Clinical Research Associate I

PSI CRO; Ciudad Autónoma de Buenos Aires; Híbrido; ARS 600.000 - 900.000; Jornada completa

Descripción de la vacante

A global Contract Research Organization is seeking a Clinical Research Associate (CRA) for a hybrid position in Buenos Aires, Argentina. In this role, you will be responsible for site monitoring, training staff, and managing study communications. Candidates should have a Bachelor's degree in Medicine and proficiency in both Spanish and English, with at least 2 years of relevant experience preferred. The position offers opportunities for career advancement and professional growth.

Servicios

Career development courses

Mentoring opportunities

Formación

• At least 2 years' experience in patient care and/or health care or clinical environment.
• Experience in Clinical Research is a plus.
• Availability to travel.

Responsabilidades

• Prepare and conduct monitoring visits.
• Deliver training to investigators and site staff.
• Perform CRF review and source document verification.
• Manage site communication.

Conocimientos

Communication skills

Collaboration skills

Problem-solving skills

Proficiency in MS Office

Full working proficiency in Spanish

Full working proficiency in English

Educación

Bachelor's degree in Medicine

Descripción del empleo

PSI is a leading Contract Research Organization with more than 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

Hybrid position in Buenos Aires. Only CVs in English will be considered.

We are looking for a CRA to join our team in Argentina. Here you will have the opportunity to develop yourself as a senior, trainer, mentor and leader. We are committed to developing our employees in their careers by providing tailored courses and mentoring.

Responsibilities will include:

• Preparation, conduct, and reporting of selection, initiation, routine and closeout monitoring visits
• Delivering training of investigators, site staff and project teams
• Work with complex studies
• Perform CRF review, source document verification and query resolution
• Be responsible for site communication and management
• Be involved in site identification process
• Contact for clinical investigators, vendors and support services in regard to study progress
• Participate in feasibility research
• Preparation and delivering of presentations at Investigator’s Meetings
• Preparation for and attendance at company’s audits; resolution of audit findings
• Support to Regulatory Affairs in procurement of site regulatory documents
• Maintenance of study-specific automated tracking systems

Qualifications

• Bachelor's degree in Medicine
• At least 2 years' experience in patient care and/or health care or clinical environment
• Full working proficiency in Spanish and English
• Experience in Clinical Research is a plus
• Availability to travel
• Proficiency in MS Office applications
• Ability to plan and work in a dynamic team environment
• Communication, collaboration, and problem-solving skills

Additional Information

Advance your career in clinical research, coordinating a variety of tasks and learning new things while growing with a rapidly growing company that puts its people first.