Monday, April 19, 2010

[SMCNG] Digest Number 369

The St. Matthias Career Networking Group

Messages In This Digest (6 Messages)

Messages

1.

LEAD:  Dir Conf Plng & Events - NJ - Full Time

Posted by: "john sampson" jcsspike@yahoo.com   jcsspike

Sun Apr 18, 2010 1:14 pm (PDT)



 
Director Conference Planning and Events 
Job ID:   27611 
Location:  Piscataway, New Jersey 
Full/Part Time:   Full-Time 
Regular/Temporary:  Regular 
 
About Telcordia 
Telcordia Technologies is a leading global provider of telecommunications software and services for IP, wireline, wireless, and cable networks.  The company delivers flexible, standards-based solutions that optimize complex network and business support systems, enabling customers to manage, transform and grow their businesses. 
 
General Responsibilities 
Establishes operational objectives and assignments and delegates assignments to subordinate managers.  Objectives are reviewed by senior management to determine success of operation.  Generally responsible for the management of an organization unit, including the development and execution of unit initiatives.  Contributes to setting direction and goals of the organization, and functions as an advisor regarding tasks, projects and operations.  Involved in developing, modifying and executing company policies which affect immediate operations and may also have company-wide effect. Erroneous decisions will result in critical delays in schedules/operation s and may jeopardize overall business activities.  Manages work through professional staff.  This is considered the first "true" level of management with full accountability for all human resource decisions.  Generally has full budget and management responsibility.  Normally has technical knowledge
and skill set equivalent to a G level professional or greater.  Typically requires 10+ years of related experience with a BS; 6+years of experience with an MS.  Strategic advisor to senior management on communication issues.  Represents company/department view to key audiences.  Has broad understanding of corporate business strategies and goals, and is able to plan/direct within dynamic situations. 
 
Major Duties & Functions 
 - Responsible for strategic planning and execution of all internal and external events, conferences and trade shows worldwide with the goal of establishing and maintaining stakeholder relations to achieve a favorable image of the company with customers, potential customers, employees and the general public. 
- Oversight of all aspects of Customer Briefing Center, including scheduling, planning and technical support for customer and sales meetings, conferences and technical demonstrations of software products and solutions.
- Consults with executive leadership, business units, sales, and corporate to communicate corporate and marketing messages to target audience(s).
- Interface with business unit representatives and sales teams to plan and executive customer facing and industry marketing events and activities worldwide.
- Has understanding of corporate business strategies and goals, and is able to plan/direct within dynamic situations
- Collaborate with brand manager and marketing teams for the production of all event production assets, including: theme, logo, ads, posters, banners, video, and stage materials, among others
- Manages two full-time employees and one part time contractor.
- Manages external agencies to execute program elements as needed.
- Full budget and management responsibility 
 
Qualifications You Must Have 
 - Excellent written communication skills
- Analytical skills
- Problem solving skills
- Highly organized and detail oriented
- Strong multi-tasking skills
- Strong computer and technical skills
- Willingness to travel as needed (~50%)
- Bachelor's degree in Marketing, Event Planning, Communications, or related field
- 10+ years relevant experience in the events marketing industry with emphasis on tradeshow planning and corporate theater production
- Technical acumen in AV equipment and presentation technologies
- Technical acumen in graphics and presentation production software such as Photoshop, Illustrator and PowerPoint 
 
 Additional Qualifications 
 - Strong leadership, interpersonal  and time management skills
- Strong project management skills
- Ability to think strategically and creatively
- Excellent oral and written communication skills
- Ability to multi-task in a fast paced dynamic environment
- Ability to manage multiple agendas; prioritize assignments and people
- Excellent prioritization skills with a clear focus on results.
- Demonstrated problem solving ability, including strong conceptual and analytical skills and ability to turn findings into executable plans.
- Ability to delegate effectively, work independently, and in group settings
- Knowledge of computer networking infrastructure 
 
 Relocation Benefits 
 This position is eligible for relocation assistance. 
 
 Equal Employment Opportunity 
 Telcordia Technologies is an Equal Opportunity/ Affirmative Action Employer. 
 
 How To Apply 
Apply @ https://careers. telcordia. com/psc/TELCORDI A/APPLICANT_ PORTAL/HRMS/ c/HRS_HRAM. HRS_CE.GBL? JobOpeningId= 27611&SiteId=1&Page=HRS_CE_ JOB_DTL&
 

MIS Ntwk Assoc Mtg Dates:

Apr 20th - Tues - Bring 20 copies of your resume - 6 pm - NEW LOCATION - BERMAN LARSON KANE 12 Route 17 North, Suite 209 Paramus, New Jersey 07652
201.909.0906 - plan to have dinner with us afterwards
May 4th - Tues - Dinner Mtg - Holiday Inn Totowa - Ed Steinberg - LinkedIn
2.

