Clinical Research Associate, Sponsor Dedicated - Italy

Experteer Italy; Town of Italy (NY); Remote; USD 70,000 - 90,000; Full time

Job summary

A leading clinical research firm is seeking an experienced Clinical Research Associate to effectively manage clinical trial sites in New York. Responsibilities include performing site visits, supporting recruitment planning, and ensuring compliance with regulatory standards. Candidates must have a Bachelor’s and Master’s degree in a relevant field and CRA Certification. This is a full-time position offering a flexible work environment and competitive benefits.

Benefits

Company car

Mobile phone

Attractive benefits package

Qualifications

• University degree in a relevant field required.
• CRA Certification needed as per regulations.
• Experience in Pharma Industry or Clinical Trials is a plus.

Responsibilities

• Perform site selection, initiation, monitoring, and close-out visits.
• Support development of a subject recruitment plan.
• Evaluate site practices against regulatory standards.

Skills

Excellent command of English language

Organizational skills

Time management

Problem-solving skills

Very good computer skills including MS Office

Ability to establish effective relationships

Flexibility to travel

Education

University Bachelor's Degree and Master's Degree in scientific discipline or health care

CRA Certification as required by Ministerial Decree

Job description

Overview

Experienced Clinical Research Associate, Italy

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

Company summary

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

Location: Milan, Italy

Type: Full time