

Cougar's oncology portfolio includes Abiraterone Acetate (Zytiga), which has was recently approved in the US, Canada and Europe for the treatment of patients with metastatic castration-resistant prostate cancer (mCRPC) who have received docetaxel chemotherapy. Another ongoing Zytiga company sponsored trials include: Phase III clinical trial in chemotherapy-nave mCRPC is ongoing and phase III studies in earlier indications are being developed; combination studies with docetaxel and other agents; and a randomized Phase II trial in breast cancer has just been initiated. Registration-directed Zytiga clinical trials form the treatment of prostate cancer are ongoing in Japan, China and other countries in Asia-Pacific. A pediatric program for the treatment of congenital adrenal hyperplasia associated with excessive androgen production has also been initiated. Other late stage programs at JNJ include Velcade, Siltuximab and Yondelis.

The Senior Programmer Analyst will be responsible for the development, quality control and documentation of statistical programs in support of department projects. He/She will assist in the planning and execution of programming activities for a single project and assist in the review and input into project requirements. The Senior Programmer Analyst will develop programs in support of clinical trial activities. Perform quality control in support of clinical trial activities. Maintain documentation as appropriate.

The Senior Programmer Analyst scope of responsibility includes: Deliver individual programming deliverables of medium to high complexity within a single project. Demonstrate full proficiency in technical/programming skills. The successful candidate will contribute broad knowledge of clinical trial activities.

Qualifications

The qualified candidate will have a minimum of a Bachelor's degree in computer science, mathematics or other related scientific discipline with 3 years experience programming and analyzing scientific data. Experience in a pharmaceutical and/or clinical trial environment is highly desired. Experience with FDA and ICH guidelines is preferred. Experience with SAS is highly desired. This position is located in Los Angeles, CA.

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