Clinical Research Associate II

As a Clinical Research Associate II at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry.

You will:

Conduct and report all types of onsite monitoring visits

Be involved in study startup (if applicable)

Perform CRF review, source document verification and query resolution

Be responsible for site communication and management

Be a point of contact for in-house support services and vendors

Communicate with internal project teams regarding study progress

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

Independent on-site monitoring experience in North America.

Experience in all types of monitoring visits in Phase II and/or III

Full working proficiency in English and French.

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

Valid driver’s license

This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.

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.

Originally posted on Himalayas