Clinical Research Associate (I,II and Senior)
- Poland
- Clinical Monitoring
- ICON Strategic Solutions
- Office Based
Talent Acquisition Business Partner
- Icon Strategic Solutions
About the role
This vacancy has now expired. Please click here to view live vacancies.
As a CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
- Be the go-to expert and main contact for clinical trial sites from start to finish.
- Build strong, lasting relationships with site staff to ensure smooth trial execution.
- Monitor clinical sites to ensure data quality and patient safety in line with GCP and study protocols.
- Master the study protocol and procedures to support site success.
- Drive site readiness by collaborating with cross-functional teams.
- Help identify and validate new study sites.
- Ensure all regulatory and trial documentation is up-to-date and accurate.
- Lead and document site visits (initiation, monitoring, close-out, etc.) with clarity and precision.
- Communicate proactively with investigators about protocol, recruitment, compliance, and performance.
- Coordinate with internal teams and external partners (vendors, IRBs, regulators) to support study milestones.
- Keep systems like CTMS and eTMF accurate and current.
- Support inspections and audits—and even lead them when needed.
- Mentor and co-monitor with peers to share best practices.
- B.A./B.S. preferred with strong emphasis in science and/or biology
Min. 1 year of direct monitoring experience
Previous experience in oncology trials or ready to monitor oncology trials will be an asset
- Fluent in Local Languages and English (verbal and written) and excellent communication skills, including the ability to understand and present technical information effectively
- Excellent understanding and working knowledge of clinical research, phases of clinical trials, current GCP/ICH & country clinical research law & guidelines
- Excellent understanding of Global, Country/Regional Clinical Research Guidelines and ability to work within these guidelines.
- Demonstrated ability to mentor/lead
- Hands on knowledge of Good Documentation Practices
- Proven Skills in Site Management including independent management of site performance and patient recruitment
- Demonstrated high level of monitoring skill with independent professional judgment
- Good IT skills (Use of MS office, use of various clinical IT applications on computer, tablet and mobile devices) and ability to adapt to new IT applications on various devices
- Ability to understand and analyze data/metrics and act appropriately
- Experience with conducting site motivational visit designed to boost site enrollment
- Capable of managing complex issues, working solution-oriented
- Performs root cause analysis and implements preventative and corrective action
Impactful work. Meaningful careers. Quality rewards.
At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential. Learn more about Our Culture at ICON
Day in the life
Teaser label
A Day In The LifeContent type
BlogsPublish date
04/05/2023
Summary
Senior Clinical Research Associate Suzaita Hipolito talks about the satisfaction gained from working in Clinical Research. “What would it look like to wake up every day feeling happy and fulfil
by
Suzaita Hipolito
Teaser label
Career ProgressionContent type
BlogsPublish date
03/20/2020
Summary
Navigating the world of graduate schemes and positions can be daunting, especially if you’re not quite sure of the role or company you want to align yourself with. At ICON, we recognise what a s
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