Clinical Research Associate, 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

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

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

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is €32,200.00 - €53,400.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere.

Thank you for your interest in growing your career with us.