Law

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Please send resumes to praveen@addonusa.com

BI Architect  

Location: NY

Duration: 6+  months CTH

 

A person with strong professional consulting skills, Financial Domain Experience and the ability to communicate well with Management & user community. Must have min of 10-12 yrs of relevant exp. He/She should be able to perform below tasks.

·         Analyzing user information needs and accessibility requirements for front-end BI applications

·         Designing functional specifications for BI front-end applications

·         Understand various subject area & define end to end BI solution (Market product, Profitability, Credit Risk etc.)

·         Define the Information delivery strategy

·         Design and implement a scalable OLAP cubes and reporting framework

·         Define Standards for Semantic Layer and Reporting modules

·         Design Information access layer and Portal Integration Strategy

·         Create dashboard design patterns, standards, and templates

·         Design and implement BI metadata and data dictionary design and standards

·         Recommend Data Access/BI Tools to Business

·         Devise the BI Content Testing & Migration Strategy

·         Design the Information access and BI Security Strategy

·         Supporting Organization in integration efforts to merge BI platforms with enterprise systems and applications

·         Strategy to support EUDs

·         Recommendations for  Performance tuning and query optimization

·         Recommend BI Self-Service Tool/Strategy

·         Recommend BI Center of excellence strategy

 

 

BO&OBIEE Lead/Analyst

Location: NY

Duration: 6+  months

 

 

A person with Financial Domain Experience and good communication skills. Must have min of 8-10yrs yrs of exp working with BO R4 & OBIEE . He/She should be able to perform below tasks.

·         Analyze current reporting platform

·         Evaluate Business needs from BI and Identify current gaps

·         Define/Design BI/OLAP/MOLAP Strategy

·         Design BO Universe/OBIEE Physical layer etc.

·         Design BO reports, dashboard, KPIs etc.

·         Re-platform legacy BO reports to new CDW data mart

·         Provide inputs for Portal Integration and Report Distribution

Design Macros & leverage BO SDK

 

 

DW BI Architect 

Location: NY

Duration: 6+  months CTH

 

Person must have strong professional consulting skills, Financial Domain Experience and the ability to communicate well with Management & user community. Must have min of 10-12 yrs of exp with expertise in below areas.

·         Assess requirements, Direct the discovery process and establish the BI strategy

·         Define the overall data warehouse architecture (e.g., ETL process, ODS, EDW, Data Marts)

·         Define data strategy – Data management, Data integration & DQ strategy

·         Define technical requirements, technical and data architectures for the data warehouse 

·         Devise the implementation plan and Infrastructure Strategy

·         Model the Physical data base design, including Star schema and data mart design, Snowflake schema design

·         Evaluate the Change data design, including slowly changing dimensions and Operational data store design.

·         Design data migration, archival & Retention Strategy

·         Evaluate DWH Data/Tools for best fit

·         Design and direct the ETL process, including data quality and testing

·         Support reference data architecture & MDM strategy for EDW

·         Design and direct the information access and delivery effort for the data warehouse 

·         Define and direct the implementation of security requirements for the data warehouse

·         Define meta data standards, capture and management strategy

·         Devise the DW operations management including Process architecture and System processes

·         Define production release requirements and sustainment architecture

·         Define Real time / Near real time data strategy for future DWH – Via IBM Web service, ESB – SOA

 

 

 

Business Analyst with Big 4 Consulting background

Location: Anaheim, CA

Duration: 9-12 months +

 

 

ALL candidates must have excellent communication skills.  Also, the hiring manager is interested in candidate with Big 4 Consulting background: Deloitte, KPMG, Accenture, Kaiser Permante.  If you find a candidate with experience with one of those companies, Client is interested in speaking with him TODAY!

 

Requirements:

 

·     Bachelor?s Degree or higher in Computer Science, Engineering, or related field

·     8+ years advanced IT experience in large enterprise environments in a consulting role

·     7+ years in experience writing business or functional requirements.

·      7+ years in experience analyzing data, policies and requirements to understand current state and prepare future state

·     Experience documenting requirements for dashboards, scorecards, and KPIs

·     Knowledge or experience with frameworks, notations & concepts, Agile, MDM BPMN, SOA, data normalization & denormalization

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Please do let me know if any one fits for this position

Thanks & Regards

Praveen Kumar

Technical Recruiter | Addon Technologies | Website: www.addonusa.com

phone: 734-956-4737 ext-168 | Fax: 734-418-2603 | email: praveen@addonusa.com|

N . Laurel Park Drive, Suite #513, Livonia, MI-48152.

