Clinical Research Associate Lead
Há 7 dias
The Senior Clinical Research Associate will be responsible for coordinating all aspects of the clinical monitoring and site management process in accordance with regulatory guidelines, local regulations and standard operating procedures. This role involves being a decision maker, solving problems independently or as part of the client and ICON team.
This position requires managing competing priorities, supporting the on-site team, ensuring investigators follow the clinical trial protocol, providing training, and motivating the team to ensure high quality results. Key responsibilities include monitoring multiple Phase I, II, III & IV clinical trial sites, across different therapeutic areas, and assisting other CRAs with co-monitoring activities both remote and on-site.
Main Responsibilities:
- Coordinate clinical monitoring and site management processes
- Manage competing priorities and support on-site teams
- Ensure investigator compliance with clinical trial protocols
- Provide training and motivate teams for high-quality results
- Monitor multiple clinical trial sites across various therapeutic areas
- Assist CRAs with co-monitoring activities remotely and on-site
Requirements:
- Bachelor's Degree (or equivalent) with 2-4 years of relevant healthcare experience
- Minimum 6-12 months of monitoring and site management experience
- Scientific background and proficiency with medical terminology
- Working knowledge of Local Regulations and ICH/GCP Guidelines
- Excellent record-keeping skills and attention to detail
- Fluent in English, both written and oral
- Strong technical skills with CTMS, eCRF, eTMF
Benefits:
We offer a competitive salary range of $85,000 - $110,000 per annum, depending on location and experience. Additionally, we provide a range of benefits including various annual leave entitlements, health insurance options, competitive retirement planning, and access to our Global Employee Assistance Programme. We are committed to creating an inclusive and accessible work environment and welcome applications from diverse candidates.
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