Clinical Research Associate - Entry level to Senior Openings @ Chennai, Bangalore and Delhi

Clinical Research Associate - Chennai, Bangalore and Delhi

Location Bangalore, Chennai and Delhi

Experience 0 - 4 years

Role Clinical Research Scientist

About Company

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

Job Description

"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.

Job Title: Clinical Research Associate - Entry level to Senior

Role Responsibility

Working within a highly qualified team you will identify, select, initiate and close-out investigational sites for clinical studies in phases II – IV ensuring adherence to applicable regulations and principles of ICG-GCP.

Additional Responsibilities:

* You will work independently and proactively to coordinate all necessary activities required for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation. You will be involved in the submission of protocol, consent documents for ethics/IRB approval and assist in the preparation of regulatory submissions as requested.

* Managing sponsor generated queries efficiently and taking responsibility for study cost effectiveness; you will also participate in the preparation and review of study documentation and feasibility studies for new proposals as required.

* Depending on your level of experience, you may assist in training and mentoring less experienced CRA’s and/or manage CRA’s working on international projects.

Experience and Qualification

* With a University degree in medicine, science, or equivalent; you will have previous monitoring experience in medium sized studies, including study start-up and close-out (for all roles above Entry Level). You should also have knowledge of ICG GCP guidelines and the expertise to review and evaluate medical data.

* 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.

* Computer literate; you will be proficient in Microsoft Office.

* You must be available to travel at least 60% of the time (international and domestic -fly and drive) and should possess a valid driving licence.

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.

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