CRA II

ICON Strategic Solutions; Turkey; On-site; EUR 30,000 - 60,000; Full time

Job summary

Join a leading clinical research organization as a CRA II, where your expertise in clinical monitoring and data integrity will play a crucial role in ensuring the highest standards of clinical trials. This position offers the opportunity to work in a dynamic environment that values diversity and high performance. With a focus on employee well-being, you will enjoy competitive benefits and a supportive culture that fosters professional growth. If you are passionate about making a difference in healthcare, this role is perfect for you.

Benefits

Annual Leave

Health Insurance

Retirement Planning

Employee Assistance Programme

Life Assurance

Flexible Benefits

Qualifications

• 2+ years of on-site monitoring experience in clinical trials.
• Fluency in English and host country language required.

Responsibilities

• Conduct onsite and remote monitoring activities per ICH-GCP guidelines.
• Ensure compliance with approved protocols and regulations.

Skills

Clinical Monitoring

ICH-GCP Guidelines

Data Integrity

Report Writing

Negotiation Skills

Education

Bachelor’s Degree in Health Sciences

Job description

As a CRA II you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

What you will be doing:

• Completes onsite and remote monitoring activities in accordance with all ICH-GCP guidelines, applicable regulations, SOPs and study processes
• Verifies the protection of study participants by confirming informed consent procedures and protocol have been performed in accordance to applicable regulations.
• Ensures the integrity of clinical data and that the study is conducted in compliance with approved protocol, GCP, applicable regulations and SOPs.
• Writes and submits reports of investigational site findings and updates applicable tracking systems. Escalates observed deficiencies, issues, and corrective and preventative action plans as appropriate.
• Participates in audit preparation and follow-up activities as needed.
• May serve as preceptor, providing training to less experienced clinical team members.
• May be assigned clinical tasks where advanced negotiating skills are required.

You are:

• Bachelor’s degree in a health, life sciences or other relevant field of study.
• Previous experience supporting clinical trials including 2 years of on-site monitoring experience.
• Travel is required.
• All employees must read, write and speak fluent English and host country language.

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.

#LI-remote

#LI-TS2