Messages In This Digest (4 Messages)

1.: What to do when the new job is a nightmare From: Ron Katz

2a.: Re: Networking tips for Extraverts From: R Friedman

3.: Sr. Clinical Study Manager contract in Stamford, CT From: John Barry

4.: Medical Writer contract in Stamford CT From: John Barry

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1.: What to do when the new job is a nightmare

Posted by: "Ron Katz" ronhrkatz@yahoo.com ronhrkatz

Wed Aug 18, 2010 9:11 am (PDT)

A couple of people I have worked with who have landed are coping with the
renewed stress of having and keeping a job. Even if the job is not new, just
stressful, this could help.

Some good tips in the attached link.
Ron

http://cuberules.com/2010/08/16/what-to-do-when-your-new-job-is-a-nightmare/

"The work is never done while the power to work remains." - Oliver Wendell
Holmes
Warning: Dates in calendar are closer than they appear.

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2a.: Re: Networking tips for Extraverts

Posted by: "R Friedman" rfmbacpa@yahoo.com rfmbacpa

Wed Aug 18, 2010 9:32 am (PDT)

Extraverts should be taught the acronym W.A.I.T., Why am I talking? Don't you think?

--- On Tue, 8/10/10, Ron Katz <ronhrkatz@yahoo.com> wrote:

From: Ron Katz <ronhrkatz@yahoo.com>
Subject: [WNO] Networking tips for Extraverts
To: "Westchester Networking Organization" <Westchester_Networking_Organization@yahoogroups.com>
Date: Tuesday, August 10, 2010, 8:45 AM

We read so much about how introverts can network, but what about those extraverts? It can be a challenge for them (us) as well.
Ron

How to Be More Effective: Tips for Extravertshttp://bit.ly/ dlhIu1

"The work is never done while the power to work remains." - Oliver Wendell Holmes
Warning: Dates in calendar are closer than they appear.

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3.: Sr. Clinical Study Manager contract in Stamford, CT

Posted by: "John Barry" John@itechcp.com itechjohn

Wed Aug 18, 2010 10:26 am (PDT)

Title: Sr / Clinical Study Manager

Location: Stamford, CT

Duration: 1 year

Overview

The Clinical Study Manager (CSM) organizes and facilitates the overall
planning, coordination, tracking and general performance of clinical studies
that support the Clinical Development Plan. The CSM is responsible for
ensuring clinical study quality/consistency of performance and in
conjunction with the Clinical Leader and all other Team members is
responsible for overall timeline adherence and performance against plan of
the clinical study. A critical component of the position is the peer
management and/or support of and coordination with contract research
organization personnel (CROs), consultants, contractors, and other
colleagues to ensure adequate resource volume and quality is maintained on
the studies for which the CSM is responsible. At times, business travel will
be necessary

Required Skills and Qualifications

. Demonstrated knowledge of, and competence in, application of FDA/GCP/ICH
guidelines.

. Excellent communication skills, command of medical terminology and of the
application of scientific/medical and clinical concepts used to conduct
Phase I-IV clinical trials.

. Knowledge and ability to effectively manage multi-site clinical trials
with minimal supervision.

. Ability to lead cross functional teams; excellent organization,
negotiation and team motivation skills are essential.

. Ability to multi-task and effectively prioritize in order to ensure
clinical trial goals.

. Ability to successfully manager CROs in a fully outsourced model

Visit www.itechcp.com for more information about our company and a list of
our hot jobs.

Best regards,

John Barry
ITech Consulting Partners
30 Church Hill Road
Newtown, CT 06470
203-270-0051 Ext: 301
203-270-0071 Fax
john@itechcp.com
www.itechcp.com
Providing IT professionals on a contract or fulltime basis.
Please visit our website at www.itechcp.com for more information about our
company and a list of our hot jobs.
linkedin profile: http://www.linkedin.com/in/itechjohn
http://www.facebook.com/pages/Newtown-CT/ITech-Consulting-Partners/500931085
054#!/pages/Newtown-CT/ITech-Consulting-Partners/500931085054?v=wall
www.twitter.com/itechjohn

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4.: Medical Writer contract in Stamford CT

Posted by: "John Barry" John@itechcp.com itechjohn

Wed Aug 18, 2010 10:26 am (PDT)

Title: Medical Writer - Regulatory Medical Research Documents

Location: Stamford, CT

Contract Duration: 1 year

Overview

The individual will serve as the medical writer of regulatory medical
research documents such as clinical study reports and protocols. The work
will involve serving as the link between the Clinical Research Organization
(CRO) medical writers and study team, reviewing and editing the CRO's work,
coordinating all internal comments, and communicating back to the CRO. The
individual will participate in several study teams as the designated medical
writing functional representative and review the work of medical writing
counterpart at the CRO in the preparation of protocols and clinical study
reports; will be the writer of protocols and clinical study reports and will
also post the results on clinicaltrials.gov.

Required Skills and Qualifications:

. Undergraduate degree in science or journalism/English with at
least at least 4 years of experience writing and editing clinical study
reports in a pharmaceutical environment. A graduate degree in science or a
health-related field is highly preferred.

. Excellent oral and written communication skills in presenting
medical research data in fluent English.

. Strong skills in interpreting clinical and statistical data.

. Knowledge of regulatory requirements for clinical study reports
(eg, ICH, FDA).

. Experience managing medical writing deliverables from CROs or
contractors.

. Good interpersonal skills; assignment requires interaction with
internal and external colleagues.

Visit www.itechcp.com for more information about our company and a list of
our hot jobs.

Best regards,

John Barry
ITech Consulting Partners
30 Church Hill Road
Newtown, CT 06470
203-270-0051 Ext: 301
203-270-0071 Fax
john@itechcp.com
www.itechcp.com
Providing IT professionals on a contract or fulltime basis.
Please visit our website at www.itechcp.com for more information about our
company and a list of our hot jobs.
linkedin profile: http://www.linkedin.com/in/itechjohn
http://www.facebook.com/pages/Newtown-CT/ITech-Consulting-Partners/500931085
054#!/pages/Newtown-CT/ITech-Consulting-Partners/500931085054?v=wall
www.twitter.com/itechjohn

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