The Lord is my rock, and my fortress, and my deliverer; my God, my strength, in whom will trust. Psalm 18:2

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Hello,

 

I have an urgent position with client in Alpharetta, GA. Please let me know your interest for the same.

 

Business Analyst with strong ITSM Experience

Job Location: Alpharetta, GA
Duration: 9 months contract

 

Description

• This will be the new implementation of ITSM
• Experience implementing a Service Management Tool Suite 
• Strong technical skills 
• Experience providing program or cross-project coordination 
• Assume overall accountability for a group of projects upgrading the ITSM Tool Suite 
• Responsible for the creation, development and active management of the overall upgrade & decommissioning schedule 
• Responsible for actively managing dependencies, issues, changes and risks across the related group of projects 
• Responsible for providing the overall status of the tool suite upgrade 
• Nice to have PMP and ITIL Foundations certifications.

 

 

Thanks and Regards,

 

Pramod Kumar | Dominion Technology Service Corp |D: 804-859-7030| F: 804-237-0486|

3900 Westerre Parkway, Suite 300, Richmond, VA 23233

E-Mail: pkumar@dtscinc.com | Gtalk: pramodkumar79 | Yahoo: pramodkumar79 |Joining Our VMS

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Hello,

 

I have an urgent position with client in Newport Beach, CA. Please let me know your interest for the same.

 

MS Access Database Developer/Analyst

Location: Newport Beach, CA

Duration: 6 Months+

 

• Expertise in MS Access 2010 development and support
• Strong VBA & SQL development skills
• Advanced database design & architecture experience
• Detail oriented is a must
• This person will do compensation for a large corporation so will come across some large comp numbers up to a $1 mil+ in a few cases
• Would be nice if they had HR Compensation exp but not a requirement
• Someone who has a business analyst background is perfect
• Professional work environment 

 

 

 

Thanks and Regards,

 

Pramod Kumar | Dominion Technology Service Corp |D: 804-859-7030| F: 804-237-0486|

3900 Westerre Parkway, Suite 300, Richmond, VA 23233

E-Mail: pkumar@dtscinc.com | Gtalk: pramodkumar79 | Yahoo: pramodkumar79 |Joining Our VMS

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How obsessed are we, you ask?  Well, when (courtesy of Mealey's; we probably wouldn't have seen the case at all otherwise) we read McCormack v. Hiedeman, ___ F.3d ___, 2012 WL 3932735 (9th Cir. Sept. 11, 2012), we didn't think about pro-life. pro-choice, or even preliminary injunctions.


No, we thought about FDCA preemption.

You see, going all the way back to McDermott v. Wisconsin, 228 U.S. 115 (1913), essentially the first FDCA successful preemption case ever, it has been established that a product, labeled in compliance with FDA regulations (although in 1913, it wasn't the FDA yet), and traveling in interstate commerce, cannot be excluded by state law.  In McDermott the Court recognized the preemption of a state statute that prohibited any product – including products labeled in accordance with the FDCA – unless they carried a state-specific label that was inconsistent with federal law.  The Supreme Court barred the state from prohibiting importation and sale of the federally-approved product:

If truly labeled within the meaning of the [predecessor of the FDCA], his goods are immune from seizure. . . . [T]he Wisconsin statute provides that they shall bear the label required by the state law and none other. . . . . In others words, it is essential to a legal exercise of possession of and traffic in such goods under the state law that labels which presumably meet with the requirements of the Federal law, and for the determination of the correctness of which Congress has provided efficient means, shall be removed from the packages before the first sale by the importer. . . . Conceding to the state the authority to make regulations consistent with the Federal law for the further protection of its citizens against impure and misbranded food and drugs, we think to permit such regulation as is embodied in this statute is to permit a state to discredit and burden legitimate Federal regulations of interstate commerce, to destroy rights arising out of the Federal statute which have accrued both to the government and the shipper, and to impair the effect of a Federal law which has been enacted under the Constitutional power of Congress over the subject.

* * * *

. . .The legislative means provided in the Federal law for its own enforcement may not be thwarted by state legislation having a direct effect to impair the efficient exercise of such means. For the reasons stated, the statute of Wisconsin, in forbidding all labels other than the one it prescribed, is invalid.

