Clinical Research Associate FREELANCE

TFS HealthScience; Roma; In loco; EUR 30.000 - 50.000; Part-time

Descrizione del lavoro

A global Contract Research Organization is seeking a Clinical Research Associate for a freelance position in Italy. You will be responsible for monitoring clinical trials, ensuring compliance with regulatory standards, and addressing site issues. The ideal candidate holds a degree in life sciences, has a minimum of 2 years of experience as a CRA, and possesses excellent communication and organizational skills. This role offers a competitive compensation package and opportunities for growth.

Servizi

Competitive compensation package

Comprehensive benefits

Opportunities for personal and professional growth

Competenze

• Minimum 2 years of experience working as a CRA.
• Experience in clinical trial site monitoring.
• Familiarity with Good Clinical Practice regulations and ICH guidelines.

Mansioni

• Monitor on-site clinical trials according to regulatory requirements.
• Review CRFs and source documentation for accuracy.
• Identify site problems and initiate corrective actions.

Conoscenze

Excellent written and verbal communication skills

Excellent organizational skills

Ability to work independently and in teams

Experience in Neuroscience

Ability and willingness to travel

Formazione

Bachelor's Degree in life science or nursing

Descrizione del lavoro

CRA ITALY - FREELANCE - 0.5 FTE OCTOBER / NOVEMBER 2025 URGENT!

The role

The Clinical Research Associate (CRA) is part of Strategic Resourcing Solutions Unit within TFS Develop and will function operationally as a member of a Project Team and is responsible for the initiation, on‑site and remote monitoring and termination of investigative sites during study conduct, according to company policies, SOPs and regulatory requirements. The CRA may conduct all stages of site monitoring (feasibility, pre‑study, initiation, interim, and close‑out). Ability to travel as needed : may involve overnight and international travel.

Responsibilities

• Monitor on‑site clinical trials in accordance with TFS and / or client company Standard Operating Procedures, FDA regulations, and GCP and ICH guidelines
• Review CRFs (paper or electronic) and subject source documentation for validity and accuracy and generate queries to investigational sites / clients to resolve problem data
• Identify site problems / deficiencies and bring to the attention of management through trip reporting, memos, and verbal communication with Project Manager or Lead CRA
• Initiates corrective action to resolve issues as directed by supervisor
• Contribute to the completion of the application to Ethics Committee / IRB, prepare necessary documentation enclosed to the application according to local requirements in cooperation with CTA and directed by Lead CRA / Project Manager
• Participate in contract handling and negotiation directed by Lead CRA / Project Manager
• Set up ISF and SMF (or cooperate with CTA) and distribute to the investigational sites.
• In cooperation with study team, responsible for SMF maintenance
• Order, ship, and reconcile clinical investigative supplies for study sites, if applicable
• Order, ship and coordination of study supplies at site
• May prepare and submit status reports as directed by Lead CRA / PM
• Review and support site staff to maintain SMF
• Review Informed Consent documents for essential elements and protocol specifics
• Update CTMS system with site and study information
• May audit data in tables and text of clinical summaries
• May assist in the preparation of study documentation such as CRF Completion Guidelines, patient diaries, study participation cards by reviewing for accuracy and completeness
• Prepare check requisitions for sponsor Project Manager approval, when applicable

Qualifications

• Bachelor’s Degree, preferably in life science or nursing; or equivalent
• Minimum 2 years of experience working as a CRA
• Experience in Neuroscience, desirable
• Used to working by metrics
• Able to work in a fast paced environment with changing priorities
• Understand basic medical terminology and science associated with the assigned drugs and therapeutic areas
• Possess the understanding of Good Clinical Practice regulations, ICH guidelines
• Ability to work independently as well as in a team matrix organization
• Excellent written and verbal communication skills.
• Excellent organizational skills
• Ability and willingness to travel

What We Offer

We provide a competitive compensation package, comprehensive benefits, and the opportunity for personal and professional growth in a rewarding environment. You’ll be joining a team that values collaboration, innovation, and making a difference in the lives of patients.

A Bit More About Us

Our journey began over 27 years ago in Sweden, in the city of Lund. As a full‑service, global Contract Research Organization (CRO), we build solution‑driven teams working towards a healthier future. Bringing together over 800 professionals, TFS delivers tailored clinical research services in more than 40 countries with flexible clinical development and strategic resourcing solutions across key therapeutic areas including Dermatology, Neuroscience, Oncology, and Ophthalmology.

Our core values of Trust, Quality, Passion, Flexibility, and Sustainability are our guiding light serving as the framework for decision‑making at all levels of the organization. They assist us in attracting and retaining valuable talent who share our sentiments, resulting in high employee engagement and satisfaction. By aligning on these fundamental values, we cultivate a unified force, geared towards innovation and excellence. This collective effort propels us towards our shared goal and fosters a culture of mutual respect and collaboration. Together we make a difference.