Lead Clinical Research Associate

TFS HealthScience; Remoto; EUR 40.000 - 60.000; Part-time

Descrizione del lavoro

A global mid-size Contract Research Organization is seeking a Lead CRA Freelance for a remote position (0.5 FTE) in Italy. The role involves overseeing monitoring and site management activities, leading and training CRAs, and ensuring compliance with clinical guidelines. Candidates should possess a Bachelor's Degree in life science or nursing, have a minimum of 3 years of CRA experience, and be familiar with oncology studies. Competitive compensation and benefits are offered, with a supportive work environment focused on innovation and patient outcomes.

Servizi

Competitive compensation package

Comprehensive benefits

Professional growth opportunities

Competenze

• Minimum 3 years of experience as CRA including relevant on-site monitoring experience.
• Experience in Phase 4 / RWE / Non-Interventional Studies.
• Understanding of Good Clinical Practice regulations, ICH guidelines.
• Excellent organizational and Line Management skills.
• Ability and willingness to travel up to 10-20%.

Mansioni

• Oversee all aspects of monitoring and site Management activities.
• Lead, manage and guide CRAs.
• Development of Study Monitor plans and training plans.
• Serve as initial point of contact for the monitoring team.
• Ensure compliance with ICH/GCP guidelines and protocols.

Conoscenze

Bachelor’s Degree in life science or nursing

Minimum 3 years of experience as CRA

Experience in Phase 4 / RWE / Non-Interventional Studies

Experience in Oncology

Understanding of Good Clinical Practice regulations

Excellent written and verbal communication skills

Ability to work independently and in a team

Organizational and Line Management skills

Formazione

Bachelor’s Degree in life science or nursing or equivalent

Descrizione del lavoro

LEAD CRA FREELANCE 0.5 FTE - REMOTE (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.

Key Responsibilities

Support the Project Manager being responsible and accountable for overseeing all aspects of monitoring and site Management activities ensuring compliance with ICH/GCP guidelines, SOPs and protocol requirements.

Lead, manage and guide CRAs being responsible for training and quality oversight of site management activities while proactively identifying potential operational issues and ensuring study deliverables.

Development of Study Monitor plans, Monitor and Site Training plans, verification initiatives, coordinating Study Investigator Meetings and reviewing site and country Study Reports.

Ensure study processes, procedures and expectations correspond to the practicality of conducting the trial from study feasibility through to close out.

Serve as initial point of contact for the monitoring team and support them with investigative site personnel liaison.

Implement monitoring/recruitment plans and support also the design of CRF completion guidelines.

Perform co-monitoring visits as part of the monitoring team quality oversight.

Reviewand approve site visit reports (PSV, SIV, MV and COV) and act as first point of contact for issue escalation ensuring the proper resolution and action plan definition and follow up.

Review CRA Site Visits calendar ensuring monitoring visits (both remotely and on site) are being scheduled and conducted following monitoring plan frequency.

Update the Project Manager with status of sites and countries and ensure a proper escalation of any issue detected at site/country level.

Ensure documents remain current during the course of the trial and ensure proper maintenance of Trial Master File being responsible of QC when delegated by Project Manager.

When delegated by Project Manager, track and approve investigators payments.

Assist Project Manager in CRA training program, training CRAs on study procedures and requirements and ensuring a proper handover when there is a replacement of CRA.

Qualifications

Bachelor’s Degree, preferably in life science or nursing; or equivalent

Minimum 3 years of experience as CRA including relevant on-site monitoring experience.

Experience in Phase 4 / RWE / Non-Interventional Studies

Experience in Oncology, ideally Breast Cancer

Understand the 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 and multiple projects

Excellent written and verbal communication skills as well as computer skills

Excellent organizational and Line Management skills

Ability and willingness to travel up to 10-20%

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.