Lead Clinical Research Associate

PSI is a leading Contract Research Organization with more than 30 years in the industry. The company offers a perfect balance between stability and innovation to both clients and employees. The Lead Clinical Research Associate coordinates investigator/site feasibility and identification process, as well as study startup, monitors project timelines and patient enrollment, and ensures reporting compliance. The role also involves managing Monitors, coordinating safety information flow, and performing clinical supplies management with vendors.

Requirements

• Relevant educational background, such as MD, MPharm, RN or College/University degree in Life Sciences or an equivalent combination of education, training and experience.
• Minimum of 4 years’ site monitoring experience with participation in global clinical projects as a Lead Monitor or equivalent qualification level.
• Must have prior experience monitoring or managing sites and CRAs in the United States with knowledge of US regulatory guidelines and practices.
• Full working proficiency in English.
• Proficiency in MS Office applications.
• Ability to plan, multitask and work in a dynamic team environment.
• Excellent Communication, collaboration, and problem-solving skills.
• Ability to travel up to 65% (depending on project needs).
• Valid driver’s license (if applicable).