Senior CRA - Sponsor-Dedicated, Remote Belgium

IQVIA; Zaventem; Presencial; EUR 60 000 - 85 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Company car

Mobile phone

Rewards & benefits package

Resumo da oferta

IQVIA Belgium seeks a Senior Clinical Research Associate to join our Sponsor dedicated model, home‑based in Belgium. You will perform site monitoring per GCP/ICH, support recruitment plans, train sites, maintain TMF/ISF accuracy, and collaborate with cross‑functional teams.

A strong, multilingual CRA with 3+ years on‑site monitoring is preferred. We offer development, onboarding, and opportunities within a global organization.

Qualificações

• University degree in scientific discipline or health care.
• Minimum of 3 years of independent on-site monitoring experience as a CRA within a CRO or pharmaceutical environment.
• Excellent communication skills in Dutch, French, and English, both written and spoken.
• Good knowledge of applicable clinical research regulatory requirements (GCP and ICH).
• Organizational and problem-solving skills.
• Interpersonal and cross-cultural communication skills to build strong partnerships with Belgium site investigators.

Responsabilidades

• Perform site monitoring visits (selection, initiation, monitoring and close-out) per contracted scope and regulatory requirements (GCP/ICH).
• Work with sites to drive and track subject recruitment plan.
• Administer protocol training to sites and maintain regular communication.
• Evaluate site practices for protocol conduct and regulatory adherence.
• Escalate quality issues as appropriate.
• Manage progress by tracking submissions, recruitment, CRF completion and data queries.
• May support start-up and TMF/ISF filings.
• Collaborate with study team for project execution.

Conhecimentos

Multilingual: Dutch, French, English

GCP/ICH knowledge

Organizational skills

Problem solving

Formação académica

University degree in scientific discipline or health care

Descrição da oferta de emprego

IQVIA Belgium seeks a Senior Clinical Research Associate to join our Sponsor dedicated model, home‑based in Belgium. You will perform site monitoring per GCP/ICH, support recruitment plans, train sites, maintain TMF/ISF accuracy, and collaborate with cross‑functional teams.

A strong, multilingual CRA with 3+ years on‑site monitoring is preferred. We offer development, onboarding, and opportunities within a global organization.