CRA2 - Santiago de Chile

Santiagoonsite

Posted today · via Workday

About this role

Job Overview: The Clinical Research Associate 2 (CRA 2) is responsible for monitoring and managing clinical trial sites to ensure adherence to study protocols regulatory requirements and guidelines. The CRA plays a key role in site management subject recruitment and data quality while maintaining clear communication with study teams and stakeholders. Responsibilities: Conduct site monitoring visits including selection initiation monitoring and close-out visits in compliance with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Work with sites to adapt drive and track subject recruitment plans in alignment with project needs to enhance predictability.…

Read the full description on IQVIA RDS's site →

What we'd score you on

reqspace match rubric

Five dimensions, recruiter-grade. Upload your resume and we'll generate a written explanation of where you fit and where the gaps are.

1

Skills match

For this role: gcp, teams

2

Level fit

We check your title trajectory against the seniority signal of the role.

3

Domain experience

Your work in the role's domain matters more than your years total. We weight recent and direct experience.

4

Recency

A skill you used last quarter weighs more than one from five years ago. We grade on recency, not lifetime.

5

Location fit

This role is based in Santiago. We weight your proximity and willingness to relocate.

Score yourself on this role.
Free · no card · written explanation included
See if I'm a fit →

Skills in this role

Pulled from the job description. These are the keywords we'll weight when scoring your fit.

gcpteams

More at IQVIA RDS

See all open jobs at IQVIA RDS