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Oracle Clinical Programme - C2H

Title: Oracle Clinical Programmer

Type: 6 months contract to hire

Required Skills Oracle Clinical 4.5.x, RDC, PL/SQL, Data Objects

Reports to: Manager, Oracle Clinical Data Base and Application Development

VISA: THIS JOB REQUIRED US CITIZENSHIP, GREEN CARD, EAD OR TN1 VISA. NO H1b candidates will be considered

Overview:

This person will design and create Oracle Clinical studies in conjunction with the clinical data coordinators, d study project team leaders. This includes leveraging pre-existing GLib data objects, creation of new objects and creation of validation documents

Client is a leading CRO specializing in Oncology clinical studies for various pharmaceutical companies. They have medical imaging radiology applications with Oracle Clinical, Siebel Clinical, Workflow software running in Microsoft .NET platforms.

The individual will work w/ Database group and clinical technology group from Protocol Design to Project Completion.

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 transfer of clinical data from the sponsor to Client.

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)
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

Oracle Clinical Programmer

Title: Oracle Clinical Programmer

Tupe: Contract - 12 months

Required Skills Oracle Clinical 4.5.x, RDC, PL/SQL, Data Objects

Reports to: Manager, Oracle Clinical Data Base and Application Development

VISA: THIS JOB REQUIRED US CITIZENSHIP, GREEN CARD, EAD OR TN1 VISA. NO H1b candidates cannot be considered.

Overview: This person will design and create Oracle Clinical studies in conjunction with the clinical data coordinators, and study project team leaders. This includes leveraging pre-existing GLib data objects, creation of new objects and creation of validation documents

The individual will work w/ Database group and clinical technology group from Protocol Design to Project Completion.

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 transfer of clinical data from the sponsor to Client.

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)
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

Computer Systems Validation Engineer

6 - 12 Months

Princeton, NJ

Skills: Writing/Implementing Validation Deliverables, Independently formulate validation projects for small projects, Software Testing (Off the shelf and home-grown software) of database products, and Oracle

Work Authorization - US Citizen, Green Card, EAD, TN1 (client cannot consider H1b visa candidates for this role)

Summary:

Client is a fastest growing Oncology Clinical studies research organization that uses Oracle clinical, Siebel, Unix/Linux/Widows based Imaging, Workflow, Submissions, Clinical Trials, and Data Management systems - off the shell and customized components.

This person will perform validation of computer systems in an FD Aregulated environment. Responsible for preparation of change control and validation documents, preparation of summary reports, and preparation of test scripts

Responsibilities

· Preparation of change control documents, including validation approach

· Prepare all validation documentation including Validation Plans, OQ Protocol and other

· required documents

· Development of test strategies for Off-The-Shelf and custom applications

· Preparation of OQ/System and UAT test scripts

· Coordination of testing, including evaluation of test results; oversees and reviews

· validation area processes and procedures.

· Compilation and quality review of validation binders

· Preparation of validation summary reports

· Document activities and work according to SOPs. Writes clearly and accurately

· Coordinate all validation activities by constant communication with affected departments

· and personnel;

Qualifications

· Minimum of 3 to 5 years computer system validation experience in Pharmaceutical

industry; three years desirable.

· BS Degree with experience in validation and software development lifecycles, GCPs, 21

CFR Part 11.

· Excellent written and verbal communication skills.

· Experience in a regulated environment, especially pharmaceutical (21 CFR Part 11),

· Good time management and organization skills; the ability to prioritize own work to meet

tight deadlines while maintaining the highest standards of work

NOTE: THE JOB REQUIRES UNRESTRICTED VISA AUTHORIZATION SUCH AS

US CITIZENSHIP, US GREEN CARD, EAD AND/OR TN1

NO H1 CANDIDATES WILL BE CONSIDERED.

Oracle Business Intelligence Developer

Keyskills: Oracle Business Intelligence, PL/SQL

Overview:

Our client is a multinational conglomerate with offices across the globe with emphasis on Information Technology services.

Description:

The client has various divisions across the USA running different businesses. They use ERP/CRM/SCM applications software supporting various business units.

They want to design and develop a Management Level system using Oracle Business Intelligence softare suite.

This application will allow various corporate heads to access all the relevant data from various sources/buiness units.

The individual will design/develop/roll-out prototype and final version of the application.

Requirements:

Bachelor's degree in Computer Science or relevant field.

10+ years of IT experience.