Permanent job of Sr. Study Data Manager in NJ

Posted by: "Rich Pettus" richpettus@gmail.com   rich.pettus

Sun Apr 18, 2010 1:14 pm (PDT)



Hari P<http://www.linkedin.com/profile?viewProfile=&key=15792213&authToken=DHih&authType=name>

Lead Scientific Recruiter at Makro Scientific

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Permanent job of Sr. Study Data Manager in NJ

Incumbent is required to have a Bachelor's Degree in a health science or
Informatics, and a minimum of 5 years of experience, of which at least 2
years were as a Data Coordinator; or equivalent.
Prior experience with oncology is strongly preferred.
Experience includes a understanding of medical terminology, disease states,
encoding systems (i.e. MedDRA, WHO-DD, microorganism classification, etc.)
and an understanding of regulations and guidelines (i.e. ICH, GCP, European
Clinical Trials Directive, Privacy rules [HIPPA]).
A basic understanding of database theory and experience in using data
management methodologies and technologies (e.g. data computerization,
storage and retrieval methods, electronic data capture) in the set-up,
conduct and closeout of clinical studies is required.
Working knowledge of at least one industry-relevant relational database
application/CDMS (e.g., ClinTrial, Oracle Clinical, etc.) and/or EDC
application is required.
Demonstrated use of at least one data review tool/programming language
(e.g., SAS, PL/SQL, SQLPlus, iReview/jReview) for development and generation
of data listings, ad hoc queries, data tabulations and status or system
reports is desired. Incumbent must understand information flows in clinical
development.
Effective oral and written communication skills are essential.
Incumbent must possess excellent interpersonal relationship skills and be
able to interact with individuals across all levels of Global Clinical
Organization, Medical, Statistics, and the global community in order to
successfully complete assignments.

Contact Info
Hari
973-481-0100 Xt 3051
narahari.pulikollu@makroscientific.com
3.

VP, Compliance Surveillance Business Analyst - New York, NY

Posted by: "Rich Pettus" richpettus@gmail.com   rich.pettus

Sun Apr 18, 2010 1:15 pm (PDT)



[image: Les Jones]<http://www.linkedin.com/profile?viewProfile=&key=18580546&authToken=UEvZ&authType=name>
Les Jones<http://www.linkedin.com/profile?viewProfile=&key=18580546&authToken=UEvZ&authType=name>

VP, Financial Services at International Market Recruiters (Open to Referrals
/ Respects Confidentiality)

See all Les's activity
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VP, Compliance Surveillance Business Analyst - New York, NY

$120,000 - $140,000 + Bonus

Also have opportunities at the Associate Level ($80,000 - $115,000)…

Our Client a Top Tier Investment Firm is looking for a Solid Candidate to
handle a Vice President Level Business Analyst role within their Compliance
Surveillance Strategies Group. Will design and develop complex, profile
based, surveillances with a strong emphasis on the analytical models that
are used for information breach surveillance e.g. insider trading. Lead
global Compliance initiatives focused on business process restructuring
(group performs business analysis functions and in doing so, the group works
closely with Compliance Senior Management, Compliance Officers, Business and
Technology organizations to define, prioritize and lead various initiatives.
The Business Analyst will be responsible for management of surveillance
design and business process restructuring projects. Work with project
sponsors to define and actively mange project scope, plan, resource, budget,
timeline, deliverables and dependencies. Communicate with Key stakeholders
on progress of the project. Analyze surveillance and business issues and
develop creative solutions. Work with the team to apply statistical concepts
/ models to surveillance design across all product types such as equity,
fixed income, credit derivatives and structured. Define criteria for
technology automations, write detail technology specification and work with
technology and compliance teams to implement final solutions.

8+ years Relevant Experience
Ability to Communicate Effectively with Management (Verbal & Written)
Client Service Experience
Project Management Experience Including Experience Managing a Project Team

Also, just so you fully understand how I run my recruitment desk, I do
things strictly confidentially, which means I will NOT send out your resume
without your permission. I will run my client's name and job description by
you first to see if you have either interviewed or have been presented
there, but more importantly, that you would want to go there. If my client
wants to meet you, I will then bring you into my office prior to go over the
interview process and to give you all the information needed to go on the
interview and get the job.
____________________________

The Market is currently on the UP Tick and we are getting plenty of Job
Orders. That being said, if you know someone currently looking have them
reach out to me. Any referrals would be greatly appreciated!

We have an Excellent Understanding and Knowledge of how many Firms Function
from both an Operational and Product Prospective. This grasp of the
Marketplace cuts Valuable Time in the Recruiting Process for Human
Resources, Line Managers and Prospective Candidates.

