Senior CRA – Sponsor‑Dedicated (Italy)

IQVIA LLC; Milano; In loco; EUR 32.000 - 53.000; Tempo pieno

Vantaggi offerti da questo lavoro

Company car

Mobile phone

Benefits package

Descrizione del lavoro

IQVIA LLC is seeking an Experienced Clinical Research Associate for Italy. The role involves site selection, initiation, monitoring, and close-out visits, plus supporting recruitment planning and regulatory submissions to ensure GCP/ICH compliance.

The ideal candidate holds a Bachelor's and Master's in a scientific field, CRA certification, and strong English, with proven pharma or clinical trials experience. Travel flexibility and a valid B class driving license are required.

Competenze

• Bachelor's and Master's degrees in a scientific or healthcare field.
• CRA Certification required by ministerial decree dated 15.11.2011.
• Experience in pharma industry or clinical trials.
• Excellent command of English.
• Strong computer skills including MS Office.
• Excellent organizational and time management skills.
• Ability to establish and maintain effective working relationships.
• Flexibility to travel.
• Driver’s license class B.

Mansioni

• Performing site selection, initiation, monitoring and close-out visits
• Supporting the development of a subject recruitment plan
• Evaluating the quality and integrity of site practices in accordance with regulatory requirements (GCP/ICH)
• Managing progress by tracking regulatory submissions, recruitment, CRF completion and data queries
• Collaborating with study sites and client representatives

Conoscenze

English proficiency

Organizational skills

Time management

Problem-solving

Interpersonal skills

Travel flexibility

Driving license

Formazione

Bachelor's Degree in scientific discipline or health care

Master's Degree in scientific discipline or health care

CRA Certification (Ministerial Decree 15.11.2011)

Strumenti

MS Office

Descrizione del lavoro

IQVIA LLC is seeking an Experienced Clinical Research Associate for Italy. The role involves site selection, initiation, monitoring, and close-out visits, plus supporting recruitment planning and regulatory submissions to ensure GCP/ICH compliance.

The ideal candidate holds a Bachelor's and Master's in a scientific field, CRA certification, and strong English, with proven pharma or clinical trials experience. Travel flexibility and a valid B class driving license are required.