En un coup d'œil
- Missions: Surveillez des études cliniques et maintenez les normes de qualité les plus élevées.
- Entreprise: PSI, une organisation de recherche contractuelle innovante avec 22 ans d'expérience.
- Avantages: Opportunités de développement professionnel, horaires flexibles et option de télétravail.
- Autres infos: Culture d'entreprise positive avec mentorat et formation approfondie.
- Pourquoi ce job: Développez vos compétences et devenez expert en recherche clinique dans un environnement dynamique.
- Qualifications: Diplôme en sciences de la vie et expérience en surveillance indépendante.
Le salaire estimé est compris entre 51750 - 63250 € par an.
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.
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)
- #J-18808-Ljbffr
Clinical Research Associate II employeur : PSI CRO
PSI est un employeur exceptionnel qui valorise la diversité et l'inclusion au sein de son équipe internationale de professionnels médicaux. En tant que membre de l'équipe de surveillance médicale, vous bénéficierez d'opportunités de croissance professionnelle tout en contribuant à des avancées significatives dans le domaine pharmaceutique. Avec un environnement de travail collaboratif et un engagement envers la sécurité des patients, PSI offre une carrière enrichissante au cœur de la science médicale.
