Fwd: פרסום משרת סטטיסטיקה חדשה בחברת טבע
Tal Galili
From: Maya Blank <Maya....@teva.co.il>
Date: Sun, Oct 7, 2018, 13:53
Subject: פרסום משרת סטטיסטיקה חדשה בחברת טבע
To: tal.g...@gmail.com <tal.g...@gmail.com>
היי טל,
נעים מאוד, שמי מאיה ואני חלק ממערך הגיוס של חברת טבע.
נפתחה לנו משרה חדשה ובכירה בתחום הנ"ל.
אודה לסיוע ופרסום המשרה אצלכם :
Associate Director Statistics
The Associate Director, Statistics position is for a skilled statistician, with experience in clinical development, especially in early stage clinical development and pharmacokinetics. The applicant is expected to provide statistical leadership and strategy for a program and studies. The applicant must be a strong individual contributor, demonstrating creative and strategic thinking and knowledge of modern trial design. This position will be located in Netanya, IL.
- Strategic and scientific leadership to the design of the early clinical studies as part of comprehensive clinical development, including statistical leadership in clinical pharmacology and bioequivalence.
- Effective partnership with R&D functions including clinical Pharmacology, Pharmacometrics, clinical and regulatory to drive quantitative decision and enable successful programs
- Solid knowledge of statistical principles, methodology and software is required.
- Ability to use of innovative trial designs
- Knowledge and understanding of the clinical pharmacology model of the drug and of the therapeutic area
- Authors statistical section of protocols and statistical analysis plans or oversee their preparations
- Provides statistical input for CRF design
- Conducts, or oversees the conduct of, analyses to support study reports and publications
- Involved in CRO selection for outsourced activities, and oversees the CRO work
- Consults and mentors other statisticians on methodology and trial design
Qualifications:
- MA/MS/PhD in Statistics/Biostatistics (or related field) with a minimum of 10 years of related experience
- Excellent oral and written communications skills
- Expert in planning, analysis and reporting of clinical trials
- Ability to work in a global organization and in an outsourcing model
- Good organizational and problem-solving skills
- Demonstrated technical qualities
- Creative and strategic thinking
- Ability to program using SAS, knowledge of R is beneficial
- Knowledge of CDISC SDTM and ADaM
- Experience with regulatory interactions in the US and outside
- Demonstrated ability to deliver quality products with efficiency
תודה,
|
Maya Blank
Cell: +972 (3) 9166829 |
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