*Reply me on [email protected] <[email protected]>*

Greetings,



My name is Rugender and I am recruiter at eTeam Inc. eTeam Inc is a global
contingency staffing firm servicing fortune 1000 clients globally.We have
an excellent job opportunity with one of our client.



*Job Title: Sr. Trial Account Manager*

*Location: East Hanover,NJ *

*Duration: 6 Months*


* MOI: Phone Hire Onsite Role Client TCS*



*Job Description:*
Primary account manager for *Clinical Trials Portal (CTP), Interactive
Response Technology (IRT)* and ClinAdmin supporting the Clinical
Franchises, *Translational Medicines (TM), *Oncology and other businesses
as needed. Liaison between Development Informatics and members of the
business organization *(Country Pharma Organization (CPOs), Drug Supply
Management (DSM*), *Development Strategic Sourcing (DSS)* Statistics and
Data Management and *Clinical Quality Assurance (CQA)) *to ensure the
business needs of the end users (Clinical Trial Teams/Investigator sites,
etc.) are met. Consult Franchise/BU/TM/other Clinical Trial Teams on the
optimal value and use of various systems (*IRT, ClinAdmin, CTP, etc*.).
Responsible for 10-15 new plus 10-20 maintenance trials at any one time.
Ensures compliance with all required SOPs and business guidances.
IVRS
Proactively (using ClinAdmin data) evaluate planned trials as potential
candidates for IRT; assess risks, costs and benefits of utilizing IRT, use
of standard vs. customized modules
Responsible for the development, initiation, maintenance and *close-out of
IRT*
Responsible for completing Study Specification Worksheet/Decision Grid as
required
Review and prepare overview of costing proposal from vendors
Support the *CTT/DSM *in the selection of the preferred provider, user
requirement specifications (URS) and other relevant activities for IRT
initiation
Plan, perform and document user acceptance testing (UAT) of all systems
including report facilities with support of CTT prior to system going live
Ensure approval of related documents
Track usage of systems; assist in the development and implementation of
strategy to increase/improve usage of systems,

*Skills:*
Fluent English (oral and written), German desirable.
Minimum of a Bachelor s degree in a relevant field, such as a scientific or
health care discipline.
5+ years working experience and strong knowledge of the drug development
process.
Good knowledge of GCP, GMP and FDA part 11
Knowledge of clinical trial design and basic statistics
Familiarity with clinical trial systems
Thorough understanding of technology and tools
Excellent understanding of clinical development and clinical operation
processes.
Ability to work in a global team and matrix structure organization, meet
timelines and work with minimal supervision.
Great attention to accuracy and detail.
Strong team player
Excellent communication and presentation skills
Needs to be highly organized

Education:
BA/BS
-- 

*Regards*

*Rugen Nagar*


*e**Team Inc - "ACCCELERATED HIRES"*

Efficiency, Synergy, Expertise

1001 Durham Avenue, Suite 201, South Plainfield, NJ 07080

Desk: 732-248-1900 x489 (T) | Fax: 908-757-0800 (F)

Email: [email protected] || URL: www.eteaminc.com

*YIM/GTalk --> rugender.rgtalent*

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