Clinical Research Associate, Sponsor Dedicated - Italy

IQVIA; Milano; In loco; EUR 40.000 - 55.000; Tempo pieno

Vantaggi offerti da questo lavoro

Company car

Mobile phone

Attractive benefits package

Resources that promote career growth

Support for flexible work schedules

Descrizione del lavoro

A global leader in clinical research services is seeking a Clinical Research Associate in Milan, Italy. The role involves performing site monitoring, supporting subject recruitment, and ensuring compliance with regulatory standards. Candidates should have a Bachelor's and Master's degree in a relevant field, CRA certification, and experience in the Pharma industry. This full-time position offers an excellent working environment with attractive benefits including a company car and mobile phone.

Competenze

• Experience in Pharma Industry and/or Clinical Trials environment.

Mansioni

• Perform site selection, initiation, monitoring and close‑out visits.
• Support the development of a subject recruitment plan.
• Evaluate the quality and integrity of site practices.
• Manage progress by tracking regulatory submissions and data query resolutions.
• Collaborate with experts at study sites and client representatives.

Conoscenze

Very good computer skills including MS Office

Excellent command of English language

Organizational skills

Time management skills

Problem-solving skills

Flexibility to travel

Ability to establish and maintain effective working relationships

Formazione

University Bachelor's Degree in scientific discipline or health care

Master's Degree in scientific discipline or health care

CRA Certification as required by Ministerial Decree dated 15.11.2011

Descrizione del lavoro

Clinical Research Associate, Sponsor Dedicated – Italy

Join to apply for the Clinical Research Associate, Sponsor Dedicated – Italy role at IQVIA

Responsibilities

• 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 scientific discipline or health care
• In possession of CRA Certification as required by Ministerial Decree dated 15.11.2011
• Experience in Pharma Industry, and/or Clinical Trials environment
• Very good computer skills including MS Office
• Excellent command of English language
• 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 stabile, international, reputable company
• Company car, mobile phone and attractive benefits package

Seniority level

Mid‑Senior level

Employment type

Full‑time

Job function

Research, Analyst, and Information Technology

Industries

Hospitals and Health Care

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 https://jobs.iqvia.com