Remote Lead Gen & Talent Outreach — Entry Level

Tecpetrol; Quilmes; Remote; ARS 600,000 - 1,000,000; Full time

Job summary

ThermoFisher Scientific in Buenos Aires is hiring an Entry Level Clinical Research Associate I to support monitoring and site management activities. You will coordinate monitoring tasks, conduct on-site or remote visits to ensure protocol adherence and regulatory filing, and help manage sponsor-driven procedures (FSO, FSP).

The role is ideal for individuals starting a career in clinical research, offering exposure to global trials and diverse regulatory environments in a corporate setting.

Qualifications

• Entry-level Clinical Research Associate role within a global CRO environment.
• Position supports study coordinators, aCRA, and CTAs in clinical trials.
• Role involves coordination of monitoring activities and regulatory tasks.

Responsibilities

• Coordinate various aspects of clinical monitoring and site management.
• Conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation.
• Manage procedures and guidelines from different sponsors and monitoring environments (FSO, FSP).

Skills

Clinical monitoring

Regulatory compliance

Documentation management

Job description

FSP CRA I (Entry Level) - open for Study Coordinators, aCRA and CTAs

Buenos Aires ThermoFisher Scientific

**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
Join Us as a Clinical Research Associate I - Make an Impact at the Forefront of Innovation
We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.
As part of our global team, you'll have the opportunity to perform and coordinate different aspects of the clinical monitoring and site management process. As a Clinical Research Associate I, you'll conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation. You will manage procedures and guidelines from different sponsors and/or monitoring environments (i.e., FSO, FSP