Senior Clinical Research Associate: Trials & Remote

IQVIA; United States; Remote; USD 45,000 - 98,000; Full time

Benefits offered by this job

Home-office

Company car

Job summary

IQVIA is seeking a sponsor-dedicated Senior CRA in Poland to work with leading pharma clients and gain diverse therapeutic experience. You’ll receive world-class training, mentoring, and opportunities for professional growth within a global CRO.

The role emphasizes on-site monitoring, regulatory compliance, and collaboration with study sites and client teams, with travel as needed. IQVIA offers career development and a dynamic work environment.

Qualifications

• 3 years minimum on-site monitoring experience.
• GCP/ICH regulatory knowledge.
• Excellent written and verbal communication.
• Fluent Polish and English.
• Willingness to travel.

Responsibilities

• Perform site selection, initiation, monitoring and close-out visits.
• Support development of subject recruitment plan.
• Evaluate site practice quality per GCP/ICH.
• Track regulatory submissions, recruitment, CRF completion, data queries.
• Collaborate with study site and client representatives.
• Depending on client model, remote-monitoring or start-up involvement.

Skills

On-site monitoring

GCP/ICH knowledge

Strong communication

Polish & English

Education

Life science degree or healthcare apprenticeship

Job description

IQVIA is seeking a sponsor-dedicated Senior CRA in Poland to work with leading pharma clients and gain diverse therapeutic experience. You’ll receive world-class training, mentoring, and opportunities for professional growth within a global CRO.

The role emphasizes on-site monitoring, regulatory compliance, and collaboration with study sites and client teams, with travel as needed. IQVIA offers career development and a dynamic work environment.