Job Description

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• Careers in

ICON Careers

We encourage our people to seize the opportunity to bring flexibility, innovation and determination to every situation.

By doing this, our people build exciting and rewarding careers, deliver results to help bring life-changing medicines and devices to market and maintain ICON\'s success as an industry leader.

Full Service

Full-service roles offer the opportunity to work on projects and programmes on behalf of the world\'s most innovative pharma, biotech and medical device companies.

ICON Strategic Solutions

Our Strategic Solutions team is embedded in our clients\' businesses, helping to deliver cutting edge research.

Government and public health services

With our Government and Public Sector Solutions (GPHS) team you could be on the ground helping to resolve a crisis or having an impact on global health issues.

Global Business Services

Global Business Services functions are the backbone of the organisation, providing support services in areas including Finance, IT, HR, Sales, QA, Facilities & Administration, Legal & Procurement.

Commercial roles offer opportunities to be involved in the exciting world of proposals, sales and marketing.

Overview of Service Lines

ICON offers a broad range of specialised services to assist pharmaceutical, biotechnology and medical device companies to bring new drugs and devices to market faster. Our services span the entire lifecycle of product development and can be adapted to suit small local trials or large global programs.

• Our Locations

Our Locations

With headquarters in Dublin, Ireland, ICON has employees in 119 locations across 53 countries.

• Why ICON?

Why ICON?

No matter what part of ICON you work in, you are contributing to solving some of the most complex healthcare challenges and are helping to deliver new medicines and devices that are impacting millions of peoples\' lives, right across the world.

Why icon? full service mean for you?

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Events? full service mean for you?

Integer posuere erat a ante venenatis dapibus posuere velit aliquet. Duis mollis, est non commodo luctus, nisi erat porttitor ligula. * Early Talent

Early Talent

Early talent programs are designed to provide participants with opportunities to gain valuable experience, develop their skills, and build relationships with experienced leaders within the organization. Early talent programs can take many forms, including internships, academy programs, and leadership development programs. ICON is committed to recruiting top talent while also fostering a culture of learning and development within the organization.

graduate What does full service mean for you?

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Clinical Research Associate

• Location:

India

Reference: 2023-105471

• Categories

Clinical Monitoring * __vacancyopjusttionswidget.opt-Business Area__
ICON Strategic Solutions * __vacancyopjusttionswidget.opt-Remote Working __
Remote

About the role

As a (job title) you will be joining the world\xe2\x80\x99s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

What you will be doing:

\xef\x82\xb7 Performing monitoring visits according to plan, document actions and follow up on action plans
\xef\x82\xb7 Site feasibility visits incl. analysis of site logistics, site personnel performance/quality indicators and accountability for patient recruitment strategies
\xef\x82\xb7 Train and guide site staff in the protocol and trial procedures to minimize protocol deviations (PDs)
\xef\x82\xb7 Train site staff in safety information handling and systems
\xef\x82\xb7 Know and meet all local and company requirements with respect to safety reporting
\xef\x82\xb7 Proactive use of EDC and other data source systems for preparation and conduct of site visits as well as source data verification in collaboration with data management/logistics team
\xef\x82\xb7 Identify potential risks and proactively take action to prevent or mitigate
\xef\x82\xb7 Collaborate with Data Management/logistics in resolving queries
\xef\x82\xb7 Ensure data cleaning cycle timelines are met in accordance with the Data Flow Plan
\xef\x82\xb7 Manage trial product requirements, incl. temperature deviations and training of site staff
\xef\x82\xb7 Motivate and build strong relations with site personnel to ensure NN is their preferred clinical research partner
\xef\x82\xb7 Ensure collaboration with and deliverables from vendors locally, if applicable
\xef\x82\xb7 Collection and management of essential documents

You are:

\xef\x82\xb7 Primary point of contact between site staff and NN. Acts as ambassador for the company and contributes to making NN the preferred partner.
\xef\x82\xb7 Responsible for taking leadership of site management for the selection and initiation of sites as well as conduct and closing activities of the appointed studies in compliance with local regulations, ICH-GCP,
\xef\x82\xb7 NN procedures and protocol requirements to ensure data quality and study subject protection.
\xef\x82\xb7 Responsible for managing the site to meet patient recruitment rate and target.
\xef\x82\xb7 Delivers results that have direct impact on the successful completion of the clinical program.
\xef\x82\xb7 Coordinates with PM and communicates to them progress and critical issues that may impair trial progress.

Why ICON?

Our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.

Our success depends on the knowledge, capabilities and quality of our people. That\xe2\x80\x99s why we are committed to developing our employees in a continuous learning culture \xe2\x80\x93 one where we challenge you with engaging work and where every experience adds to your professional development.

ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless \xe2\x80\x93 there\xe2\x80\x99s every chance you\xe2\x80\x99re exactly what we\xe2\x80\x99re looking for here at ICON whether it is for this or other roles.

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Application process

Once you find a job opening that fits your skills and interests, you can create an account, apply and check back on the progress of your application or apply for other roles. Once your application has been received, a confirmation email will be sent to your email.

Remember: this is our first time meeting you. Read the job description and highlight on your CV those experiences that we should learn about.

One of our experienced recruiters will read your profile and determine if you\'re fit for the role and the company. We are aware of instances where fake recruitment text messages and emails that can appear to come from ICON have been received by individuals. Always delete suspicious text messages or emails. Never give out personal financial information.

List #1

Day in the life

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Publish date

08/29/2023

Summary

To excel as a Clinical Research Associate (CRA) in a Clinical Research Organization (CRO), you need a combination of education, skills, and the right mindset. Brazil-based CRA II Debora shares her

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Brazil-based CRA II Debora Oh shares her tips on how to become a great CRA and provides insight into life at ICON.

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Publish date

05/23/2023

Summary

How to progress as a Clinical Research AssociateTo thrive as a Clinical Research Associate (CRA), it is imperative to cultivate a multifaceted skill set and demonstrate unwavering commitment to exce

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Senior CRA Yemi Moses recounts her development and shares her career ambitions with ICON plc.

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Publish date

04/21/2023

Summary

From Clinical Trial Assistant to Clinical Operations Manager, Adrienne Purdy shares her journey.Tell us about you role and what you do at ICON? I have been at ICON since 2013 and I have been growing

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Adrienne Purdy shares her career journey and experience at ICON.

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Adrienne Purdy

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Adrienne Purdy

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