Senior Clinical Associate

ICON Clinical Research; España; A distancia; EUR 28.000 - 42.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Annual leave entitlements

Health insurance

Competitive retirement planning

Global Employee Assistance Programme (

Life assurance

Flexible country-specific benefits

Descripción de la vacante

ICON Strategic Solutions is seeking a Clinical Trial Assistant to join a sponsor‑dedicated model backed by ICON’s global expertise. You will oversee and support trial execution with a strong focus on quality and compliance.

You will coordinate clinical activities, manage site work, collaborate with cross‑functional teams, and help monitor timelines, data integrity, and regulatory adherence to ensure successful study outcomes.

Formación

• Bachelor's degree in a relevant scientific discipline or healthcare-related field.
• Significant experience in clinical trial management and regulatory requirements.
• Ability to manage multiple projects with strong organization and problem‑solving.
• Excellent communication and interpersonal skills with diverse stakeholders.
• Detail‑oriented with proactive approach to trial success.

Responsabilidades

• Managing and coordinating clinical trial activities to ensure adherence to protocols and timelines.
• Collaborating with cross-functional teams to address trial issues and optimize processes.
• Overseeing site management and monitoring for data integrity and regulatory compliance.
• Providing guidance to clinical staff and investigators on best practices and standards.
• Tracking and reporting trial progress, identifying risks, and mitigating challenges.

Conocimientos

Clinical coordination

Clinical trial management

Organizational skills

Problem solving

Communication skills

Educación

Bachelor's degree in a relevant scientific discipline or healthcare-related field

Descripción del empleo

Clinical Trial Assistant

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 a Senior Clinical Associate at ICON, you will oversee and support the execution of clinical trials, ensuring the highest standards of quality, compliance, and efficiency.

What You Will Do:

You will lead on clinical coordination tasks requiring technical depth, with a focus on quality and continuous improvement.

Key responsibilities include:

• Managing and coordinating clinical trial activities to ensure adherence to protocols, regulatory requirements, and project timelines.

• Collaborating with cross-functional teams to address clinical trial issues, optimize processes, and ensure the effective execution of studies.

• Overseeing site management and monitoring to ensure data integrity and compliance with study protocols.

• Providing guidance and support to clinical staff and investigators, ensuring adherence to best practices and regulatory standards.

• Tracking and reporting on trial progress, identifying potential risks, and implementing strategies to mitigate challenges.

Your Profile:

You will have a strong foundation in clinical coordination, with the experience to work independently and guide others.

Required qualifications and experience:

• Bachelor's degree in a relevant scientific discipline or healthcare-related field

• Significant experience in clinical trial management, with a strong understanding of clinical trial processes and regulatory requirements.

• Proven ability to manage multiple projects effectively, with strong organizational and problem-solving skills.

• Excellent communication and interpersonal skills, with the ability to collaborate effectively with diverse teams and stakeholders.

• Detail-oriented with a proactive approach to ensuring trial success and addressing clinical challenges.

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)