Experienced Clinical Research Associate, IQVIA Biotech - Home based, Italy

IQVIA Argentina; Milano; In loco; EUR 35.000 - 50.000; Tempo pieno

Descrizione del lavoro

A global clinical research provider is seeking a Site Manager to oversee monitoring activities in clinical trials. Responsibilities include conducting site visits, ensuring regulatory compliance, and collaborating with study sites. The ideal candidate will have a Bachelor's and Master's degree in relevant fields, CRA certification, and experience in the pharma industry. Excellent English skills and strong organizational abilities are required for this role based in Milan, Italy.

Competenze

• Bachelor's and Master's degree in a relevant field.
• Certified as CRA as per local regulations.
• Experience in the Pharma or Clinical Trials environment.
• Excellent computer skills, particularly in MS Office.
• Fluent in English.
• Strong organizational and time management capabilities.
• Ability to establish effective working relationships.
• Willingness to travel.
• Valid driver's license class B.

Mansioni

• Conduct site monitoring visits and ensure compliance with GCP and ICH guidelines.
• Collaborate with sites to enhance subject recruitment.
• Administer training and maintain communication with study sites.
• Evaluate study site practices and document monitoring findings.
• Support regulatory submissions and manage study progress.
• Maintain essential documentation per regulatory standards.

Conoscenze

Site monitoring

Problem-solving

Organizational skills

Time management

Communication

MS Office

English proficiency

Formazione

University Bachelor's Degree

Master's Degree in scientific discipline or healthcare

CRA Certification

Descrizione del lavoro

Job 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) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP 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

• 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

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