Clinical Research Associate (CRA)

Responsibilities

Leverage your expertise. Conduct qualification visits (QV), site initiation visits (SIV), monitoring visits (MV) and termination visits (TV) at assigned clinical sites and generate visit/contact reports

Build relationships. Oversee integrity of the study and utilize problem-solving skills to promote rapport with the site and staff

Protect patients. Review the performance of the trial at designated sites, ensure the rights and well-being of human subjects are safeguarded and are in accordance with protocol

Drive productivity. Develop patient recruitment strategies in conjunction with the clinical site to meet enrollment timelines while also Ensuring compliance with the approved standard operating procedures (SOPs), protocol/amendment(s), GCP, and the applicable regulatory requirement(s)

Ensure quality. Evaluate the quality and integrity of the reported data, site efficacy and drug accountability

Execute. Monitor completeness and quality of Regulatory Documentation and perform site document verification

Benefits

Remote work

World-class technology and training catered to your individual experience

Less travel and a lower protocol load in comparison to industry peers

Bonus incentive program

Opportunity to work within multiple therapeutic areas

Opportunity to advance your career in clinical research

Regular clinical research team discussions in an open environment to share expertise and promote learning

Management support and encouragement for career growth through consistent performance discussions and evaluations

Career opportunities to progress into a more senior CRA role, line management, Quality, Project Leadership, or other positions

Glassdoor

3.8

Global clinical research and biopharmaceutical services company.

Raleigh, North Carolina, USA

http://www.parexel.com

Distribution of Different Job Fields Receiving Sponsorship

Represents job field similar to this job

Education and Training

Engineering and Development

Management and Executive

Accounting and Finance

Legal and Compliance

Customer Service and Support

Sales

Marketing

Human Resources

Trends of Total Sponsorships

*2026

(38)

2025

(31)

Qualifications

18+ months of direct onsite monitoring experience as a Clinical Research Associate (CRA)

Bachelors or equivalent degree in biological science, pharmacy or other health related discipline

Strong interpersonal, written, and verbal communication skills within a matrixed team

Ability to work in a self-driven capacity with a sense of urgency and limited need for oversight

A client focused approach to work with a flexible attitude with respect to assignments and new learning

The ability to manage multiple tasks, evaluate a variety of unpredictable scenarios and achieve project timelines while being able to apply your understanding of study protocol(s)

An honest and ethical work approach to promote the development of life changing treatments for patients

Strong computer skills, including but not limited to the knowledge of a Clinical Trial Management System (CTMS), Electronic Document Management System (EDMS) and MS-Office products such as Excel and Word

Required skills

Clinical Site Monitoring, Clinical Study Protocols, Microsoft Excel, Microsoft Word

Experience

1+ years