Clinical Research Associate: Sponsor-Dedicated Monitoring

IQVIA; Camden (NJ); On-site; USD 72,000 - 189,000; Full time

Job summary

IQVIA is seeking an on-site Clinical Research Monitor in New Jersey to ensure sites conduct studies per protocol and regulatory requirements. You will monitor visits, support recruitment plans, and train site staff, maintaining clear communication and documentation.

The role requires at least 2 years of on-site monitoring experience, knowledge of GCP/ICH, and strong organizational and communication skills. This is an on-site position in the US with potential collaboration across teams.

Qualifications

• Bachelor’s Degree in scientific discipline or health care preferred.
• Requires at least 2 years of on-site monitoring experience.
• Equivalent combination of education, training and experience may be accepted in lieu of degree.
• Good knowledge of, and skill in applying, applicable clinical research regulatory requirements.

Responsibilities

• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
• Work with sites to adapt, drive, and track subject recruitment plan to enhance predictability.
• Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
• Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations.
• Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, CRF completion and submission, and data query generation and resolution.

Skills

English proficiency

Communication skills

Time management

Organizational skills

Education

Bachelor's degree in scientific discipline or health care

Equivalent combination of education, training and experience

Tools

Microsoft Word

Excel

PowerPoint

iPhone/iPad usage

Job description

IQVIA is seeking an on-site Clinical Research Monitor in New Jersey to ensure sites conduct studies per protocol and regulatory requirements. You will monitor visits, support recruitment plans, and train site staff, maintaining clear communication and documentation.

The role requires at least 2 years of on-site monitoring experience, knowledge of GCP/ICH, and strong organizational and communication skills. This is an on-site position in the US with potential collaboration across teams.