Clinical Research Associate: Site Monitoring & Execution

IQVIA; New York (NY); On-site; USD 75,000 - 198,000; Full time

Job summary

IQVIA is seeking a Clinical Research Associate (CRA) to monitor study sites in accordance with the protocol, GCP, and sponsor requirements. You will perform site visits, manage recruitment tracking, and ensure data quality and regulatory compliance across assigned studies.

The role requires on-site monitoring experience, strong communication, and proficiency with EDC/CTMS/eTMF systems, along with English-language proficiency.

Qualifications

• Bachelor's degree in scientific discipline or health care preferred.
• At least 2 years of on-site monitoring experience as a Clinical Research Associate (CRA).
• Equivalent combination of education, training and experience may be accepted in lieu of degree.
• Good knowledge of applicable clinical research regulatory requirements (GCP/ICH).
• Proficiency in Microsoft Word, Excel, and PowerPoint; comfortable with laptop, iPhone and iPad where applicable.
• Experience using EDC, CTMS, eTMF, IVRS/IWRS to support monitoring activities.
• Excellent written and verbal English communication skills.
• Strong organizational and problem-solving abilities.
• Ability to establish effective working relationships with coworkers, managers, and clients.

Responsibilities

• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) per scope of work and GCP.
• Drive and track subject recruitment plans to enhance study predictability.
• Administer protocol and study training to sites and maintain regular site communication.

Skills

Attention to detail

Time management

Communication skills

English proficiency

Team collaboration

Regulatory knowledge

Education

Bachelor's degree in scientific discipline or health care

Tools

EDC

CTMS

eTMF

IVRS/IWRS

MS Word

MS Excel

PowerPoint

Job description

IQVIA is seeking a Clinical Research Associate (CRA) to monitor study sites in accordance with the protocol, GCP, and sponsor requirements. You will perform site visits, manage recruitment tracking, and ensure data quality and regulatory compliance across assigned studies.

The role requires on-site monitoring experience, strong communication, and proficiency with EDC/CTMS/eTMF systems, along with English-language proficiency.