Experienced Clinical Research Associate, IQVIA Biotech - Home based, Italy
Experienced Clinical Research Associate, IQVIA Biotech - Home based, Italy
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Job Description
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 Investigators 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 Bachelors Degree and Masters 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
Drivers 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
Required Experience:
Senior IC
Employment Type
Full-Time
