ICON Plc Hiring Study Start Up Associate (Clinical Site Activation)
- ICON Plc as a Study Start Up Associate (Clinical Site Activation)
- About ICON Plc
- Job Details
- Key Responsibilities
- Qualifications
- Benefits of Working at ICON Plc
- How to Apply
ICON Plc as a Study Start Up Associate (Clinical Site Activation)
ICON Plc, a leading Clinical Research Organization, is seeking talented Study Start Up Associates (Clinical Site Activation) to join our dynamic team in Sofia, Vilnius, Warsaw, Belgrade, and Tbilisi. If you have a Bachelor’s degree in life sciences and 1-2 years of clinical research experience, this is a fantastic opportunity to advance your career in a supportive and innovative environment.
About ICON Plc
At ICON Plc, we are driven by our mission to improve patients’ lives and deliver excellence in clinical research. Our ‘Own It’ culture is built on four key values: Accountability & Delivery, Collaboration, Partnership, and Integrity. We pride ourselves on fostering a diverse and inclusive work environment where our employees can thrive.
Job Details
Position
Study Start Up Associate (Clinical Site Activation)
Locations
- Sofia, Bulgaria
- Vilnius, Lithuania
- Warsaw, Poland
- Belgrade, Serbia
- Tbilisi, Georgia
Job Type – HYBRID: OFFICE/REMOTE
Experience
Minimum of 1-2 years of clinical research experience
Qualifications
Bachelor’s Degree in life sciences or a related field
Key Responsibilities
As a Study Start Up Associate at ICON Plc, you will:
- Oversee day-to-day execution and site progress for all aspects of site activation for assigned projects and sites.
- Assist and engage with site staff to ensure progress throughout site activation, meeting sponsor timelines and expectations.
- Support internal tool setup, maintenance, and timely updates, ensuring site adoption of ICON tools.
- Contribute to effective site activation processes and timelines.
- Participate in internal study reviews with study teams, contributing to risk identification and action planning.
Qualifications
- Bachelor’s Degree in life sciences or a related field.
- Minimum of 1-2 years of experience in a clinical research environment.
- Project management skills and understanding of regulatory and submission processes in different countries.
- Monitoring experience.
- Excellent English written and verbal communication skills.
- Ability to work to tight deadlines.
Benefits of Working at ICON Plc
Our success depends on the quality of our people. That’s why we offer:
- Competitive Salary Packages: Regularly benchmarked against our competitors.
- Annual Bonuses: Reflecting the delivery of performance goals.
- Health-Related Benefits: For employees and their families.
- Retirement Plans: Including life assurance for long-term security.
- Inclusive Environment: Encouraging a sense of purpose and lasting change.
How to Apply
Interested candidates can apply online at ICON Plc Careers. ICON Plc is an equal opportunity and inclusive employer. If you need reasonable accommodation for any part of the application process due to a medical condition or disability, please let us know.
To apply for this job please visit careers.iconplc.com.
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