Site Budget and Specialist Contract

ICON Clinical Research; Paris; On-site; EUR 45,000 - 65,000; Full time

Benefits offered by this job

Annual leave

Health insurance

Retirement planning

Employee assistance program

Life assurance

Flexible country-specific benefits

Job summary

ICON Clinical Research is seeking an IHCRA (Site Budget and Specialist) to support execution and management of clinical trials in a sponsor-dedicated model. The role emphasizes monitoring deliverables, quality assurance, and collaboration across sites to advance innovative therapies.

The ideal candidate will hold a life sciences degree, possess clinical research exposure, and demonstrate strong organization and communication skills in a fast-paced environment.

Qualifications

• Bachelor's degree in life sciences or healthcare.
• Previous experience in clinical research or a related field preferred.
• Strong organizational and communication skills.
• Ability to work independently and collaboratively in a fast-paced environment.
• Attention to detail and prioritization of tasks.

Responsibilities

• Assisting in the planning, initiation, and execution of clinical trial activities.
• Conducting site feasibility assessments and participating in site selection processes.
• Coordinating with investigative sites to ensure protocol and regulatory compliance.
• Monitoring study progress and data collection to ensure quality and accuracy.
• Assisting in the preparation and review of study documentation and reports.

Education

Bachelor's degree in life sciences

Tools

Clinical monitoring software

Job description

Site Budget and Specialist Contract

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.

As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

As an IHCRA at ICON, you will support the execution and management of clinical trials, contributing to the advancement of innovative treatments and therapies.

What You Will Do:

You will take responsibility for clinical trial monitoring deliverables, applying your skills to ensure quality and efficiency.

Key responsibilities include:

• Assisting in the planning, initiation, and execution of clinical trial activities

• Conducting site feasibility assessments and participating in site selection processes

• Coordinating with investigative sites to ensure compliance with study protocols and regulatory requirements

• Monitoring study progress and data collection activities to ensure quality and accuracy

• Assisting in the preparation and review of study documentation and reports

Your Profile:

You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.

Required qualifications and experience:

• Bachelor's degree in a relevant field, such as life sciences or healthcare

• Previous experience in clinical research or a related field preferred

• Strong organizational and communication skills

• Ability to work independently and collaboratively in a fast-paced environment

• Attention to detail and ability to prioritize tasks effectively

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, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized 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, subsidized travel passes, health assessments, among others.

Visit our careers site (https://careers.iconplc.com/benefits) 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 (https://careers.iconplc.com/reasonable-accommodations)