Senior Oncology CRA: Site Partnerships & Compliance

AbbVie; Roma; In loco; EUR 60.000 - 90.000; Tempo pieno

Vantaggi offerti da questo lavoro

Life insurance

Medical plan

Flexible benefits

Company car

Descrizione del lavoro

AbbVie is seeking a clinical research professional to advance our pipeline by partnering with study teams, internal R&D, investigators, and site staff. You will ensure compliant conduct, data integrity, and strong customer experience across clinical trials.

You will mentor CRAs, drive site engagement strategies, and contribute to risk assessment and mitigation to uphold study quality and patient safety in a dynamic environment.

Competenze

• Bachelor’s degree or equivalent; health related preferred.
• Valid driver’s license.
• Minimum of 1 year of clinically related experience, of which 6 months in clinical research monitoring.
• Knowledge of therapeutic area indications with ability to apply scientific concepts.
• Advanced knowledge of local regulatory and ICH/GCP guidelines.
• Strong cross-functional collaboration skills.
• Strong planning and organizational skills.
• Advanced ability to leverage technology for site support.
• Strong interpersonal, written and presentation skills.
• Integrity and fast-paced delivery.

Mansioni

• Primary Sponsor point of contact for the investigative site.
• Aligns, trains and motivates site staff and principal investigator on trial goals and patient treatment principles.
• Conducts site evaluation, training, monitoring, and site closure activities with compliance to procedures and regulations.
• Develops site engagement strategy and reports progress and impact.
• Mentors and trains less experienced CRAs.
• Participates in global/local task forces and initiatives as assigned.
• Proactively manages site risk and coordinates with Central Monitoring for risk mitigation.
• Identifies potential investigators/sites to support planned studies.
• Ensures data quality and timely safety reporting by site personnel.
• Maintains audit readiness at assigned sites.
• Manages investigator payments as per contracts.

Conoscenze

Clinical research monitoring

GCP & ICH guidelines

Site engagement

Regulatory knowledge

Cross-functional collaboration

Mentoring CRAs

Risk assessment

Data quality focus

Formazione

Bachelor's degree or equivalent

Health-related preferred

Descrizione del lavoro

AbbVie is seeking a clinical research professional to advance our pipeline by partnering with study teams, internal R&D, investigators, and site staff. You will ensure compliant conduct, data integrity, and strong customer experience across clinical trials.

You will mentor CRAs, drive site engagement strategies, and contribute to risk assessment and mitigation to uphold study quality and patient safety in a dynamic environment.