Pharma Tips

Walk-In for CDC I/II/III - Icon Clinical Research India Private Limited

By: Pharma Jobs | Views: 7632 | Date: 15-Jul-2011

"At ICON, it's the people that set us Apart"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

at Chennai/Bangalore/Hyderabad

Summary
 

Experience:

1 - 6 Years

Location:

Bengaluru/Bangalore, Chennai, Hyderabad / Secunderabad, Trivandrum

Education:

UG - Any Graduate - Any Specialization,Graduation Not Required PG - Any PG Course - Any Specialization,Post Graduation Not Required

Industry Type:

Pharma/ Biotech/Clinical Research

Role:

Clinical Research Associate/Scientist

Functional Area:

Healthcare, Medical, R&D

Posted Date:

15 Jul

Desired Candidate Profile

Candidate must have 1-6 years of experience in Clinical Data Validation.
Job Description

Hi,

ICON Clinical is looking for CDC I/II/III to be based in Trivandrum. We are conducting Walk-in interviews in Chennai / Hyderabad / Bangalore/  Trivandrum.

Please call Neil @ +91 8754487013 to get your interview slot in any of those locations.

Please send your resume, current CTC, Expected CTC and Preferred location to attend interview asap.

Below is the JD:

"At ICON, it's the people that set us Apart"

 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.

Description: Role Responsibility

Working within a highly qualified team you will perform data management activities to ensure the generation of accurate, complete, and consistent clinical databases. Fulfilling your job responsibilities in accordance with Good Clinical Practices (GCPs), ICON Standard Operating Procedures (SOPs), Working Procedures (WPs), Study Specific Procedures (SSPs), International Committee on Harmonization (ICH) Guidelines, and all applicable laws and regulations.

Additional Responsibilities:

Working independently and proactively you will Review Case Report Form (CRF) data for completeness, accuracy, and consistency identifying and resolving data discrepancies

Update/correct/review data in the clinical databases based on resolved data queries

Assist with the testing of data entry screens and the preparation of the relevant testing documentation.

Create and maintain study files and other appropriate study documentation

Dependent on level of experience you may assist in training and mentoring less experienced CDC’s.


Experience and Qualification

With a University degree in medicine, science, or equivalent, you will have previous Data Management experience (for all roles above Entry Level). In addition, you will also require:

Knowledge of ICH GCP guidelines and expertise to review and evaluate medical data

Fluency in English


Excellent communication and interpersonal skills, both written and verbal enabling you to deal with queries in a timely manner


Ability to produce accurate work to tight deadlines within a pressurised environment

Computer literate with Microsoft Office

You will have the opportunity to progress your career and may wish to move into Project Management or into other related areas where you can further develop your skill set.

Come to ICON and be an important part of a well respected and growing company that believes the details of your career are every bit as critical as the work you do. You'll enjoy highly competitive compensation and an exceptional benefits package

ICON Clinical Research is an Equal Opportunity Employer committed to strength in diversity.

Keywords: clinical data management,CDM,Data validation,Oracle clinical,RAVE,query editor,data management

Company Profile
"At ICON, it's the people that set us Apart"


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.
Contact Details

Company Name:

Icon Clinical Research India Private Limited

Executive Name:

Neil

Address:

Not Mentioned

Telephone:

+918754487013

Reference ID:

CDC

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