3-5 years of Business Intelligence experience especially with architecure, design, development and implementation.

Proven experience in SDLC

Track record in working w/ business/funcational users

Exceptional communications - presentation, verbal, written skills.

LOCAL CANDIDATES PREFERRED

ALL CANDIDATES MUST BE AVAILABLE FOR ON-SITE INTERVIEWS AT THEIR OWN EXPENSES.

CANDIDATES MUST HAVE UNRESTRICTED WORK AUTHORIZATION FOR ANY EMPLOYER - NO VISA SPONSORSHIP.

Oracle APEX Developer

Keywords: Oracle APEX (Application Express) - formerly knows as HTML DB

Job Summary:
Client has developed an Inventory Management System using Oracle 10g/Forms/Reports w/ Oracle ADF. They're in the process of allowing its users to have access to reports online using Oracle APEX (Application Express).

Use APEX tools such as Applicaiton Builder, SQL Workbench and Utilities to develop/manage applications.

Use the tools to pull the data from Forms and write web based reports, charts, etc.

The client is developing next generation Inventory Management System that will use Presentation Layer using Forms, Business Logic/middle layer using Packages and Backend layer using PL/SQL.

Requirements: The position requires a Bachelor degree in any field and 3 - 5 years of progressive experience in software applications analysis, development and design, of which at least 3 years must be specific to the Form 6i design/development.

Experience with Oracle APEX (and./or HTML DB) Development experience is required.

The client uses Forms based on Complex Views and not on tables
The Candidate must have developed at least one compelx APEX application in the past one year.

Must possess excellent communications skills.

LOCAL CANDIDATES PREFERRED.

CANDIDATES MUST BE AVAILABLE FOR ON-SITE INTERVIEWS AT THEIR OWN EXPENSES.

CANDIDATES MUST HAVE UNRESTRICTED WORK AUTHORIZATION FOR ANY EMPLOYER W/ VISA TRANSFER/SPONSORSHIP.

Oracle Forms/Report Developer

Keywords: Oracle Forms 6i/10g, Reports 6i/10g, PL/SQL

Job Summary:

Develop, modify, test, maintain and document database applications for clients requiring customization of highly complex sales, purchasing, order entry and inventory control systems software and develop new custom interfaces predominantly in an Oracle relational database environment.

Develop multi-level screens/forms for complex transactional applications.

Maintain, support and enhance Forms 6i and develop new application using Forms 9i/Oacle 10g

The client is developing next generation Inventory Management System that will use Presentation Layer using Forms, Business Logic/middle layer using Packages and Backend layer using PL/SQL.

Requirements: The position requires a Bachelor degree in any field and 3 - 5 years of progressive experience in software applications analysis, development and design, of which at least 3 years must be specific to the Form 6i design/development.

Experience with Oracle Forms Development experience is required.

The client uses Forms based on Complex Views and not on tables

Must know how to do data manipulation on packages

Use Navigational methodologies using Tab Canvasses

The candidates must have developed Presentation layer using Forms (but not using internal of Forms) and Data Access/middle layer using QP/CP Packages and Procedures

The environment is very intense and high paced with weekly deliverables.

Must possess exellent communications skills.

LOCAL CANDIDATES PREFERRED.

CANDIDATES MUST BE AVAILABLE FOR ON-SITE INTERVIEWS AT THEIR OWN EXPENSES.

CANDIDATES MUST HAVE UNRESTRICTED WORK AUTHORIZATION FOR ANY EMPLOYER W/ VISA TRANSFER/SPONSORSHIP.

Oracle Clinical Study Designer

ORACLE CLINICAL STUDY DESIGNER

DURATION: ONE YEAR CONTRACT TO

HIRE

LOCATION: PRINCETON,

CLIENT: CLINICAL RESEARCH ORGANIZATION (CRO)

Overview:

The client is a leader in Oncology clinical studies in the country supporting medical imaging and radiology aspects all Oncology clinical studies for majority of the Pharmaceutical companies w/ global support. The client has been growing consistently for the past 5 years w/ 20% growth year over year.

Position Overview

This person will design and create Oracle Clinical studies in conjunction

with the Oracle Clinical developers, clinical data coordinators, and study

Project team leaders. This includes leveraging pre-existing GLib data

objects, creation of new objects, creation of validation documents, and

delineation of procedure requirements.

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

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

mentor junior colleagues.

Participate in knowledge transfer
Liaise with Data Managers of Client’s various sponsors to discuss, negotiate, and

manage the electronic transfer of clinical data from the sponsor to Client.

