Clinical Research Associate: Site Monitoring & Coordination

IQVIA; Fort Lauderdale (FL); On-site; USD 75,000 - 198,000; Full time

Job summary

IQVIA is seeking a Clinical Research Associate to monitor sites and ensure adherence to the study protocol, regulatory requirements, and sponsor expectations. You will conduct site visits, administer training, and manage communications with site personnel.

The role requires prior on-site monitoring experience, strong regulatory knowledge, and excellent English communication. Proficiency with EDC/CTMS/eTMF is preferred, with potential travel to sites as needed.

Qualifications

• Requires at least 2 years of independent on-site monitoring experience as a Clinical Research Associate (CRA).
• Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (GCP/ICH).
• Excellent written and verbal communication skills in English.

Responsibilities

• Perform site monitoring visits (selection, initiation, monitoring and close-out) per scope of work and GCP.
• Drive subject recruitment plan with sites to enhance predictability according to project needs.
• Administer protocol training to sites and establish regular communication lines.

Skills

On-site monitoring

Regulatory knowledge

Communication skills

Time management

Problem solving

Education

Bachelor's Degree in scientific discipline or health care

Tools

EDC

CTMS

eTMF

IVRS/IWRS

Job description

IQVIA is seeking a Clinical Research Associate to monitor sites and ensure adherence to the study protocol, regulatory requirements, and sponsor expectations. You will conduct site visits, administer training, and manage communications with site personnel.

The role requires prior on-site monitoring experience, strong regulatory knowledge, and excellent English communication. Proficiency with EDC/CTMS/eTMF is preferred, with potential travel to sites as needed.