Senior CRA

ICON Strategic Solutions; Illinois; Remote; USD 80,000 - 100,000; Full time

Job summary

A leading healthcare intelligence and clinical research organization seeks a Senior CRA to join their team. In this role, you will monitor clinical trials, ensure compliance with regulations, and collaborate with biopharmaceutical companies. The ideal candidate has a strong background in life sciences, significant CRA experience, and is fluent in English and Hebrew. ICON offers competitive salaries and a range of benefits focused on well-being and work-life balance.

Benefits

Various annual leave entitlements

Health insurance offerings

Competitive retirement planning

Global Employee Assistance Programme

Life assurance

Flexible optional benefits

Qualifications

• At least 4 years of monitoring experience in phase I-III trials as a CRA.
• Knowledge of ICH-GCP guidelines and ability to review and evaluate medical data.

Responsibilities

• Set up and monitor studies, complete reports and maintain documentation.
• Submit protocol and consent documents for ethics/IRB approval.
• Prepare and review study documentation and feasibility studies.

Skills

Oncology

English

Hebrew

Time Management

Education

Life science / healthcare related degree

Degree in medicine or science

Job description

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.

As a Senior CRA in Israel you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

You will be partnering with one of the worlds premier Biopharmaceutical companies. Working across a vast portfolio of medicines and vaccines this company has, over centuries created a strong heritage of delivering innovative treatments and preventive medicines globally.

• What you will be doing:
  
  • Independent, proactive work to set up and monitor studies, complete reports and maintain documentation
  • Submitting protocol, consent documents for ethics/IRB approval, as well as preparing regulatory submissions
  • Balancing sponsor generated queries
  • Taking responsibility for study cost efficiency
  • Preparation and review of study documentation and feasibility studies for new proposals
  • Potential to assist in training and mentoring fellow CRAs

You are:

• A life science / 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
• Previous monitoring experience in medium-sized studies, including study start-up and close-out
• Oncology experience
• Knowledge of ICH-GCP guidelines and ability to review and evaluate medical data
• Fluency in English as well as Hebrew.
• Ability to work to tight deadlines.
• Availability to travel at least 60% fly and drive and should possess a valid driving license.

#LI-SK1

#LI-remote

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 maximise 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 website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits

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, colour, 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 through the form below.

https://careers.iconplc.com/reasonable-accommodations

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.