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Job Title: Data Management, Sr. Associate I
Description:
The candidate will be responsible for assigned study data management activities including, but not limited to, coordination of CRF design, development, review and sign off activities; provide CRF completion guideline, CRF training and Data Review Guideline to staff and vendors; coordinate database live and close out activities, manage query flow and implement quality control plan. Develop and maintain timelines and coordinate study database lock activities. The individual will participate in reviewing vendor audit plan, as needed, and statistical analysis plan; manage vendor and partner relationship, including participation in vendor qualification and selection, and monitor vendor performance.
Qualifications:
Candidate must possess a BS in biological sciences or other medically related areas; knowledge in oncology clinical trials a plus. A minimum 3 years of clinical data management experience in the biotechnology/pharmaceutical industry. The candidate must have the ability to work on routine assignments with minimal supervision. The individual must have working knowledge of GCP, excellent organizational skills and ability to prioritize assigned tasks. He/she must be able to work under tight timelines, possess excellent communication skills, demonstrate good negotiation skills, and take initiatives. Familiarity with data management software (e.g., PageMaker, Oracle Clinical) is a must.
Compensation:
Commensurate with experience
Date Posted: 04/07/2008
Email Résumé to info@cougarbiotechnology.com

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Cougar Biotechnology, Inc.
10990 Wilshire Blvd, Suite 1200
Los Angeles, CA 90024
(310) 943-8040 Main
(310) 943-8059 Fax |