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Salary
$24k – $60k per year (Estimated)
Location
Remote/Hybrid (Buenos Aires, Argentina)
Seniority
Senior · 2+ years exp
Employment
Full-Time
Overview
Company
Impact
Profile match

PSI

PSI (PSI CRO AG) is a privately owned, global full-service contract research organization (CRO) headquartered in Zug, Switzerland, with significant operational hubs across North and South America, Europe, Asia-Pacific, and the Middle East. Founded in 1995, PSI specializes in providing clinical trial management, monitoring, regulatory affairs, biostatistics, data management, and medical writing services for global pharmaceutical, biotechnology, and medical device companies.

We are the company that cares - for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2,500 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

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
  • 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

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.

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