Qualifications

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

Experience

Minimum of one year expert-level experience with Oracle Clinical, with the most recent being with Oracle Clinical/RDC 4.5.
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

Note: No third-party sub-contracting H1b employees. All candidates must have unrestricted Work Authorization – US Citizenship, Green Card, EAD, TN1

Oracle PL/SQL Developer

Title: ORACLE PL/SQL Developer

Reports to: Manager, Application Development
Duration: 12 months contract

Location: Princeton, NJ

Client is looking for a seasoned Oracle, PL/SQL Developer who can develop, maintain, and update database objects, stored procedures, triggers, and functions for an Oracle Clinical application supporting various clinical studies. Client works with various pharmaceutical companies with their clinical studies. Each clinical study is mapped and managed by Oracle Clinical Data Management application.

As an Oracle Developer, your application data resides in the Oracle Clinical application. You’ll develop various procedures/function that complies with the FDA compliant Standard Operating Procedures.

Responsibilities:

Develop data base objects using PL/SQL to support the study specific requirements in Oracle Clinical
Perform effective code reviews, maintaining standards and good practices
Assist in troubleshooting operational issues, resolve while maintaining good compliance practices.
Document activities and work according to SOPs.
Work with development team and users to enhance study development process
Participate in creation, maintenance and update of development standards and best practices.
Translates business requirements into functional application requirements and

logical data model requirements

Position Required Skills:

· BS degree in computer science or related, technical field

· Minimum 5-7 years of development experience.

· Expert level development skills in

o PL/SQL, SQL,

o UNIX Shell scripting, and

o UNIX commands

· Ability to thrive in a team-oriented organization

· Experienced in a regulated environment, especially pharmaceutical

· Proven experience in the full systems life cycle

· Excellent time management and organization skills; the ability to prioritize work to meet tight dead lines while maintaining the highest standards of quality.

· Strong interpersonal and communication skills; capable of production technical support. Training users and generating documentation.

· Oracle Clinical experience is a plus.

NOTE: WE CAN’T CONSIDER ANY CANDIDATES W/ H1B VISAS AND ALL CANDIDATES MUST HAVE UNRESTRICTED WORK AUTHORIZATION. LOCAL CANDIDATES ONLY.

When you apply online, plese enter your contact number and email id for us to respond to your resume. Thanks

Senior Medical Imaging Engineer

Overview:

Leads the development and integration of CLIENT’s medical imaging systems and applications.

The Senior Medical Imaging Engineer works with the IS Director and IS Project Managers in order to analyze current processes to deliver internally developed systems and the introduction and integration of

Commercial products to improve CLIENT’s imaging reliability, efficiency and scalability. The

Senior Medical Imaging Engineer also provides mentoring, leadership and training to other Imaging

Engineers within IS.

As a Senior Medical Imaging Engineer, you report to the Director and play a very crucial role in successful design/developmen, integration/implementation of medical imaging systems.

CLIENT: Client is a fastest growing medical imaging research organization with an annual growth of 25% or more for the past 4 years. The company uses the medical platforms/tools/systems to provide services to oncology studies for Fortune 500 Pharmaceutical companies around the world. They use both C#/Windows and C++/Java/Unix development.

Responsibilities

· Gathers requirements, builds designs, codes, documents and maintains software according to CLIENT’s standard software lifecycle methodology and SOPs.
· Provides programming and algorithm development and produces technical design documentation suitable for use in developing verification and validation test plans, protocols, and requirement traces.
· Delivers applications that produce, edit and analyze DICOM header and image data
· Evaluates imaging technologies vendors and systems for use within CLIENT
· Drives the integration of new tools and systems within CLIENT’s imaging workflow
· Assists in the out-sourcing and support of externally developed and off-the-shelf applications
· Provides support and advice to the Clinical Operations and Information Technology Departments with respect to digital imaging applications
· Performs third level software support as needed

Qualifications

· MS/Ph.D. in Electrical Engineering, Computer Engineering, Physics, Bioengineering or Life Sciences and at least 3 years of relevant experience using various imaging platforms
· Minimum of 6 years recent contiguous experience with C/C++/C# or Java in Windows or Unix environments
· Demonstrated significant volume of imaging code used in tumor tracking or oncology related clinical trial work
· Strong programming and analytical skills
· Experience with medical imaging devices and software (especially CT, MRI & PET) using DICOM
· Demonstrated knowledge in developing imaging analysis and viewing applications
· Must be able to work proficiently in a small team environment, and have a strong sense of team and project
· commitment
· Must have excellent communication skills and enjoy working in an interdisciplinary environment
· Experience in following established software design control procedures
· Experience developing code for medical devices, or similar regulated industry is highly desired
· Experience in a regulated environment, preferably pharmaceutical or medical devices
· Experience with 21CFR Part 11 validation and HIPAA

Note: The client cannot consider any H1 sponsorship/transfer candidates and will consider only those who has unrestricted work authorization such as, US Citizenship, Green Card, EAD, TN-1.