288 U.S. 133-34, 137.

So what happened in McCormack?  The state of Idaho passed a "fetal pain" statute limiting abortions to the first 20 weeks of pregnancy.  Apparently an ordinary termination was beyond this particular plaintiff's means.  2012 WL 3932735, at *1.  However, plaintiff "learned that medications inducing abortions had been approved for use in the U.S. and could be purchased over the internet."  Id.  That's exactly what she did.  Somehow, the opinion doesn't give details, the plaintiff "ingest[ed] one or more medications she reasonably believed to have been prescribed by a health care provider practicing outside" the state.  Id., see id. (plaintiff "reiterated that the medications were prescribed by a physician").  These unidentified medications – prescribed by a physician – induced an abortion/miscarriage.  Id.

That abortion, however, was illegal under state law, and plaintiff was threatened with prosecution for using the drugs, albeit as prescribed, in that fashion.  Id. at *2-3.

The rest of the McCormack opinion is devoted to constitutional arguments concerning state restrictions on abortions.  That's not germane to this blog.  But one other aspect of the decision caught our eye:

In addressing [defendant's] argument, the district court stated that, [plaintiff] "clarified at oral argument that the FDA-approved medication she procured through the internet was prescribed by a physician." . . . The district court's findings of fact, namely that [plaintiff] received from a physician FDA-approved medication used to induce an abortion, were not clearly erroneous. These facts were offered in both [plaintiff's] declaration and her complaint. [Plaintiff] stated in her declaration that the medication was "approved for use in the United States". . . . In her complaint, [plaintiff] stated that "physicians providing abortion services in the United States often prescribe medications approved by the U.S. Federal Drug Agency ("FDA") to cause women to abort their pregnancies medically, i.e., non-surgically.". . . . Here, prosecuting attorney [defendant] did not offer any controverted affidavits as to whether the pills were obtained from a physician over the internet or whether they were FDA-approved.

McCormack, 2012 WL 3932735, at *9 (our emphasis added; other emphasis removed).

Thus, as far as we can tell, in McCormack the plaintiff was threatened with state prosecution for using an FDA-approved (and presumably duly labeled) prescription drug in accordance with a physician's prescription.  In other words, the state was seeking to ban the use of an FDA-approved prescription drug.  We don't know for sure whether the use is on- or off-label, but we don't think that matters much since the Supreme Court has held that "off-label" usage . . . for some other purpose than that for which [the product] has been approved by the FDA is an accepted and necessary corollary of the FDA's mission to regulate in this area without directly interfering with the practice of medicine."  Buckman Co. v. Plaintiffs Legal Committee, 531 U.S. 341, 350 (2001) (citation omitted).

Now, we don't doubt that all states can regulate physicians, and thus can regulate the ability of physicians to prescribe off-label.  Thus we have no preemption-related quarrel with Planned Parenthood of Cincinnati Region v. Strickland, 531 F.3d 406 (6th Cir. 2008), allowing a state to do precisely that in the abortion context.  However, the state in McCormack didn't do that – it didn't go after the physician, but rather after the purchaser/user of the drug  – who according to the (rather limited) facts, took the drug as prescribed.  As a conceptual matter that's hard to distinguish that from what the First Circuit did in Bartlett v. Mutual Pharmaceutical Co., 678 F.3d 30 (1st Cir. 2012) – hold that a plaintiff can prevail on a purported state-law duty that the defendant drug manufacturer must remove its properly labeled, FDA-approved product from the market altogether in that state.

