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ICON plc

Senior Clinical Research Associate

Reposted 2 Hours Ago
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In-Office
Zagreb
Senior level
In-Office
Zagreb
Senior level
Responsible for initiating, monitoring, and closing assigned clinical trial sites, ensuring compliance with regulations and guidelines. Acts as primary contact between site staff and sponsors, conducts feasibility visits, and trains site staff.
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Senior Clinical Research Associate ( Senior CRA) - Remote - Croatia

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

We are currently recruiting for an experienced Senior Clinical Research Associate in Croatia to work on diabetes, obesity, and rare blood and endocrinology studies.

This particular role is a client dedicated one where you will work exclusively on one sponsors trials and SOPs; you will work for a client that values their staff and puts an emphasis on career development.

What you will be doing

  • The Clinical Research Associate is responsible for the initiation, monitoring and closure of assigned sites in clinical studies, in compliance with sponsor's procedural documents, international guidelines such as ICH-GCP, and relevant local regulations and that the sites deliver according to their respective commitment in the individual studies.

  • Primary point of contact between site staff and the sponsor.

  • Performing on-site monitoring visits according to plan, document actions and follow up on action plans

  • Site feasibility visits incl. analysis of site logistics, site personnel performance/quality indicators and accountability for patient recruitment strategies

  • Train and guide site staff in the protocol and trial procedures to minimize protocol deviations (PDs)

  • Collection and management of essential documents

  • Support the site in filing and archiving trial documentation in the Investigator Trial Master File (ITMF)

Your profile

  • Bachelor or master degree in Life Sciences or equivalent

  • 3 years of previous experience as a CRA in independent on-site monitoring of clinical trials

  • Ability to build and maintain relationships with sites

  • High focus on delivery and quality

  • Excellent communication and negotiation skills

  • English verbal and writing skills, e.g. enabling understanding of the protocol and study documents as well as writing monitoring reports

  • Ability to work independently and collaboratively in a fast-paced environment.

  • Ability to travel at least 60% of the time (domestic - fly and drive) and should possess a valid driver’s license

#LI-DS1

#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 maximize 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 site to read more about the benefits ICON offers.

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, color, 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.

Are you a current ICON Employee? Please click here to apply

Top Skills

Clinical Trial Management
Ich-Gcp
Monitoring Systems

ICON plc London, England Office

12 Red Lion Square, Summit House, London, United Kingdom, WC1R 4QH

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