Key Facts

Remote From:

Full time

English

Hard Skills

Clinical Data Analysis Clinical Trial Management Systems Analytics Regulatory Compliance Active Safety Feasibility Studies Stakeholder Communications Cost Management Data Collection Clinical Documentation Database Tuning Online Communication

Other Skills

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Non-Verbal Communication
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Relationship Building
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Teamwork
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Social Skills

Roles & Responsibilities

University degree in medicine, science, or equivalent
Experience as a CRA (minimum 6 months) or Study Coordinator with oncology/hemato-oncology experience
Knowledge of ICH-GCP guidelines and ability to review and evaluate medical data
Ability to travel at least 60% of the time (international and domestic) with a valid driver's license

Requirements:

Coordinate activities for setting up and monitoring a study, complete accurate study status reports, and maintain study documentation
Run sponsor-generated queries efficiently and support study cost efficiency; participate in preparation and review of study documentation and feasibility studies for new proposals
Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff
Ensure patient safety by ensuring compliance with ICON's procedures, protocols, and regulatory requirements

ICON plc

Pharmaceuticals

About ICON plc

Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life. We do this by delivering best in class information, solutions and performance, with an unyielding focus on quality at all times. We offer a full range of consulting, development and commercialisation services from a global network of offices in 53 countries. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost, and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas.

Company type: XLarge

Industry: Pharmaceuticals

Founded: 2018

Company size: 10001

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Job description

POL-CRA II-HB

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development

We are currently seeking a Clinical Research Associate to join our diverse and dynamic team at ICON Plc. As a key member of our research department, you will be responsible for overseeing and coordinating clinical trials, ensuring compliance with regulations, and collecting and analyzing critical data.

What you will be doing

Working independently and actively to coordinate all activities for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation

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

Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff.

Ensure patient safety by ensuring compliance with ICON’s procedures, protocols, and regulatory requirements.

Your profile

University degree in medicine, science, or equivalent
Experience as CRA at least 6 months (this offer can be also applicable for Study Coordinator with oncology or hemato-oncology experience)
Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data
Excellent written and verbal communication in English

Good social skills enabling you to deal with queries in a timely manner

Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid drivers license

#LI-DD1

What ICON can offer you:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs.
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being.
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, 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 or submit a request here.

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Are you a current ICON Employee? Please click here to apply