Senior CRA

Pharmaceutical Research Associates, Inc; Turkey; On-site; USD 30,000 - 70,000; Full time

Job summary

Join a leading clinical research organization as a Senior Clinical Research Associate. In this role, you will ensure compliance with ICH-GCP guidelines while conducting onsite and remote monitoring of clinical trials. You will play a crucial role in safeguarding study participants and maintaining data integrity. This innovative firm values high performance and offers a supportive work environment focused on well-being and work-life balance. With competitive salary and diverse benefits, this position is perfect for those looking to make a significant impact in the clinical research field.

Benefits

Annual leave entitlements

Health insurance offerings

Retirement planning offerings

Employee Assistance Programme

Life assurance

Flexible optional benefits

Qualifications

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

Responsibilities

• Conduct onsite and remote monitoring in compliance with ICH-GCP guidelines.
• Ensure integrity of clinical data and participant protection.

Skills

Clinical Monitoring

Negotiation Skills

Report Writing

Regulatory Compliance

Education

Bachelor’s degree in health or life sciences

Job description

Overview

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

Responsibilities

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.

Qualifications

You are:

• Bachelor’s degree in a health, life sciences or other relevant field of study.
• Previous experience supporting clinical trials including 3 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.