Clinical Research Associate, Site Management - Italy

IQVIA LLC; Lombardia; In loco; EUR 40.000 - 60.000; Tempo pieno

Descrizione del lavoro

IQVIA LLC is looking for a Clinical Research Associate for site management in Milan, Italy. The role involves conducting monitoring visits, managing study progress, and ensuring adherence to regulatory requirements. Candidates should hold a Master's Degree in Life Sciences and have CRA certification. Strong communication and organizational skills, along with some experience in clinical research, are crucial. The position offers a full-time opportunity to contribute to advancements in medical treatments.

Competenze

• Master's Degree in Life Sciences required.
• CRA certification per Ministerial requirements is mandatory.
• Prior monitoring experience or CRA training is necessary.
• Familiarity with GCP and ICH guidelines.
• Good command of the English language, both spoken and written.

Mansioni

• Conduct monitoring visits and ensure compliance with study protocols.
• Manage study progress and maintain project documentation.
• Train site staff and manage ongoing project expectations.
• Evaluate site practices and escalate quality issues as necessary.
• Collaborate with study team members for project execution.

Conoscenze

Clinical Research Regulation Knowledge

Organizational Skills

Problem-Solving Skills

Written and Verbal Communication Skills

Time Management

Formazione

Master's Degree in Life Sciences

Strumenti

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Laptop and iPhone/iPad

Descrizione del lavoro

Clinical Research Associate, Site Management - Italy page is loaded## Clinical Research Associate, Site Management - Italylocations: Milan, Italy: Milan, Italytime type: Full timeposted on: Posted Todayjob requisition id: R1540967Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.Essential Functions • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. • Work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability. • Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues. • Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate. • Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase. • Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) verify that the Investigator's Site File (ISF) is maintained in accordance with GCP / ICH and local regulatory requirements. • Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation. • Collaborate and liaise with study team members for project execution support as appropriate. • If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis. • If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.Qualifications • Master's Degree in Life Sciences.• In possession of CRA certification according to Ministerial requirements. • Completion of CRA training program or prior monitoring experience. • Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines). • Good therapeutic and protocol knowledge as provided in company training. • Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable). • Written and verbal communication skills including good command of English language. • Organizational and problem-solving skills. • Effective time and financial management skills. • Ability to establish and maintain effective working relationships with coworkers, managers, and clients.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 atIQVIA 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.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.