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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