Senior CRA

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

Job summary

An established industry player in healthcare intelligence is seeking a Clinical Trial Monitor to ensure compliance with clinical research protocols. In this role, you will be the primary contact between sponsors and trial sites, overseeing site selection, subject recruitment, and monitoring activities. This position offers a competitive salary and a range of benefits designed to support your well-being and work-life balance. Join a diverse and inclusive team that values innovation and excellence, and make a meaningful impact in the future of clinical development.

Benefits

Annual Leave Entitlements

Health Insurance

Retirement Planning

Employee Assistance Programme

Life Assurance

Flexible Optional Benefits

Qualifications

• Minimum 3 years of independent clinical trial monitoring experience required.
• Good working knowledge of ICH-GCP and local regulations.

Responsibilities

• Serve as a primary contact point between the sponsor and the investigational site.
• Ensure inspection readiness through compliance with protocols and regulations.

Skills

Clinical Trial Monitoring

Good Clinical Practice (GCP)

Communication Skills

IT Skills

Education

BA/BS Degree

Degree in Health or Science

Tools

Clinical Research Protocols

Company Standard Operating Procedures

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.

What you will be doing:

1. Serve as a primary contact point between the sponsor and the investigational site.
2. Be assigned to trial sites ensuring inspection readiness through compliance with the clinical research protocol, company's Standard Operating Procedures (SOP), codes of Good Clinical Practice (GCP), applicable regulations and guidelines from start-up through to data-base lock.
3. Site selection, pre-trial assessment, subject recruitment and retention planning, site initiation, monitoring and close-out.
4. Partnering with the CTA, LTM and GTM to ensure overall site management while performing trial related activities for assigned protocols.
5. May contribute to process improvement and training.

You are:

1. A minimum of a BA/BS degree is required. A degree in a health or science related field is preferred, however, other relevant experiences and skills may be considered by the hiring manager when considering the candidate’s eligibility.
2. A minimum of 3 years of independent clinical trial monitoring experience is required.
3. Good working knowledge of ICH-GCP, company standard operating procedures, local laws and regulations, assigned protocols and associated protocol specific procedures including monitoring guidelines.
4. Good IT skills in appropriate software and company systems. Willingness to travel with occasional overnight stay away from home.
5. Proficient in speaking and writing the country language and English. Good written and oral communication skills.

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:

1. Various annual leave entitlements.
2. A range of health insurance offerings to suit you and your family’s needs.
3. Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead.
4. 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.
5. Life assurance.
6. 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

ICON, including subsidiaries, is an equal opportunity and inclusive employer and 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 or submit a request here.

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.

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