Clinical Associate
hace 2 días
At ICON plc, we are committed to advancing clinical research and providing outsourced services to pharmaceutical, biotechnology, medical device, and government organizations. As a Clinical Associate, you will be an integral part of our study team, acquiring clinical and corporate knowledge of clinical trial conduct. Your primary responsibilities will include providing administrative support to Project Managers, Clinical Trial Managers, and/or sites, with a focus on driving global inspection readiness.
Key Responsibilities:
- Provide administrative support to the study team, including data management, document control, and communication with sites.
- Assist in the development and implementation of global inspection readiness plans.
- Collaborate with cross-functional teams to ensure seamless execution of clinical trials.
Requirements:
- Bachelor's degree in a scientific or medical discipline or equivalent experience.
- Understanding of pharmaceutical industry processes and medical terminology.
- Excellent written and verbal communication skills in English.
Benefits of Working at ICON:
- Comprehensive total reward package, including competitive base pay, variable pay, and recognition programs.
- Best-in-class employee benefits, supportive policies, and wellbeing initiatives.
- Equal opportunities and inclusive employer, committed to providing a workplace free of discrimination and harassment.
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