Clinical Research Associate

Duties and Responsibilities of a CRA (Senior Monitor) are:

• Take ownership of assigned studies
• Carry out site selection and feasibility
• To act as the main point of communication with Investigator and the team
• When requested to support preparation of regulatory and / or EC submission
• Participate in mentoring/training of new staff as well as performing co-monitoring visits, to assess junior staff performance
• On-Site Monitoring
• Performing close out visits
• Reference: 9Ibw0NbXwDCyoRt7nCClxEjmaTCqH_q1AMXhIpE7uH5cFl0SwdR8cS5xYi5UhqNV

Qualification

• College/University degree in Life Sciences or an equivalent combination of education, training & experience
• 2 years on-site monitoring experience in phase 2/3 trials, ideally with experience of complex trials
• Full working proficiency in English
• Ability to plan, multitask and work in a dynamic team environment
• Communication, collaboration, and problem-solving skills
• Ability to travel