Clinical Research Associate

Iqvia; Torino; Remoto; EUR 30.000 - 50.000; Part-time

Descrizione del lavoro

A leading clinical research organization in Italy is seeking a freelance Clinical Research Associate (CRA) with at least 2 years of experience, particularly in oncology. The role involves monitoring clinical trials, ensuring compliance with Good Clinical Practices, and coordinating with study sites. Candidates must possess strong communication skills and the ability to build professional relationships. This position offers flexible hours, around 20 hours per week, and a contract duration of approximately 6 months.

Competenze

• Minimum of 2 years experience as a CRA.
• Experience in monitoring and/or coordinating clinical trials.
• Oncology experience needed.

Mansioni

• Participates in the investigator recruitment process.
• Coordinates activities with the site and internal departments.
• Monitors clinical trials in accordance with Good Clinical Practices.

Conoscenze

Strong knowledge of clinical research process

Excellent written and verbal communication skills

Ability to form productive professional relationships

Ability to handle several priorities

Knowledge of current GCP/ICH guidelines

Descrizione del lavoro

Overview

IQVIA HCPN has several exciting positions in Italy for freelance CRAs.

Location: Italy

Hours: around 20h per week

Contract: Freelance

Start: asap

Duration: around 6 months

Basic Functions

Participates in the preparation and execution of Phase I-IV clinical trials. Oversees the progress of clinical investigations by conducting site evaluation, initiation, and interim close out visits to sites. Monitors clinical trials in accordance with Good Clinical Practices and procedures set forth by IQVIA Biotech and sponsors. Works closely with the Clinical Trial Manager (CTM) and / or Lead CRA to ensure all monitoring activities are conducted according to study requirements.

Responsibilities

• Participates in the investigator recruitment process, performing site evaluation visits of potential investigators to evaluate the capability of the site to successfully manage and conduct the clinical study.
• Coordinate activities with the site and internal departments in preparation for the initiation of the study. Performs study initiation activities, reviewing with the site personnel the protocol, regulatory issues, study procedures, and provides training on completion of the eCRF and EDC system

• Monitoring activities and study close-out activities.
• Assists in resolving any issues to ensure compliance with site file audits in conjunction with ISS.
• Assures adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures through on-site monitoring visits. Performs validation of source documentation as required by sponsor. Prepares monitoring reports and letters per the timelines defined in IQVIA Biotech SOPs.
• Documents accountability, stability and storage conditions of clinical trial materials as required by sponsor. Performs investigational product inventory.
• Reviews the quality and integrity of the clinical data through (1) in house review of electronic CRF data and (2) on-site source verification and works with sites to resolve data queries and produce robust data.
• May review protocols, eCRFs, study manuals and other related documents, as requested by the Clinical Trial Manager and / or Lead CRA.
• Serves as primary contact between IQVIA Biotech and investigator; coordinates all correspondence; ensures timely transmission of clinical data with the study site and technical reporting, as requested.
• Assists with, and attends, Investigator Meetings for assigned studies.
• Attends study-related, company, departmental, and external meetings, as required.
• Ensures all study deliverables are completed per IQVIA Biotech and study timelines.

Knowledge, Skills and Abilities

• Strong knowledge of clinical research process, including working knowledge of all functional areas of clinical trials and medical terminology.
• Minimum of 2 years experience as a CRA
• Experience in monitoring and / or coordinating clinical trials required.
• Oncology experienced needed
• Excellent written and verbal communication skills to express complex ideas to study personnel at research and clinical institutions.
• Able to form productive professional relationships both internally within own function, cross-functionally and externally with health care professionals.
• Able to handle several priorities within multiple, complex trials.
• Able to reason independently and recommend specific solutions in clinical settings.
• Able to work independently, prioritize, and work within a matrix team environment.
• Knowledge of current GCP / ICH guidelines applicable to the conduct of clinical research.

If this role sounds of interest, please apply today!