Senior Clinical Research Associate
1 month ago
We are seeking a highly skilled Senior Clinical Research Associate to join our team at ICON plc. As a Senior CRA, you will play a critical role in the success of our clinical trials, working closely with our team to identify, select, initiate, and close-out investigational sites.
Key Responsibilities:
- Coordinate activities to set up and monitor studies, ensuring accurate study status reports and maintaining study documentation.
- Submit protocol and consent documents for ethics/IRB approval and assist in preparing regulatory submissions as requested.
- Participate in preparing and reviewing study documentation and feasibility studies for new proposals.
- Balancing sponsor-generated queries efficiently and responsible for study cost-effectiveness.
- Assist in training and mentoring less-experienced CRAs and/or lead CRAs working on international projects.
Requirements:
- 18 months+ of monitoring experience in phase I-III trials as a CRA.
- Knowledge of ICH GCP guidelines and expertise to review and evaluate medical data.
- Excellent written and verbal communication in English.
- Ability to produce accurate work to tight deadlines within a pressurized environment.
- Valid driving license and willingness to travel at least 60% of the time (international and domestic).
What We Offer:
- Competitive salary and benefits package.
- Opportunities for career growth and professional development.
- Collaborative and inclusive work environment.
- Recognition and rewards for high performance.
At ICON plc, we are committed to providing a workplace free of discrimination and harassment. We welcome applications from diverse candidates and are an equal opportunity employer.
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