Sr Clinical Research Associate Ii (Lead Monitor)

EY; Buenos Aires; Presencial; ARS 72.429.000 - 101.401.000; Jornada completa

Descripción de la vacante

A growing clinical research company is seeking a Sr Clinical Research Associate II (Lead Monitor) based in Buenos Aires. The candidate will facilitate regional projects, supervise study activities, and train monitors while ensuring compliance and quality monitoring. Proficiency in English and Spanish is essential, alongside a degree in Life Sciences or Pharmacy. This position provides a great opportunity to advance your career in clinical research with strong support and teamwork.

Formación

• Degree in a relevant field like Life Sciences or Pharmacy is required.
• Experience as a Lead/Senior Monitor in clinical projects.
• Ability to communicate with internal project teams and handle site budgets.

Responsabilidades

• Facilitate regional projects and supervise timelines and schedules.
• Train monitors and review monitoring reports.
• Act as main communication line between Monitor and Regional Lead.

Conocimientos

Independent on-site monitoring experience

Communication, leadership, and problem-solving skills

Full working proficiency in English and Spanish

Ability to plan, multitask and work in a dynamic team environment

PC skills with MS Word, Excel and PowerPoint

Educación

College/University degree in Life Sciences, Pharmacy, RN or equivalent

Descripción del empleo

Sr Clinical Research Associate Ii (Lead Monitor)

PSI CRO

Company DescriptionWe 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.If you feel it is time to make your skills and knowledge visible within a growing company with true focus on its people, then PSI is the right choice for you.

Job Description:Only CVs in English will be considered.

• Facilitate regional projects as Lead Monitor and supervise study activities, timelines and schedules
• Train Monitors in annotated monitoring visit reports
• Review monitoring reports and support monitors in their activities
• Act as the main communication line between Monitor and Regional Lead
• Facilitate site budgets and contract negotiations
• Be a point of contact for in-house support services and vendors
• Communicate with internal project teams regarding study progress and lead project team calls on the country level
• Participate in quality control and compliance monitoring
• May need to monitor and manage sites (if applicable)
• May need to supervise monitors on site
• Oversee and maintain study‑specific and corporate tracking systems at site and country level

• College/University degree in Life Sciences, Pharmacy, RN or an equivalent combination of education, training & experience
• Participation in clinical projects as a Lead/Senior Monitor
• Independent on‑site monitoring experience
• Full working proficiency in English and Spanish
• PC skills to be able to work with MS Word, Excel and PowerPoint
• Ability to plan, multitask and work in a dynamic team environment
• Communication, leadership, and problem‑solving skills
• Ability to travel

Additional InformationAdvance your career in clinical research, overseeing a variety of tasks and growing with the company. You will work closely with driven and dedicated cross‑functional teams, get all support and ownership of your projects.

Clinical Research Associate

PSI CRO

Company DescriptionWe 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...