Senior Clinical Research Associate

Job description

Company Description PSI is a leading Contract Research Organization with 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.

Job Description As a Clinical Research Associate 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 SIV, RMV, COV onsite monitoring visits

- 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

- Prepare and particiapte on audits and inspections

Qualifications

- College/University degree in Life Sciences or an equivalent combination of education, training & experience

- Independent on-site monitoring experience

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

- Experience in Oncology is a plus

- Full working proficiency in English and French is essential.

- 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

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