Thanks,

Les Jones
Vice President
International Market Recruiters
55 West 39th Street, 9th Floor
New York, NY 10018
212.819.9100
551.208.4613 (voicemail)
lcj@goimr.com
4.

Fwd: Administrative Assistant. BofA, Jersey City, NJ

Posted by: "Rich Pettus" richpettus@gmail.com   rich.pettus

Sun Apr 18, 2010 1:17 pm (PDT)



---------- Forwarded message ----------
From: <jcmiao@aol.com>
Date: Sat, Apr 17, 2010 at 10:56 PM
Subject: Career Forum Administrative Assistant. BofA, Jersey City, NJ
To: PSGCNJ@yahoogroups.com

Administrative Assistant - Jersey City, NJ
1000020924
US-NJ-Jersey City

Description

Responsibilities/Position Summary:

Work proactively to support the Managing Director within the
Senior level interaction (both internal and external)
Scheduling conference calls and meetings nearly every day.
Poised, polished and professional
Complex calendar maintenance
International & domestic travel arrangements
Comfortable working with Excel for data maintenance and various project work

Interaction with all levels of executive management, support staff, clients,
etc. with strictest confidence, professionalism and respect

Qualifications
Professional positive attitude and appearance
Articulate - excellent verbal and written communication skills
Excellent phone etiquette
Ambitious and assertive
Self-guided
Ability to work independently with strong administrative/problem solving
skills
Highly organized and able to prioritize
Ability to multi-task in a highly visible fast-paced, team-oriented
environment
Attention to detail
Ability to interface with all levels of Executive Management
Ability to handle confidential matters and information
Proficient in Microsoft Outlook, Word, Excel. PowerPoint is a plus

Apply Now For `Administrative Assistant - Jersey City, NJ`. If you have any
difficulties, refer to the below alternatives. Opens in a new window.

Location: US-NJ-Jersey City
Job Family: A-Administration
Language:
Travel: No
Posting Date: Apr 15 2010
Unposting Date: Apr 30 2010
Hours Per Week:40.00
Full / Part-time: Fulltime-Regular
Shift: 1st Shift
Weekly Schedule:

Apply @
http://careers.bankofamerica.com/JobDetails.aspx?SearchPage=ASP&CountryId=1&JobId=1000020924&stateid=-1&cityid=-1&travel=-1&jfamily=&lang=&fullpart=&shift=&datepost=0&keywords=&jobareas=-1|-1&feedname=BOAFEEDUSA&BOAFeedName=&jobfamilyid=0&internationalcity=&LocationID=0&src=JB-11684<http://careers.bankofamerica.com/JobDetails.aspx?SearchPage=ASP&CountryId=1&JobId=1000020924&stateid=-1&cityid=-1&travel=-1&jfamily=&lang=&fullpart=&shift=&datepost=0&keywords=&jobareas=-1%7C-1&feedname=BOAFEEDUSA&BOAFeedName=&jobfamilyid=0&internationalcity=&LocationID=0&src=JB-11684>

__
5.

Urgently Needed Clinical Scientist, Collegeville, PA

Posted by: "Rich Pettus" richpettus@gmail.com   rich.pettus

Sun Apr 18, 2010 1:17 pm (PDT)



[image: Hemant Singh]<http://www.linkedin.com/profile?viewProfile=&key=35429246&authToken=stR-&authType=name>
Hemant Singh<http://www.linkedin.com/profile?viewProfile=&key=35429246&authToken=stR-&authType=name>

Associate Executive - US Staffing at Artech Information Systems, NJ

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Urgently Needed Clinical Scientist, Collegeville, PA

A Medical Pharmacovigilance Scientist applies his/her skills, knowledge, and
experience to contribute to the overall safety surveillance of marketed and
investigational products. The principle responsibilities of this position
include identification of safety signals, thorough evaluation and analysis
of safety data, and communication of pertinent safety information with
recommendations to Sr. Management The MedPv Scientist performs periodic
aggregate reviews of safety data to identify and analyze safety signals.
He/she plans the approach to the review of complex safety issues with input
from supervisor.
He/she clearly communicates (written and/or verbal) interpretation of safety
signals and recommends action to resolve safety issues. He/she participates
in safety review team meetings by preparing and/or contributing to meeting
materials such as draft discussion documents and line listings. The MedPv
Scientist: Plans and writes draft responses to ad hoc safety queries. .
Plans and writes draft, Periodic Safety Update Reports (PSURs), expert
reports, topic reviews and justification documents. .
Contributes to expert reviews and the development of risk management plans,
and other documents or assignments as required. Ensures documents are
scientifically accurate, and meet company and regulatory standards The MedPv
Scientist assists the manager in the day-to-day surveillance activities of
assigned products, pertinent safety issues and provision of safety reports
within the specific therapeutic area. The MedPv Scientist receives input
from all other MedPv personnel, GSSE senior management, other Pharmaceutical
organizations and affiliates, external healthcare professionals, and
regulatory agencies.

