Clinical Research Associate II at PSI CRO

Saint-Maur-des-Fossés, Ile-de-France, France -

Full Time

Start Date

Immediate

Expiry Date

08 Sep, 26

Salary

0.0

Posted On

10 Jun, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

On-site Monitoring, CRF Review, Source Document Verification, Query Resolution, Site Management, Study Startup, Feasibility Research, Regulatory Documentation, Oncology, Hemophilia, Infectious Diseases, Gastrointestinal, English Proficiency, MS Office, Multitasking, Problem-solving

Industry

Pharmaceutical Manufacturing

Description

Company Description PSI is a leading Contract Research Organization with more than 22 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 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 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 Qualifications College/University degree in Life Sciences or an equivalent combination of education, training & experience Independent on-site monitoring experience in France Experience in all types of monitoring visits in Phase II and/or III Experience in oncology, hemophilia, infectious diseases, GI Full working proficiency in English 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 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. We offer: Big professional advancement opportunity within Clinical Operations with specific mentorship and training program Development opportunities across PSI departments Flexible working hours Home-office option available, as well as combination of home and office work arrangement Extensive onboarding trainings and professional development training programs Highly developed company culture and positive team atmosphere Additional leave days (12 days of RTT)

Responsibilities

The role involves conducting and reporting all types of onsite monitoring visits and managing site communications. Responsibilities include CRF review, source document verification, and supporting the regulatory team with study submissions.