The client will consider a Contract to Hire or a Direct Hire (Permanent) candidates.

Oracle Clinical CRF Designer

Duration: 6 months contract to Hire/Perm

Location: Princeton, NJ

Skills: Oracle Clinical RDC 4.5, CRF design/annotation/review,User Interface design principles, GLib

Overview: This person will design and create Oracle Clinical studies in conjunction with the Oracle Clinical developers, clinical data coordinators, and study project team leaders. This includes leveraging pre-existing GLib data objects, creation of new objects, creation of validation documents, and delineation of procedure requirements.

Responsibilities

Design, create, and validate new studies in Oracle Clinical; this includes data object configuration, Glib maintenance, CRF design, and validation documentation
Integrate protocol and charter requirements with internal business practices to draft Study Data Quality Plans
Manage validation and deployment of new studies
Plan and manage the update and re-validation of amended studies
Delineate requirements and scheduling of data listings and patient data reports
Liaise with Data Management, Clinical Operations, submission team, business development, and medical affairs groups
Document activities and work according to SOPs. Write clearly and accurately
Mentor junior colleagues, engender knowledge transfer

Qualifications

Bachelor's Degree in Life Sciences, Pharmacy or Nursing or equivalent experience
Formal or on-the-job training in clinical trial methodology and Good Clinical Practice (GCP)
Minimum of three years expert-level experience with Oracle Clinical, with the most recent being with Oracle Clinical/RDC 4.5.x
Extensive CRF design experience, firm understanding of user interface design principles
Team player who can multi-task, work effectively with members of other teams, and communicate productively with clients
Experience in a regulated environment, especially pharmaceutical (21 CFR Part 11),
Good time management and organization skills; the ability to prioritize own work to meet tight deadlines while maintaining the highest standards of work

Note: Candiates must be available for in-person interview and must have unrestricted work authorization to work for any employer without any transfer/sponsorship of visas.

Oracle Clinical Programmer

Duration: 6 months contract to Hire

Location: Princeton, NJ

Must have Skills: Oracle Clinical 4.5, RDC, PL/SQL

Overview: This person will perform Oracle Clinical programming activities in conjunction with the Oracle Clinical Study Designer and other OC developers, and will manage/maintain the Oracle Clinical database. The role designs and develops study data objects, validation/derivation procedures, and data extract views; maintains reference codelists, and prepares datasets for delivery to clients.

Responsibilities

Develop validation procedures that satisfy constraints of study data quality plans
Create derivation procedures that meet reporting requirements and enhance data entry operations
Maintain/manage data extract views and create data extracts, as needed
Review study documentation, translate study design parameters into Oracle Clinical data objects
Maintain, verify, and improve OC database backup and recovery procedures
Monitor OC database parameters, adjust configuration on an as-needed basis
Provide patch/release analysis and guidance, apply and validate relevant updates
Document activities and work according to SOPs. Writes clearly and accurately
Manage the development, support, and administration of multiple IS systems
Maintain a safe work environment. Reports workplace hazards immediately

Qualifications

Minimum of BS degree in Computer Science or related field or related experience.
Minimum of three years experience creating data objects and procedures in Oracle Clinical 4.5.x
Experience using a clinical data reporting tool, such as Integrated Review
Expert PL/SQL skills using.
Demonstrated experience developing/managing Oracle databases in Oracle Clinical environments
Effective communication skills; a cooperative and team oriented approach
Experience in a regulated environment, especially pharmaceutical (21 CFR Part 11),
Good time management and organization skills; the ability to prioritize own work to meet tight deadlines while maintaining the highest standards of work

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

Senior Software Engineer - 0901

Senior Software Engineer

Permanent/Full-time

Must have Skillset: C++/Linux/Unix, MySQL/SQL Database, IPC, Multi-threaded/socket programmign for C++/Linux/Unix apps

IMAGINE WORKING ON SOFTWARE PRODUCT SOLUTIONS THAT SOLVE THE FASTEST GROWING DATA STORAGE PROBLEMS FACED BY HEALTHCARE AND OTHER INDUSTRIES.

