Clinical Research Associate, Sponsor Dedicated - Italy

IQVIA; Milano; In loco; EUR 40.000 - 60.000; Tempo pieno

Descrizione del lavoro

A leading global clinical research company seeks an experienced Clinical Research Associate in Milan. You will perform site visits, support recruitment strategies, and ensure compliance with regulatory standards. Ideal candidates hold a Bachelor's and Master's in a relevant field and possess excellent English skills. This role offers career growth with benefits, including a company car and flexible work schedules.

Servizi

Company car

Mobile phone

Attractive benefits package

Competenze

• Experience in Pharma Industry and/or Clinical Trials environment.
• Ability to establish and maintain effective working relationships.
• Driver’s license class B required.

Mansioni

• Perform site selection, initiation, monitoring, and close-out visits.
• Support the development of a subject recruitment plan.
• Evaluate quality and integrity of site practices.

Conoscenze

Organizational skills

Time management

Problem-solving skills

Flexibility to travel

Excellent command of English

Formazione

University Bachelor's Degree in a scientific discipline or healthcare

Master's Degree in a scientific discipline or healthcare

CRA Certification

Descrizione del lavoro

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Clinical Research Associate, Sponsor Dedicated - Italy, Milan

Client: IQVIA

Location: Milan, Italy

Job Category: Other

EU work permit required: Yes

Job Reference: 84bab8f5f99c

Job Views: 4

Posted: 12.07.2025

Expiry Date: 26.08.2025

Job Description:

Experienced Clinical Research Associate, Italy

Your responsibilities will include:

• 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, i.e., Good Clinical Practice and International Conference on Harmonization guidelines
• Managing progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutions
• Collaborating with experts at study sites and with client representatives

Qualifications:

• University Bachelor's Degree and Master's Degree in a scientific discipline or healthcare
• CRA Certification as required by Ministerial Decree dated 15.11.2011
• Experience in Pharma Industry and/or Clinical Trials environment
• Excellent command of English
• Organizational, time management, and problem-solving skills
• Ability to establish and maintain effective working relationships with coworkers, managers, and clients
• Flexibility to travel
• Driver’s license class B

What you can expect:

• Resources that promote your career growth
• Leaders that support flexible work schedules
• Programs to help you build your therapeutic knowledge
• Excellent working environment in a stable, international, reputable company
• Company car, mobile phone, and attractive benefits package

IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at IQVIA's website.