*Note: Please forward resumes to mah...@trustek.com <mah...@trustek.com>*

Position   :  Oracle Clinical Consultant
Location  :  Berkeley heights, NJ
Duration  :  12 Months

*SURE SHOT CLOSEABLE POSITION.*

Responsibilities will include, but are not limited to:
Develop, program, test and maintain clinical trial databases and data entry
screens using Oracle Clinical or Central Designer in accordance with
Celgene standards
Review computer validation/edit checks for in-house and outsourced studies
Develop, program, test and maintain computer validation/edit checks in
PL-SQL and/or SAS
Develop, program, test and maintain data review listings in Oracle
Clinical, Inform, Jreview and/or SAS for data review purposes
Perform external data loads, i.e., labs, ECGs, etc., as needed. Act as
liaison with vendors to establish transfer specifications and Celgene
standards
Validate peer programming
Participate in and lead team meetings when appropriate
Act as primary CRO contact, when necessary, to ensure that Celgene
standards are implemented in all studies
Provide technical expertise and support to Data Management team
Control access to database and perform snapshots, database lock and freeze
activities
Make data, including interim data, available to company personnel and
regulatory agencies when required
Perform post processing of data extracts in accordance with Celgene
standards to be delivered to Biostatistics
Routinely interface with cross-functional team members
Influences other functions and represents as DBO technical expertise
Internal team leader who decides best course of action
Coach and advise junior programmers to identify problems and solutions 1.
Manage outside CROs and consultants:
Review clinical programming activities and costs in contracts
Assess CRO data management systems for regulatory compliance
Interact with CROs in the design and development of databases that are
compatible with company needs
Monitor progress of clinical programming activities in CROs
Participate in regular team meetings and provide input when appropriate

2. Other Activities
Participate in the development of clinical programming SOPs and the
development/optimization of clinical programming processes from study start
up to database lock.
Routine interface with cross-functional team members in creating an
appropriate database, data quality assurance, and support of data cleaning
activities
Direct responsibility for supervising and training junior clinical
programmers in the performance of their duties

Managing project priorities and timelines Skills/Knowledge Required:
BS/BA degree or equivalent in a relevant scientific discipline with a
minimum of five years experience
Advanced knowledge of clinical database design is a must (Inform, Oracle
Clinical or other systems).
Experience managing clinical programmers
Participation in at least one NDA is preferred
Good communication skills; ability to work in a team environment with data
managers, medical personnel, clinical monitors, statisticians, programmers,
and medical writers
Knowledge of FDA/ICH guidelines and industry standard practices regarding
programming
Medical or mathematics/computer science background a plus
Detailed knowledge and experience in case report form design, central
laboratories, programming databases, query resolution, data validation
Knowledge of SQL and SAS programming
Computer

Skills:
detailed knowledge of clinical database design (Oracle Clinical or Inform),
proficiency with SAS data sets and conversion procedures, knowledge of MS
Office program suite
Knowledge of clinical trial design and basic statistics (a plus)

*Thanks & Regards: *

*Mahesh, *

*Sr. Technical Recruiter *

*Trustek Inc *

*Office: 732-393-1313 ext-112| *

*Fax: 001(866) -294-1314 |*

*E: mah...@trustek.com <mah...@trustek.com> | www.trustek.com
<http://www.trustek.com> |*

*1001 Durham Ave,Suite 306 | South Plainfield, NJ 07080 |*



*Yahoo IM: mahesh.saxon *

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