Clinical Research Associate II — On-Site Monitoring Pro

IQVIA Inc; Durham (NC); In loco; USD 75.000 - 198.000; Tempo pieno

Descrizione del lavoro

IQVIA is seeking a Clinical Research Associate II with independent on-site monitoring experience to join our team in the United States. You will conduct site selection, initiation, routine monitoring, and closeout visits in accordance with GCP, ICH, and applicable regulatory requirements while training site staff.

You will build strong investigator relationships, monitor progress, ensure TMF readiness, prepare monitoring reports, and collaborate with cross-functional teams to support patient

Competenze

• Bachelor's degree required.
• Minimum 1 year of independent on-site monitoring experience in a CRO, biotech or pharmaceutical.
• Working knowledge of GCP, ICH, and clinical trial regulations.
• Strong communication, organizational, and problem-solving skills.
• Proficiency with Microsoft Office applications.

Mansioni

• Conduct site selection, initiation, routine monitoring, and closeout visits.
• Prepare monitoring reports, follow-up communications, and TMF documentation.
• Collaborate with cross-functional study teams to support project delivery and milestones.
• Support patient recruitment and retention initiatives at the site level.
• Assist with site financial and administrative activities, including invoice management.

Conoscenze

GCP knowledge

ICH guidelines

Communication skills

Organizational skills

Problem-solving skills

MS Office proficiency

Formazione

Bachelor's degree

Strumenti

Microsoft Office

Descrizione del lavoro

IQVIA is seeking a Clinical Research Associate II with independent on-site monitoring experience to join our team in the United States. You will conduct site selection, initiation, routine monitoring, and closeout visits in accordance with GCP, ICH, and applicable regulatory requirements while training site staff.

You will build strong investigator relationships, monitor progress, ensure TMF readiness, prepare monitoring reports, and collaborate with cross-functional teams to support patient