Fortrea

Global CRO providing Phase I-IV trials

Clinical Research Associate

Clinical Research OperationsConfirmed live in the last 24 hours

Full-timeNo salary listed

About the Job

Requirements

A university or college degree in life sciences, nursing, pharmacy, or a related allied health profession is required; equivalent relevant experience may be considered in place of formal education.
Basic to good knowledge of International Council for Harmonisation Good Clinical Practice (ICH/GCP) guidelines and applicable local laws and regulations governing clinical trials.
A solid understanding of clinical research processes, regulations, and methodology is required.
Strong organizational and time-management skills are required.
Ability to build and maintain relationships is required.
One to three years of monitoring experience within a contract research organization (CRO) or pharmaceutical environment is required.

Responsibilities

Identify and assess potential investigators and sites.
Recommend sites during feasibility and selection phases.
Conduct pre-study, initiation, monitoring, and close-out visits.
Monitor site performance, data quality, and protocol compliance.
Serve as a key point of contact for site personnel, providing training and support.
Use data insights to assess risks and drive decisions.
Support regulatory audits, ethics committee (EC) submissions, and system access coordination.
Monitor sites in Austria and Switzerland.

Make a meaningful impact in clinical research by joining our sponsor-dedicated team as a Clinical Research Associate (CRA). This role offers the opportunity to monitor sites in Austria and in Switzerland, while working on cutting-edge studies that shape the future of healthcare.

Key Responsibilities:

Identify and assess new potential investigators and sites.
Recommend sites during feasibility and selection phases.
Conduct pre-study, initiation, monitoring, and close-out visits.
Monitor site performance, data quality, and protocol compliance.
Act as a key point of contact for site personnel, providing training and support.
Use data insights to assess risks and drive decisions.
Support regulatory audits, EC submissions, and system access coordination.

Required Qualifications :

University or college degree in life sciences, nursing, pharmacy, or a related allied health profession; equivalent relevant experience may be considered in lieu of formal education.
Basic to good knowledge of ICH/GCP Guidelines and applicable local laws and regulations governing clinical trials.
Solid understanding of clinical research processes, regulations, and methodology.
Strong organizational and time management skills.
Ability to build and maintain relationships
1 to 3 years of monitoring experience required within CRO or Pharma environment.

Why Join Us?

Be part of a sponsor-dedicated team with a strong pipeline and purpose.
Enjoy regional monitoring—minimizing travel while maximizing your impact.
Collaborate with passionate professionals in a supportive environment.
Contribute to meaningful research that improves lives.

We invite qualified candidates who are committed to excellence in clinical research to apply and become part of Fortrea’s mission to advance healthcare worldwide. If you are seeking a rewarding opportunity within a globally respected organization, we encourage you to submit your application today.

#LI-GQ1 #LI-Remote

Learn more about our EEO & Accommodations request here.

About the Company

Fortrea

Global CRO providing Phase I-IV trials

Fortrea is a global contract research organization that provides clinical development services for the life sciences industry. It offers full service, functional service, and hybrid outsourcing models across Phase I–IV trials, clinical pharmacology, and consulting, serving biotech, biopharma, medical devices, and diagnostics. Its work is delivered through a network of investigators and specialized teams in approximately 100 countries, supporting trial design, execution, data management, and regulatory compliance. Fortrea’s approach combines its legacy experience from Covance and Labcorp with a pureplay CRO model to deliver fit-for-purpose solutions and agile project delivery. This positions it to manage trials across more than 20 therapeutic areas with scientific rigor and operational excellence. The company aims to bring predictability to clinical trial execution and help clients turn research ideas into real-world outcomes.

Company size: 10,001+
Company stage: IPO
Headquarters: Winston-Salem, NC
Founded: 2023

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