Clinical Research Associate.

PSI; Buenos Aires; Presencial; ARS 60.635.000 - 106.112.000; Jornada completa

Descripción de la vacante

PSI in Argentina is seeking a Clinical Research Associate (CRA) to join our expanding team. You will have the opportunity to develop as a senior professional, trainer, mentor, and leader, with tailored courses and mentoring to advance your career.

Responsibilities include monitoring visits, training site staff, working with complex studies, CRF review, and audits. You will engage in feasibility research and contribute to Investigator Meetings while coordinating with investigators and vendors

Formación

• 2+ years experience in patient care and/or health care or clinical environment.
• Proficiency in MS Office applications.
• Full working proficiency in Spanish and English.
• Experience in Clinical Research.

Responsabilidades

• Preparation, conduct, and reporting of monitoring visits and closeout visits.
• Deliver training of investigators, site staff and project teams.
• Work with complex studies and CRF review, source document verification and query resolution.
• Site communication and management; involvement in site identification processes.
• Liaise with investigators, vendors and support services regarding study progress.
• Participation in feasibility research and Investigator Meetings.

Conocimientos

Bilingual Spanish/English

MS Office

Communication skills

Teamwork

Problem solving

Educación

Life Sciences degree

Herramientas

MS Office

Descripción del empleo

Job Description

Only CV's 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 develop 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

• College/University Degree in Life Sciences;


• 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


• 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 rapid growing company that puts its people first.