Practically every other court to consider that issue – in the common-law context – has held that removal from the market claims are preempted.  States simply can't prohibit the marketing and use of FDA-approved drugs.  See, e.g., Smith v. Wyeth, Inc., 657 F.3d 420, 423 (6th Cir. 2011), cert. denied, 132 S. Ct. 2103 (2012) (rejecting "failure-to-withdraw" argument); Mensing v. Wyeth, Inc., 658 F. 3d 867, 867 (8th Cir. 2011) (vacating earlier opinion to the extent that it embraced the "failure-to-withdraw" theory); Moore v. Mylan, Inc., 840 F. Supp.2d 1337, 1352 n.14 (N.D. Ga. 2012) ("any such state law duty [to cease marketing a drug] would directly conflict with the federal statutory scheme in which Congress vested sole authority with the FDA to determine whether a drug may be marketed in interstate commerce"); Jacobsen v. Wyeth, LLC, 2012 WL 3575293, at *9 (E.D. La. Aug. 20, 2012) ("If state law could require a generic drug manufacturer to wholly withdraw from the market based on the unreasonable danger of the product (which is all a successful failure to withdraw from the market claim could be), it necessarily must repudiate the label approved by the FDA"); Strayhorn v. Wyeth Pharmaceuticals, Inc., ___ F. Supp.2d ___, 2012 WL 3261377, at *16 (W.D. Tenn. Aug. 8, 2012) (holding failure to withdraw claims "invalid" and preempted); Aucoin v. Amneal Pharmaceuticals, LLC, 2012 WL 2990697, at *9 (E.D. La. July 20, 2012) ("[t]o require a generic manufacturer to remove a drug from the market would repudiate the label approved by the FDA"); In re Darvocet, Darvon & Propoxyphene Products Liability Litigation, 2012 WL 2457825, at *1 (E.D. Ky. June 22, 2012) (refusing to follow Bartlett and rejecting "failure-to-withdraw" theory); Johnson v. Teva Pharmaceuticals USA, Inc., 2012 WL 1866839, at *5 (W.D. La. May 21, 2012) (rejecting "failure to withdraw argument"); Eckhardt v. Qualitest Pharmaceuticals, Inc., ___ F. Supp.2d ___, 2012 WL 1511817, at *6 (S.D. Tex. April 30, 2012) (a state law requirement that the drug be completely withdrawn from the market, based solely on a theory that the federally mandated label was inadequate, would also impermissibly conflict with federal law and be preempted"); Fulgenzi v. PLIVA, Inc., ___ F. Supp.2d ___, 2012 WL 1110009, at *7 n.5 (N.D. Ohio March 31, 2012) ( "failure-to-withdraw" theory preempted); Metz v. Wyeth, ___ F. Supp.2d ___, 2012 WL 1058870, at *4 (M.D. Fla. March 28, 2012) (removal from market claim preempted); Cooper v. Wyeth, Inc., 2012 WL 733846, at *6 (M.D. La. March 6, 2012) ("[i]f state law could require a generic drug manufacturer to wholly withdraw from the market based on the unreasonable danger of the product (which is all a successful failure to withdraw from the market claim could be), it necessarily must repudiate the label approved by the FDA"); In re Darvocet, Darvon & Propoxyphene Products Liability Litigation, 2012 WL 718618, at *2-3 (E.D. Ky. March 5, 2012) ("that [defendants] should have simply stopped selling [the drug] is an oversimplified solution"); Bowman v. Wyeth, LLC, 2012 WL 684116, at *6 (D. Minn. March 2, 2012) (rejecting "failure-to-withdraw" theory); Moretti v. PLIVA, Inc., 2012 WL 628502, at *5-6 (D. Nev. Feb. 27, 2012) (liability for "continued distribution" held preempted); Lyman v. Pfizer, Inc., 2012 WL 368675, at *4 (D. Vt. Feb. 3, 2012) (allegation that defendant "could have simply stopped selling the product" held preempted); Coney v. Mylan Pharmaceuticals, Inc., 2012 WL 170143, at *5 (S.D. Ga. Jan. 19, 2012) ("Finding that state law prohibits [defendant] from doing what federal law explicitly requires [defendant] to do would be tantamount to conferring supremacy upon the state law"); Fullington v. PLIVA, Inc., 2011 WL 6153608, at *6 (E.D. Ark. Dec. 12, 2011) (removal from market claim preempted); Gross v. Pfizer, Inc., 825 F. Supp.2d 654, 659 (D. Md. 2011) ("no state law duty that would compel generic manufacturers to stop production of a drug" could "exist, as it would directly conflict with the federal statutory scheme in which Congress vested sole authority with the FDA to determine whether a drug may be marketed in interstate commerce"); In re Reglan Litigation, 2012 WL 1613329 (N.J. Super. Law Div. May 4, 2012) ("conflict between state and federal law would be much more pronounced if the state courts upheld a decision that an FDA-approved drug should not have been on the market").

Since federal power to permit the marketing – and thus the purchase and use – of FDA-approved prescription drugs is necessarily supreme over state power to prohibit such marketing and use, as the above precedent abundantly holds, then the state source of power is irrelevant.  State legislation purporting to ban the marketing of an FDA-approved product (what the Supreme Court held preempted in McDermott back in 1913) is just as preempted as a tort claim ostensibly raising a common-law duty to do the same thing.

