Remote Clinical Research Associate — Elevate Trials

IQVIA; United States; Remote; USD 35,000 - 73,000; Full time

Job summary

IQVIA is hiring Clinical Research Associates to perform monitoring and site management to ensure studies adhere to the protocol and all regulatory and sponsor requirements.

Responsibilities include site selection, initiation and monitoring visits, guiding recruitment planning, and maintaining essential study documentation. Candidates should have a Bachelor’s in a scientific field and at least 1 year of on-site trial monitoring experience.

Qualifications

• Bachelor's degree in a scientific or health-care field.
• At least 1 year experience on-site monitoring clinical trials.
• Knowledge of GCP and ICH guidelines.
• Proficiency with Word/Excel/PowerPoint and mobile devices.
• Written and verbal communication in Polish and English.
• Ability to establish effective working relationships with colleagues and clients.

Responsibilities

• Perform site selection, initiation, monitoring and close-out visits and maintain documentation.
• Support development of subject recruitment plans.
• Coordinate protocol training and ensure communication with sites.
• Evaluate site practices and escalate quality issues.
• Track regulatory submissions, recruitment, CRF completion and data queries.

Skills

Site monitoring

Site management

Regulatory knowledge (GCP/ICH)

Communication skills

MS Word/Excel/PowerPoint

Clinical trial documentation

Problem solving

Languages: Polish & English

Team collaboration

Data entry

Education

Bachelor's Degree in scientific discipline or health care

Tools

Microsoft Word

Microsoft Excel

PowerPoint

Job description

IQVIA is hiring Clinical Research Associates to perform monitoring and site management to ensure studies adhere to the protocol and all regulatory and sponsor requirements.

Responsibilities include site selection, initiation and monitoring visits, guiding recruitment planning, and maintaining essential study documentation. Candidates should have a Bachelor’s in a scientific field and at least 1 year of on-site trial monitoring experience.