Hi,


Please find the requirement below and answer ASAP with updated resume and
contact details to *ku...@osairtech.com* ...Thanks a lot...

------------------------------------------------------------

Resumes with the following information will be given preference.



Full Name:

Current Location:

Relocation:

Availability:

Work Authorization in US:

Contact Number:

Email:

Rate:



Please ensure all candidates have all skills listed under "Required Skills"
in their resume.

----------------------------------------------------------------



Title: Oracle Clinical Programmer
Contract Duration: 12 months
Environment: Corporate
Sponsorship Available: No
Location: Princeton, New Jersey
Minimum Requirements:
Qualifications

§         Bachelor's Degree in Bioinformatics, Computer Science or a related
field or equivalent experience

§         Minimum of five years experience creating data objects and
procedures in Oracle Clinical 4.5.x

§         Experience in a regulated environment, especially pharmaceutical
(21 CFR Part 11) and Phase I-IV studies

§         Strong interpersonal and communication skills; capable of
production technical support, training users and writing documentation

§         Team player who can multi-task, work effectively with members of
other teams, and communicate productively with clients

§         Good time management and organization skills; the ability to
prioritize own work to meet tight deadlines while maintaining the highest
standards of work


Description:
*Must be U.S. Citizen or Green Card Holder*

Responsibilities

§         Design, create, and validate new studies in Oracle Clinical; this
includes data object configuration, and validation documentation

§         Integrate protocol and charter requirements with internal business
practices to draft Data Quality Specifications

   - Review study documentation, translate study design parameters into
   Oracle Clinical data objects

§         Develop validation and derivation procedures that satisfy
constraints of study data quality plans

§         Manage validation and deployment of new studies

§         Plan and manage the update and re-validation of amended studies

§         Liaise with Data Management and Project Teams

§         Contribute, in regularly scheduled meetings, ideas and methods for
improving the design process

§         Document activities and work according to SOPs.  Write clearly and
accurately

§         Liaise with Data Managers of CLIENT’s various sponsors to discuss,
negotiate, and manage the electronic



*Regards,

Kumar Reddy,*

*Resource Specialist*

*
OSAIR Technologies LLC
301 N HARRISON STREET SUITE # 386
Princeton,NJ | 08540-3512
Voice : **201-546-3813*

*Fax :732-289-6076
ku...@osairtech.com*

*www.osairtech.com*

*"We want to be your Trusted, Preferred & long Term Partner"*

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