Job Overview
The Clinical Research Associate role involves ensuring the rights and well-being of trial participants are safeguarded, and reported data are accurate, complete, and verifiable from source documents.
Key Responsibilities
* BUILD RELATIONSHIPS WITH PRINCIPAL INVESTIGATORS, STUDY COORDINATORS, PHARMACISTS, AND ALL RELEVANT SITE TRIAL PERSONNEL TO ENSURE EFFICIENT MANAGEMENT OF CLINICAL TRIALS.
* Foster customer relationships to deliver projects efficiently, timely, and productively as per study requirements and timelines.
* Collaborate with internal teams, prepare site essential documents, and support ethics and regulatory submission processes.
* Recruit participants as per site targets, drive site recruitment initiatives, and prepare site-specific plans.
* Monitor investigational sites according to ICH GCP guidelines.
Requirements
* Graduate in a clinical or life sciences-related field.
* Relevant experience/qualifications may also be considered.
* Minimum 6 months of CRA independent monitoring experience.
* 2+ years of CRA independent monitoring experience.
What We Offer
We offer flexible working arrangements and work-life balance to ensure our staff achieve their goals.
We are committed to providing an inclusive work environment where everyone is treated fairly and with respect.