Company Description

PSI is a leading Contract Research Organization with more than 29 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 visitsPerform CRF review, source document verification and query resolutionBe responsible for site communication and managementBe a point of contact for in-house support services and vendorsCommunicate with internal project teams regarding study progressParticipate in feasibility researchSupport regulatory team in preparing documents for study submissionsPrepare and participate on audits and inspections

QualificationsCollege/University Life Sciences Degree and a Master´s Degree in Clinical Trials is required.At least 1 year of independent on-site monitoring experience in SpainExperience in all types of monitoring visits in Phase II and/or IIIFull working proficiency in English, Spanish and CatalanProficiency in MS Office applicationsAbility to plan, multitask and work in a dynamic team environmentCommunication, collaboration, and problem-solving skillsAbility to travel

 

Additional Information

What We Offer:

Stability, long-term cooperationPermanent contract, full-time jobCompetitive salary and benefit packageCareer development Unique combination of team collaboration and independent workFriendly and supportive colleaguesOnboarding courses about clinical research industryComfortable and well established office

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