[Hiring] CRA II @PSI CRO

Role Description

As a Contract CRA 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

Qualifications

• 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

Benefits

• 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.