Clinical Research Associate II (Contract based)

PSI is a leading Contract Research Organization with more than 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees.  We focus on delivering quality and on-time services across a variety of therapeutic indications. As a Contract Clinical Research Associate II, you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications.  You will build and maintain relationships with clinical sites and investigators. You will focus on subjects’ rights, safety and well-being and quality of data compliance. Home-based (freelance) You will: - Conduct and report all types of onsite monitoring visits - Be involved in study startup  - Perform CRF review, source document verification and query resolution - Be responsible for site communication and management - Supervise study activities, timelines, and schedules on the country level - Be a point of contact for in-house support services and vendors - Be involved in quality control, such as compliance monitoring and reports review - Participate in feasibility research - Support regulatory team in preparing documents for study submissions - College/University degree in Life Sciences or an equivalent combination of education, training & experience - A minimum of 1 year of independent on-site monitoring experience in Portugal - Experience in all types of monitoring visits in Phase II and/or III - Experience in IBD/Inflammatory Bowel Diseases is mandatory - Full working proficiency in English and Portuguese  - Proficiency in MS Office applications - Ability to plan, multitask and work in a dynamic team environment - Communication, collaboration, and problem-solving skills - Ability to travel Make the right call and take your career to a whole new level.  Join the company that focuses on its people and invests in their professional development and success.