Thus, when we see the state in McCormack threaten to prosecute the user of an FDA approved drug for a prescribed use of that drug (not diverting the drug to some non-prescribed purpose, which would not raise any preemption question), we have to say "hold on."  Interstate commerce in prescription drugs, once they're approved by the FDA, can't be prohibited by state law.  States can regulate physicians all they want, but once they go beyond that to the sale and prescribed use of FDA-approved drugs, well, we think there's a bit of a Supremacy Clause problem there.



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Posted By Bexis to Drug and Device Law at 9/28/2012 12:00:00 PM

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Please contact lina@tansoncorp.com for more info.

Job Title: HIE Analyst/Programmer
Job Location: Rochester, MN
Job Duration: 06 Months(contract)
Pay Range: Open

Job Description:
Client is seeking a Health Information Exchange (HIE) Analyst
Programmer for a 6-month contract to assist in connecting EMRs to an
enterprise HIE.
Analyst will have primary responsibility of gathering requirements and
developing/testing interfaces.
Must have the ability to communicate with both technical and non-
technical individuals and be able to translate needs, ideas and
suggestions into logical solutions that interconnect systems.
Will work onsite at Rochester, MN.

Required/Desired Skills:-
* Hands experience in implementation of interfaces to EMR systems 5
Years
* Implementation of HL7 Interfaces 5Years
* Web service development, SOAP, javascript and XML 5 Years
* Mirth, NwHIN, XDS.b, XDS.l SQL Highly desired 1 Years
* C# and/or Java programming 5 Years

Please complete the following and send back with your updated resume.
Full Name:
Hourly rate:
Day Phone #:
Evening Phone #:
Cell Phone #:
Availability:
Current City/State:
Work Status (US Citizen / Green Card / Others):


Tanson is EOE/AA

Tanson Corp. is a Minnesota based Technology Company offering
competitive services in IT consulting and staff augmentation,
providing technology staffing, consulting, and project-based services
in onsite, offsite and offshore environments. To view all our
positions take a look at "Careers" at www.Tansoncorp.com

Follow us:
www.facebook.com/TansonCorp
twitter.com/#!/tansoncorp
www.linkedin.com/company/tanson-corp

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Hello, Greetings from DOTS TECHNOLOGIES INC!! I would like to introduce myself as Manideep from DOTS TECHNOLOGIES INC, located at Piscataway NJ I have a 12 Months opportunity that is Sr Adobe Flex UI Developer @ San Jose, CA.. Please review the details below, if interested reply with your current word formatted resume and contact details and I will call you to discuss. Please send Resumes to MANIDEEPDOTS@GMAIL.COM Job Title Sr Adobe Flex UI Developer Experience Level 6+yrs Location San Jose, CA Start Date ASAP Duration 6+ Months   Must Have Skills:

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Send Resumes to adem@vertigonconsulting.com 

 

Position: BA/Guidewire experience.

Location: New Jersey

Duration: Long Term

Must be local or near by Face to face after phone interview

 

The Conversion Business Systems Analyst will perform analysis, design, and testing activities necessary to convert data from legacy applications into the Guidewire applications.

 

Key activities include:

Participate in discovery meetings to gather documentation related to business processes, functional requirements and workflows

Provide technical diagrams, artifacts, mockups, etc., to accompany business requirement documents. Assist programmers in developing UML diagrams, prototypes and pseudo code

Manage and track changes to system requirements throughout the development, testing and maintenance lifecycle, maintaining accurate documentation at all times.

Maintain continuous communication with end user and developers throughout development and testing lifecycle to ensure final product meets requirements and expected outcomes of the customer, to include both functionality and interface.

Assist Quality Assurance team in developing and executing test plan and scripts. Assist in development of end-user manuals and instructional documentation. Develop data pulls using Structured Query Language (SQL)

Work with reporting team to define specific data analysis equations for reporting purposes.

 

REQUIREMENTS:

Experience developing data pulls using Structured Query Language (SQL). Data analysis and data mapping and data flow diagramming experience. Data Conversion experience in a large project effort.

Two years of documented and verifiable experience as a Business Systems Analyst or equivalent role inclusive of writing system requirements.

 

PREFERRED:

Data conversion experience in the insurance industry.

Data cleansing, data transformation and data matching experience.

Data loading experience with tool-based (ex. ETL or EAI) and native data loaders. Experience with Guidewire applications and data structures.

Knowledge of Insurance industry business practices. Experience with Insurance applications.

XML experience

 

Thanks & Regards
 
Adem
Technical Recruiter
Vertigon Consulting
Phone: 201-786-2670
Fax: 732-398-0506
Email: adem@vertigonconsulting.com

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