YOU’LL BE WORKING ON DEVELOPING SOFTWARE SOLUTIONS THAT HANDLE 1000 TIMES OF TERABYTES ACORSS THE TNERTPRISE.

READ MORE ---
Client is a leading privately held (and profitable) service provider of digital image storage and archiving solutions for the HEALTHCARE community. Their software solutions handle large volume of data. They have clients in the US and Canada.

The client is developing database intensive archival/retrieval product solutions for healthcare industries. Now, they are planning to add additional features that will handle mega storage as well as enterprise wide document sharing of all formats. The next generation of the software products will handle not only images but all formats of data across the enterprise. C++ is used w/ Linux/MySQL for the development.

The person we are seeking will be a Senior Software Engineer to work core product, which is written in C++ and Java and deployed on a Linux (SuSE) platform. The Senior Software Engineer will help create new features/products and will also help support the company’s current software products. This position requires experience and knowledge in how to design and implement highly robust and scalable solutions. The ideal candidate has strong low-level internals (networking, sockets, file system / i-nodes, memory management, multi-threading) skills.

The Senior Software Engineer conducts all software development life-cycle activities including requirements gathering, design, code, etc. for the Software Development Group. The specific responsibilities of this position include:

· Design, develop, and implement software according to guidelines.

· Debug and maintain software.

· Help track problems in the field.

· Work with Q/A with each release.

· Develop test/debugging tools to help Q/A and Support.

· Assist Technical Services (responsible for day-to-day operations on the Data Center) with deployment and usage issues.

· Document software.

· Develop and maintain expertise in one or more of the following healthcare IT standards:

· DICOM, IHE, HL7, XDS, CCA, etc. As standards expert for company, keeping abreast of all standards related trends; standards liaison to and internal business units, customers and partners.

Preferred candidates will possess more 5 – 7 years of relevant experience in designing and implementing major database driven systems.
Serious candidates must have proven C/C++ and Linux experience as well as hands-on experience with any major DBMS. MySQL is a definite plus.
DICOM and HL7 are currently used and will add XDS (cross Enterprise Document Sharing) Standards experience a big plus.
Strong communication skills are a must.

Position is located in Stamford, CT. Compensation package will include a base salary, revenue sharing and an attractive stock option plan
Strong communication skills are a must.

Compensation includes a good base + GUARANTEED BONUS + STOCK OPTIONS AND MORE

NOTE: This is NOT a suitable job for those candidates who’ve worked only on IT projects instead of SW Engineering product development

NO RELOCATION AVAILABLE FOR THIS ROLE

NO THIRD PARTY CANDIDATES

Keywords: C/C++, Java, MySQL, UNIX/LINUX, XDS, HL7, DICOM, Storage, Archiving, Retrieval, Rules-based application.

Oracle Apps Developer

Job Title: Oracle PL/SQL Developer
Location: Cleveland, OH
Duration: 6 months
Keywords: Oracle, PL/SQL, Forms 6i, Order Management, Shipping, Customization

Client is a $B medical devices firm with implementations of Oracle Apps (OM, OE, Financials), SAP, Siebel, PLM and other applications. This job is within the Oracle Apps group with Order Management emphasis.

Client is planning to implement changes in their existing Oracle Applications, to make calls to a freight calculator application (example Flagship from Kewill), to calculate freight charges and apply to the order and customer invoice. They are looking for a technical resource with good knowledge of OM, iStore, Advanced Pricing and Shipping. Advanced Pricing experience should include setting up custom pricing attributes, qualifiers and modifiers. A good understanding of the complete life cycle of an order is required.

Candidate should possess strong technical skills in Oracle development tools including SQL, PL/SQL, Workflow and Form 6i customization. SQL tuning knowledge and experience is a must. Freigh Calculators products such as, Flagship from Kewill Flagship (Enterprise Shipping Management solutions) is a sure WINNER.

Knowledge of and experience in freight calculators like Flagship will be a plus.

BS degree with 5 - 10 years of Oracle, PL/SQL, SQL tuning, Forms 6i and at least 2 projects w/ Oracle Apps.
6 months project experience with Freight Calculators is a big plus.

NO RELOCATION