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Join a very successful CRO in Los Angeles and provide your technical expertise and programming support for complex clinical trial projects. You will participate on projects as a team player, have an opportunity to really utilize your knowledge, and interact with clients (both internal and external. You will help devise creative solutions and enhance the decision making process.
You will be responsible for coordination, planning, development, and analysis for SPS tasks which includes analysis file creation, dictionary coding, statistical tables, appendix listings and patient profiles. You will perform necessary departmental quality control procedures and documentation. Serve as technical analyst for programming activities related to complex projects such as NDA or Treatment IND projects, especially during planning stages.
Please send me a copy of your resume attached as a Word document.
Susan Bernstein
Tristaff Group
858-453-1331
4350 Executive Drive
La Jolla, CA 92121
susan[at]tristaff.com
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Biostatistician
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Nobody
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posted on
Saturday, November 29, 2003
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Biostatistician
This client is seeking a highly-qualified Biostatistician to support all aspects of clinical investigation, including design and analysis of clinical studies, collaborate with investigators affiliated with a major medical school, grant and protocol development and review, and teaching and mentoring of junior investigators.
The individual must have:
*an M.S. or Ph.D. in statistics or Biostatistics
*a strong record of collaborative research
*3+ years experience
*excellent interpersonal skills
*excellent oral and written communication
*multitasking capability to handle numerous simultaneous projects
*a strong commitment to excellence in research.
Candidates with broad consulting interests who enjoy collaborating with physicians and research staff are encouraged to apply. Expertise in study design, grant writing, clinical trials, case-control and cohort studies, statistical genetics, hierarchical, longitudinal, survival, nonlinear, SAS.
The Biostatistician will have a research associate appointment. and not a clinical trials coordinating center.
Interested candidates should send a letter of interest, CV, writing sample, and reference information to resumes@workwondersstaffing.net
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