ICON
is a global provider of outsourced development services to the
pharmaceutical, biotechnology and medical device industries. We
specialize in the strategic development, management and analysis of
programs that support Clinical Development – from compound selection to
Phase I - IV clinical studies
ICON enjoys a strong reputation for quality and is focused on staff development. We make it our mission to attract the most diverse and creative minds into the business and we continually strive to provide opportunities for our people to excel, grow and build a great career. We understand that our greatest asset is the skills and talents of our people and they are truly what set us apart.
ICON enjoys a strong reputation for quality and is focused on staff development. We make it our mission to attract the most diverse and creative minds into the business and we continually strive to provide opportunities for our people to excel, grow and build a great career. We understand that our greatest asset is the skills and talents of our people and they are truly what set us apart.
Post: Clinical Research Associate entry level
Job Description:
You will be responsible for in-house contact and site management for the assigned sites and assist with the follow up and resolution of actions in consultation with CRA. Site management will include communication with the site on recruitment status, follow-up on data entry and queries, obtaining site updates to provide to the project teams and the tracking of discussions.
You will work with the Monitoring CRA to address the Clinical Data Analyst findings.
You will be responsible for the quality and completeness of data in CTMS and the Trial Master File.
You will be responsible for in-house contact and site management for the assigned sites and assist with the follow up and resolution of actions in consultation with CRA. Site management will include communication with the site on recruitment status, follow-up on data entry and queries, obtaining site updates to provide to the project teams and the tracking of discussions.
You will work with the Monitoring CRA to address the Clinical Data Analyst findings.
You will be responsible for the quality and completeness of data in CTMS and the Trial Master File.
To
apply you will need a proven background in Clinical research coupled
with excellent communication and relationship skills. You will be
meticulous and organized and be able to follow an issue to resolution.
You will need to take ownership and accountability for your sites and
deliver to a high standard.
Fluent
in English, as well as the local language, you will possess excellent
written and verbal communication and interpersonal skills enabling you
to deal with queries in a timely manner. You should be able to produce
accurate work to tight deadlines within a pressurised environment.
You
will have the opportunity to progress your career and may wish to move
into CRA monitoring, SSUA Project Management or into other related areas
where you can further develop your skill set.
Additional Information:
Location: Bangalore, Chennai
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: CR
Reference: 015425
End Date: 10th July, 2015
Location: Bangalore, Chennai
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: CR
Reference: 015425
End Date: 10th July, 2015
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