Experienced Clinical Research Associate - Multi-Sponsored Model

IQVIA; United States; Remote; USD 65,000 - 90,000; Full time

Job summary

IQVIA is seeking a Clinical Research Associate (CRA) to support site visits and monitoring activities from a home-based role in the United States. You will receive structured mentoring and quarterly reviews to progress in your career path.

Typical responsibilities include site visits, recruitment planning, and training delivery while ensuring quality and regulatory compliance. Frequent travel to sites is expected, and fluency in English and Arabic is required.

Qualifications

• Bachelor’s degree in health care or related scientific field.
• 1.5–2 years of on-site monitoring experience.
• Fluent in Arabic and English.
• Good written and verbal English communication skills.
• Requires frequent travel to sites.
• Home-based with travel connectivity.
• Knowledge of clinical research regulatory requirements is a plus.

Responsibilities

• Perform site selection, initiation, monitoring and close-out visits with proper documentation.
• Assist in developing a subject recruitment plan.
• Establish regular communication and provide protocol and study training to sites.
• Evaluate quality and integrity of site practices and escalate issues as needed.
• Track regulatory submissions, recruitment, CRF completion and data query resolution.

Skills

On-site monitoring

Regulatory submissions

Site coordination

Arabic language

English language

Education

Bachelor's degree in health care or scientific discipline

Job description

If you want to do your next step as a CRA, this is your chance!

You’ll have training and development to plan and progress your career in the direction you choose. And you won’t do it alone – you will have dedicated mentoring and receive structured quarterly reviews on performance, promotion and bonus awards.

While Projects Vary, Your Typical Responsibilities Might Include

• Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation
• Supporting the development of a subject recruitment plan
• Establishing regular lines of communication plus administering protocol and related study training to assigned sites
• Evaluating the quality and integrity of site practices – escalating quality issues as appropriate
• Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution

You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements.

You Should Have

• A Bachelor’s degree in a health care or other scientific discipline or educational equivalent
• At least 1,5 - 2 years of on-site monitoring experience
• Fluent in Arabic and English language
• Good written and verbal communication skills including good command of English language
• Requires frequent travel to sites
• Flexible about location, but location must have good connectivity to travel
• Homebased

If you want to make an impact in the global research market, where we are working to make a real difference in patient health, we ask you to

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.