Remote Clinical Research Job at IQVIA | CRA Job in Italy
A rare chance has emerged for professionals seeking a remote clinical research job at IQVIA in Italy. This position offers an opportunity to work from home while contributing to vital clinical research efforts. Interested candidates are encouraged to apply soon.
Job Details
- Position: Clinical Research Associate, Site Management
- Location: Milan, Italy – Remote
- Reference Number: R1540967
- Salary: €33,900.00 – €61,700.00 annually
About IQVIA
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. The organization is dedicated to creating intelligent connections that accelerate the development and commercialization of innovative medical treatments, ultimately improving patient outcomes and population health worldwide. With a strong presence in Italy, IQVIA is committed to maintaining high standards in clinical research and site management.
Remote Clinical Research Job Description
The Clinical Research Associate will perform monitoring and site management work to ensure that sites are conducting studies and reporting data as required. This role is essential in maintaining compliance with study protocols, applicable regulations, and sponsor requirements.
Eligibility Criteria for Remote Clinical Research Job
- Master’s Degree in Life Sciences.
- Possession of CRA certification according to Ministerial requirements.
- Completion of CRA training program or prior monitoring experience.
- Basic knowledge of clinical research regulatory requirements (GCP and ICH guidelines).
- Proficiency in Microsoft Word, Excel, and PowerPoint.
- Strong written and verbal communication skills, with a good command of English.
- Excellent organizational and problem-solving skills.
- Able to establish effective working relationships with coworkers, managers, and clients.
Remote Clinical Research Job – Key Responsibilities
- Conduct site monitoring visits including selection, initiation, monitoring, and close-out visits in accordance with regulatory requirements.
- Collaborate with sites to adapt and track subject recruitment plans to enhance predictability.
- Administer protocol training to assigned sites and maintain regular communication to manage project expectations.
- Evaluate the quality and integrity of study site practices and escalate issues as necessary.
- Manage study progress by tracking regulatory submissions, recruitment, and data query resolution.
- Ensure proper documentation is maintained in accordance with Good Clinical Practice (GCP) and local regulations.
- Generate regular visit reports and collaborate with study team members for project execution.
- Support development of project subject recruitment plans and manage site financials as needed.
This remote clinical research job at IQVIA presents an excellent opportunity for qualified candidates seeking a CRA job in Italy. With a commitment to improving patient outcomes and a supportive work environment, IQVIA encourages interested individuals to apply before the deadline to take the next step in their clinical research careers.
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