Senior Clinical Research Associate

TFS HealthScience; Roma; Remote; EUR 53,000 - 55,000; Full time

Benefits offered by this job

Lunch vouchers

Health insurance

Pension plan

Car allowance where applicable

Job summary

TFS HealthScience is seeking a Senior Clinical Research Associate to work remotely from Italy. You will monitor sites (on-site and remote), ensure data integrity and patient safety, and support regulatory compliance across studies in collaboration with project teams.

The role requires 5+ years of trial monitoring experience, oncology exposure preferred, and strong English skills. Expect substantial travel, with a permanent contract and competitive compensation.

Qualifications

• Bachelor's Degree, preferably in life science or nursing; or equivalent.
• At least 5 years of experience monitoring clinical trials (3 years oncology – early phase desirable).
• Able to work in a fast-paced environment with changing priorities.
• Understand basic medical terminology and science related to the drugs and therapeutic areas.
• Possess knowledge of GCP regulations and ICH guidelines.
• Ability to work independently as well as in a matrix team.
• Fluent in English and excellent organizational skills.
• Willingness to travel up to 60–80%, overnight and abroad if applicable.

Responsibilities

• Monitor on-site and remote trials according to GCP/ICH and SOPs.
• Perform monitoring activities to ensure subject safety and data integrity.
• Verify informed consent and protocol compliance at sites.
• Review CRFs and source documentation for accuracy.
• Manage Investigational Product accountability and logistics as needed.
• Document monitoring visits and actions taken in reports and tracking systems.
• Provide sites with issue lists and required corrective actions.
• Ensure ISF, eTMF, and CTMS are maintained per regulations and local rules.
• Assist in audits and inspections and participate in follow-up activities.
• Order, ship, and reconcile clinical supplies for sites when applicable.

Skills

Clinical trial monitoring

GCP/ICH knowledge

English fluency

Communication skills

Travel readiness

Education

Bachelor's Degree in life sciences

Nursing degree or equivalent

Tools

CTMS

eTMF

Job description

SENIOR CRA - HOMEBASED ITALY

TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and Functional Service (FSP) solutions.

Join Our Team as a Senior Clinical Research Associate home-based in Italy

About This Role

The Clinical Research Associate (CRA) is part of Strategic Resourcing Solutions (SRS) within TFS Health Science and will function operationally as a member of a Project Team and is responsible for the initiation, on–site and/or remote monitoring, close out of study sites during study conduct, according to company policies, SOPs and GCP and ICH guidelines and other regulatory requirements.

Key Responsibilities

• Monitor on-site and remotely clinical trials in accordance with TFS and/or sponsor Standard Operating Procedures GCP and ICH guidelines and applicable regulatory regulations.
• Perform all required monitoring activities at the study sites to assess and ensure subjects safety, data integrity and quality.
• Verify the protection of study participants by informed consent procedures and protocol requirements that follow appropriate regulations.
• Review CRFs (electronic or paper) and subject source documentation for validity and accuracy
• Verify proper management and accountability of Investigational Product.
• Timely reporting of actions taken during monitoring visits in Monitoring Visit Report including findings, corrective and preventive actions already taken and update applicable tracking systems, as required; escape observed deficiencies and issues as appropriate.
• Providing site with the listing of issues identified during monitoring visit and action items which will need to be addressed in a timely manner.
• Timely delivering site documents to eTMF or paper TMF; verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and ICH guidelines and local regulatory requirements.
• Participate in audit and/or inspection, its preparation and follow-up activities, as needed.
• Order, ship, and reconcile clinical investigative supplies for study sites, if applicable
• Update CTMS and all other required by projects systems with accurate site level information

Qualifications

• Bachelor’s Degree, preferably in life science or nursing; or equivalent
• At least 5 years of experience monitoring clinical trials (3 years of experience involved in Oncology trials - early phase desirable)
• 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.
• Strong written and verbal communication skills.
• Fluent in English
• Excellent organizational skills
• Technology savvy and good software and computer skills
• Soft skills: Self-awareness, resolute, flexibility, proactivity, collaborative mindset, analytic approach, and attention to detail
• Ability and willingness to travel up to 60-80%, overnight and abroad if applicable.

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

Permanent contract

Salary: 53.000-55.000 gross/year (depending on the level of experience), in line with CCNL Terziario-Servizi (Level III), plus benefits (lunch vouchers, health insurance, pension, and car allowance where applicable

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.