If you are interested, please check the link:
http://ch.tbe.taleo.net/CH07/ats/careers/requisition.jsp?org=CUBIST&cws=1&rid=1026#!
Or send your CV to me.
________________________________
Scientist I, Clinical Pharmacokinetics
Location:
Lexington MA
Requisition Number:
1026
# of Openings:
1
________________________________
Description
Cubist is seeking a highly qualified individual for the position of Scientist
1, Pharmacokinetics. The primary function of a Scientist 1 is to work with the
Clinical Pharmacology project leader through all stages of a candidate drug's
development cycle. The candidate will be responsible for PK and PK/PD related
support such as study design, planning and execution, data evaluation,
analysis, and report preparation. Specifically, providing PK portions of
protocols synopses and protocols, dataset preparation and data merging for PK
analysis, non-compartmental and/or compartmental PK analyses, simple population
PK analysis, preparation of PK and PK/PD reports, publications, and
presentation of PK data in regulatory documents and meetings.
Key Responsibilities:
* Perform PK data evaluation, analysis, creation of tables, listings, and
figures, quality control check, and reporting
* Responsible for preparation of reports for studies with PK and PK/PD
aspects, CSR, and review and finalization of reports
* Assemble data sets for WinNonlin and NONMEM
* Independently perform non-compartmental analysis
* Responsible for preparation of PK, PK/PD components of internal
documents, briefing books, and regulatory submission documents (e.g. IND, NDA,
IB and other regulatory documents)
* Collaborate with Clinical Pharmacology project leaders and other
colleagues to generate abstracts and manuscripts for publication
Minimum Basic Qualifications:
* Master's (MS) with 5 plus years of relevant industry experience or Ph.D.
with 0-2 years of relevant industry (or post-doctoral) experience in
pharmacokinetics, pharmaceutical sciences, biological sciences, biostatistics,
or related field
* Strong analytical and programing skills
* Ability to evaluate and interpret standard pharmacokinetic and
pharmacodynamic scenarios and prepare PK reports
* A good working knowledge of Phoenix WinNonlin
* Familiarity with Microsoft Office, Excel, Power Point, and SigmaPlot
graphics
* Expertise with SPlus, basic SAS programming, and R
* Excellent writing and effective communication skills.
* Proven interpersonal, organizational and problem solving skills in a
matrix management environment
Preferred Qualifications and Experience:
* Experience with NONMEM, Phoenix NLME, Monte-Carlo simulation, and
clinical trial simulation preferred
* Prior experience and knowledge of PK/PD modeling and simulation, and
programming to assemble dataset desirable
Competencies:
* Demonstrates the ability to communicate clearly, concisely, and
effectively to express information in both written and oral context
* Aptitude to compile, analyze, and present data in a concise manner
* Proven capability to focus on delivering excellent results and
continually improve performance
* Demonstrated ability to set standards and hold self and others
accountable for performance and behavior in order to support high quality
Work Environment:
* Office
Physical Demands:
* None
Relocation Assistance is Available
To perform this job successfully, an individual must be able to perform each
essential duty satisfactorily within the context of the representative work
environment and physical demands described above. Likewise, qualifications
listed are representative of the knowledge, skills, and abilities required to
perform the position's essential functions. Reasonable accommodations may be
made to enable individuals with disabilities to perform the essential functions.
Cubist is an Equal Opportunity Employer (EOE). M/F/D/V
*LI-CP
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Avenue, Lexington, Massachusetts, 02421, U.S.A. 781-860-8660 www.cubist.com