Senior CRA

Pharmaceutical Research Associates, Inc; Illinois; Remote; USD 60,000 - 100,000; Full time

Job summary

Join a forward-thinking organization as a Senior CRA, where you'll play a vital role in shaping the future of clinical development. This position offers the opportunity to work with leading biopharmaceutical companies on innovative treatments and vaccines. You'll be responsible for setting up and monitoring studies, ensuring regulatory compliance, and mentoring fellow CRAs. With a focus on diversity and inclusion, this company provides a supportive environment that values high performance and personal growth. If you're passionate about healthcare and ready to make a difference, this role is perfect for you.

Benefits

Annual Leave

Health Insurance Options

Retirement Planning

Employee Assistance Programme

Life Assurance

Flexible Benefits

Qualifications

• 4+ years of monitoring experience in phase I-III trials.
• Degree in medicine or science or equivalent work experience.

Responsibilities

• Setting up and monitoring studies, completing reports.
• Submitting protocol and consent documents for approval.
• Managing sponsor-generated queries and ensuring cost efficiency.

Skills

Monitoring Experience

Oncology Knowledge

Fluency in English

Fluency in Hebrew

Knowledge of ICH-GCP Guidelines

Ability to Work Under Tight Deadlines

Education

Life Science Degree

Healthcare-related Degree

Job description

Overview

ICON plc is a world-leading healthcare intelligence and clinical research organization. We foster an inclusive environment that drives innovation and excellence. Join us on our mission to shape the future of clinical development.

As a Senior CRA in Israel, you will join the world's largest and most comprehensive clinical research organization, powered by healthcare intelligence. You will partner with one of the world's leading biopharmaceutical companies, working across a diverse portfolio of medicines and vaccines, with a strong heritage of delivering innovative treatments and preventive medicines globally.

Responsibilities

• What you will be doing:
• Independently setting up and monitoring studies, completing reports, and maintaining documentation.
• Submitting protocol and consent documents for ethics/IRB approval and preparing regulatory submissions.
• Managing sponsor-generated queries.
• Ensuring study cost efficiency.
• Preparing and reviewing study documentation and feasibility studies for new proposals.
• Potentially assisting in training and mentoring fellow CRAs.

Qualifications

• A life science or healthcare-related degree or equivalent work experience.
• At least 4 years of monitoring experience in phase I-III trials as a CRA.
• Degree in medicine, science, or equivalent.
• Experience monitoring medium-sized studies, including start-up and close-out phases.
• Oncology experience.
• Knowledge of ICH-GCP guidelines and ability to review and evaluate medical data.
• Fluency in English and Hebrew.
• Ability to work under tight deadlines.
• Availability to travel at least 60%, with a valid driving license.

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What ICON can offer you

Our success depends on the quality of our people. We prioritize building a diverse culture that rewards high performance and nurtures talent. In addition to a competitive salary, ICON offers various benefits focused on well-being and work-life balance, including:

• Annual leave entitlements
• Health insurance options
• Retirement planning
• Global Employee Assistance Programme (TELUS Health)
• Life assurance
• Flexible country-specific benefits such as childcare vouchers, bike schemes, gym discounts, travel passes, and health assessments

Visit our careers website to learn more: https://careers.iconplc.com/benefits

At ICON, inclusion & belonging are fundamental. We are committed to providing an accessible environment and a workplace free of discrimination and harassment. Qualified applicants will receive equal consideration regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status. If needed, please request reasonable accommodations during the application process at https://careers.iconplc.com/reasonable-accommodations.

Interested but unsure if you meet all requirements? We encourage you to apply—there’s a good chance you are what we’re looking for!