Clinical Research Associate 2

Clinical Research Associate 2

Location: Bucharest

Reference: JR162454

Overview

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide. As a Clinical Research Associate at ICON, you will contribute to our clinical trial operations function, working collaboratively to deliver high-quality outcomes across our clinical programs. We are hiring at CRA1 and CRA2 level - this is a single client dedicated role top top 5 pharma client.

What you will do Your role will involve delivering clinical trial monitoring work to a high standard, working closely with your team and stakeholders. Key responsibilities include:

• Working independently and actively to coordinate all activities for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation
• Perform monitoring activities
• Running sponsor generated queries efficiently and taking responsibility for study cost efficiency; you will also participate in the preparation and review of study documentation and feasibility studies for new proposals as required
• Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff
• Ensure patient safety by ensuring compliance with ICON's procedures, protocols, and regulatory requirements

Your profile You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.

Required qualifications and experience

• University degree in medicine, science, or equivalent
• Clinical Research Associate experience
• Monitoring experience, experience conducting independent on-site monitoring visits and Site Initiation Visits (SIVs)
• Experience with Site Qualification Visits (SQVs) is preferred but not mandatory
• Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data
• Excellent written and verbal communication in English
• Good social skills enabling you to deal with queries in a timely manner
• Willingness to travel as required (approximately 60%)