About The Position
As a Clinical Research Associate at PSI, you will perform a variety of monitoring tasks and work on clinical studies across different therapeutic indications while maintaining high quality standards. The role includes onsite monitoring, study startup and feasibility research, review of clinical documentation, site management and communication, and collaboration with internal project teams, support services, vendors, and regulatory staff. The position offers an opportunity to develop skills, broaden therapeutic area experience, and build expertise in clinical research.
Requirements
- College or university degree in Life Sciences, or an equivalent combination of education, training, and experience.
- Independent onsite monitoring experience in Argentina.
- Experience conducting all types of monitoring visits in Phase II and Phase III studies.
- Full working proficiency in English and Spanish.
- Proficiency in MS Office applications.
- Ability to plan and work in a dynamic team environment.
- Communication, collaboration, and problem-solving skills.
- Ability to travel.
Nice To Haves
- Experience in Oncology.
Responsibilities
- Conduct and report all types of onsite monitoring visits.
- Participate in study startup and feasibility research.
- Perform CRF review, source document verification, and query resolution.
- Manage sites and communicate with site personnel.
- Serve as a point of contact for in-house support services and vendors.
- Communicate study progress to internal project teams.
- Support the regulatory team in preparing documents for study submissions.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
