Key Facts

Remote From:

Delaware (USA) , New Jersey (USA) , North Carolina (USA) , Pennsylvania (USA)

Full time

English

Hard Skills

Clinical Study Design Clinical Trial Planning Vendor Management Academic Affairs Office Management Vendor Management Online Communication

Other Skills

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Computer Literacy
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Non-Verbal Communication
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Adaptability
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Multitasking
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Ethical Standards And Conduct
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Time Management
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Teamwork
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Organizational Skills
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Detail Oriented
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Social Skills

Roles & Responsibilities

Bachelor's degree or relevant clinical trial experience
Industry experience in clinical trial support (CRO/Pharma) with a focus on vendor start-up
Experience with vendor management and strong verbal/written communication and organizational skills
Willingness and ability to train others on study administration procedures

Requirements:

Ensure vendor spreadsheets are completed correctly and processed (submitted to vendor or global team) according to study team guidelines
Attend weekly Study Team meetings to report on vendor spreadsheets
Participate in vendor management activities
Support documentation and administrative tasks related to study Start-Up processes

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

Clinical Trial Associate - US (Study Start-Up Support)

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

What you will be doing

The SSU Clinical Study Administrator is responsible for ensuring vendor spreadsheets are completed correctly and processed (submitted to vendor or global team) according to study team guidelines.
SSU CSA will attend weekly Study Team meetings to report on vendor Spreadsheets.
SSU CSA will participate in vendor management activities

Your profile

Bachelor's degree or relevant clinical trial experience
Industry expereince in clinical trial support required (CRO/Pharma) with a focus on vendor support during Start-Up
Experience with vendor management, strong verbal & written communication skills,
and strong organizational skills
Previous administrative experience
Proven organizational and administrative skills
Computer proficiency
Display excellent organization and time management skills, excellent attention to detail, and ability to multi-task in a high-volume environment with shifting priorities
Team oriented and flexible; ability to respond quickly to shifting demands and
opportunities
Working knowledge of the Clinical Study Process and an understanding of the range of working procedures relating to study Start-up, together with an understanding of the ICH/GCP guidelines
Ability to develop advanced computer skills to increase efficiency in day-to-day tasks
Good interpersonal skills and ability to work in an international team environment
Willingness and ability to train others on study administration procedures
Integrity and high ethical standards

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