Global Clinical Trials Coordinator
6 days ago
**Job Summary**
Join our dynamic team as a Clinical Research Associate and play a vital role in delivering high-quality clinical trials within Oncology. As a key member of our global clinical trials team, you will be responsible for monitoring and coordinating trials, mentoring junior team members, and working closely with our country budget development team.
**Responsibilities**
The successful candidate will have:
- Mentor and coach junior team members
- Act as Lead Site Manager, training other Site Managers on study protocols
- Develop site startup documents, including SIV agendas and Monitoring Guidelines
- Take over LTM roles, reviewing reports (SQV, SMV, SCV) for assigned sites
**Requirements**
To succeed in this role, you will need:
- Minimum 2-5 years' experience in monitoring pharmaceutical industry clinical trials
- Minimum 1-2 years' experience monitoring Oncology trials
- Strong analytical and risk-based monitoring skills
- Excellent communication and influencing skills to effectively manage study sites remotely and face-to-face
**What We Offer**
We offer a competitive salary and benefits package, including access to our Global Employee Assistance Programme, flexible country-specific optional benefits, and a range of health insurance options. At ICON, diversity, inclusion, and belonging are fundamental to our culture and values.
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