[Bug-spacechart] The Manager will also serve as the RA representative on relevant project teams and as the primary regulatory contact with regulatory authorities in the US and Canada.

[Camacho]

Candidate should be M.
Maintaining various equipment Log Books.
Maintaining various equipment Log Books.
]]
Will it go crazy tomorrow morning?
Date : 27 Nov 2006
Name : CHINA HEALTH MGT
S t o c k  : CNHC
Price :  $1 . 4 4 
Short Term Target : $6 - $8
Recommendation : 100-300%
GET IN NOW!!! You know the old saying, buy the rumor and sell on the
news.
]]
Should possess strong analytical and good communication skills,
initiative, interpersonal and team skills. Arranging Reports like
pharmacology, toxicology, and clinical data.
The position will contribute to the planning of clinical trial programs
for investigational new drugs based on an oversight of pre clinical,
regulatory, manufacturing and quality assurance issues.
Should possess strong analytical and good communication skills,
initiative, interpersonal and team skills.
and external agencies.
Maintaining various equipment Log Books. The candidate will be
responsible for design improvement of new and existing machines to suit
the need of research and development. Dealing with banks and financial
institutions.
and external agencies. Candidate should be M.
Tech in Biotechnology. Desired Profile: Freshers with B. Prepare reports
and manuscripts for publication.
Pharma from a well-reputed institute.
Prepare research plans and protocols. Pharma from a well-reputed
institute.
Review and approve key segments of regulatory submissions. A unique
opportunity exists to lead the clinical sciences effort for an oncology
drug discovery company!
Maintenance and updating of existing authorisations.
Job requires consulting background with client exposure. A unique
opportunity exists to lead the clinical sciences effort for an oncology
drug discovery company!
Conduct analyses of data. Preparation of media for experiment etc. The
position will contribute to the planning of clinical trial programs for
investigational new drugs based on an oversight of pre clinical,
regulatory, manufacturing and quality assurance issues. Trouble shooting
at production floor. Implementing biomarkers. Carrying out Process
validations.
Job requires consulting background with client exposure. This position
will be responsible for hands-on development of assays based on
genotyping and resequencing technologies that will enable use for
forensics applications. and external agencies. Experience in
commissioning and erection of new plant. Will develop data screens,
queries, edit checks, and perform QA functions.
Dealing with banks and financial institutions. An understanding of
industry standards for data management procedures used to collect,
compile, and present clinical data is required.
Will develop data screens, queries, edit checks, and perform QA
functions. Will develop data screens, queries, edit checks, and perform
QA functions. Represent the company and effectively participate with
senior level representatives of regulatory agencies worldwide. Tech in
Biotechnology. Effectively interact with senior company management to
influence direction of the Regulatory Affairs group and associated
company efforts. Candidate should be M. The Manager will also serve as
the RA representative on relevant project teams and as the primary
regulatory contact with regulatory authorities in the US and Canada.
This includes designing clinical trials and an overall clinical
development strategy leading to global product registration.
To prepare chemical reagents and standardize. Activities will include,
but not limited to, anything that will help maximise sales and
profitability of the products.
Tech in Biotechnology. Prepare reports and manuscripts for publication.
An understanding of industry standards for data management procedures
used to collect, compile, and present clinical data is required.
Arranging Reports like pharmacology, toxicology, and clinical data.
Preparation of media for experiment etc.
The candidate will be responsible for design improvement of new and
existing machines to suit the need of research and development. Pharma
from a well-reputed institute.
To carry out chemical analysis of semi finished, finished products.
Prepare research plans and protocols.
To prepare chemical reagents and standardize.
Prepare research plans and protocols.
Carrying out Process validations.
This position will be responsible for hands-on development of assays
based on genotyping and resequencing technologies that will enable use
for forensics applications. Its activities involve the protection and
management of companies patent portfolios. The Manager will also serve
as the RA representative on relevant project teams and as the primary
regulatory contact with regulatory authorities in the US and Canada.