Minimum Requirements BS in Health Sciences (HS) preferred; 5+ years clinical
exp or relevant work exp; pharma required, safety preferred. MS in HS; 3+
years clinical exp or relevant work exp; pharma required, safety preferred.
Pharm D w/ 1+ years clinical exp; pharma required, safety preferred.

Posted 2 days ago | Expiring in 11 days | Reply
Privately<http://www.linkedin.com/groupMsg?displayCreate=&contentType=MEBC&connId=35429246&groupID=2541&goback=%2Eand_2541_17753775_*2_1>

Comments (1)

1. [image: Hemant
Singh]<http://www.linkedin.com/profile?viewProfile=&key=35429246&authToken=stR-&authType=name>
Hemant Singh<http://www.linkedin.com/profile?viewProfile=&key=35429246&authToken=stR-&authType=name>

Associate Executive - US Staffing at Artech Information Systems, NJ

See all Hemant's activity
»<http://www.linkedin.com/groups?viewMemberFeed=&gid=2541&memberID=35429246&goback=%2Eand_2541_17753775_*2_1>

Follow Hemant<http://www.linkedin.com/groupfollowing?follow=&followee=35429246>
Please email me your resume at Hemant_Panwar@artechinfo.com if you'd like
to apply for this job.
6.

CHEMIST - LIMS

Posted by: "Rich Pettus" richpettus@gmail.com   rich.pettus

Sun Apr 18, 2010 1:17 pm (PDT)



Leah Lane<http://www.linkedin.com/profile?viewProfile=&key=45415154&authToken=Guh_&authType=name>

Talent Acquisition Manager at SGS

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CHEMIST - LIMS

SGS is the world's leading inspection, verification, testing and
certification company. Recognized as the global benchmark for quality and
integrity, we employ over 55,000 people and operation a network of more than
1,000 offices and laboratories around the world. In North America, SGS has
over 6,000 employees in over 30 locations.
Our Oil, Gas and Chemical Services, a Division of SGS is looking for two
Analytical Chemists, who have hands on working experience with LIMS, ASTM
testing systems and is IT savvy. Locations are in St. Rose, Louisiana and
Bayonne, New Jersey.

These individuals will be responsible for assisting with the implementation
and training of our internal "SLIM" (LIMS) to our laboratories, across
United States. This is an excellent opportunity for a Chemist that is IT
savvy and willing to travel up to 70% of the time, during the first year of
the new SLIM implementation. Candidate will be thoroughly trained.

o Co-partner with work teams of superuses, IT personnel and laboratory staff
to implement the SLIM program across North America.
o Teach end-users of the LIMs program how to use the new SLIM application
for all the test-methods in their labs and provide continued remote
support.
o Computer literate with good understanding of calculation analysis, and
general knowledge of networks, databases, file transfers and reporting
software.
o Proficient in laboratory work including linking instruments to LIMS,
setting-up program and data files, data transfer, checking formulas and
calculations.
o Analyze results for QA/QC monitoring, replications, round-robin programs,
etc., as required by published methods and SGS qualify standards.
o Able to understand and perform operations on the computer such as to move
/ rename files and folders, save/store data, download and process instrument
data.

Degree in Chemistry or other science area. Should have a minimum of up to
two (2) years of laboratory experience and have hands-on LIMS
instrumentation experience. Should be knowledgeable in laboratory sample
testing methods such as ASTM, API, UOP, etc., and use of instrumentation
such as Karl Fischer, UV, IR, AA, GC, ICP, etc., including reporting and
rounding formats and able to perform majority of petrochemical tests.

Must have excellent communication and presentation skills, coupled with
outstanding Customer Service attitude. Must be able to travel (by air) for
business multiple days per trip as necessary to fulfill SLIM implementation
and schedule requirements during initial launch (18 months), thereafter,
when needed.
Excellent salary and benefit package which includes paid vacation, sick,
holidays, retirement plan, medical, dental, vision, life insurance and
prescription plan. SGS is a drug free work environment and Equal Opportunity
Employer.
Apply at our website:
http://www.us.sgs.com/careers_us<http://www.linkedin.com/redirect?url=http%3A%2F%2Fwww%2Eus%2Esgs%2Ecom%2Fcareers_us&urlhash=ie01>

• Click on "Career Opportunities in United States"
• State: Select the state "New Jersey or Louisiana"
• Business Line: Select Oil, Gas and Chemicals Services
• Functional Area: Leave all selected
• Click on Search "50" and all openings will appear
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