Clinical Trial Assistant - Payments

Pharmaceutical Research Associates, Inc; Ravenna; In loco; EUR 30.000 - 45.000; Tempo pieno

Descrizione del lavoro

A leading clinical research organization is looking for a Clinical Trial Assistant in Ravenna. You will support essential clinical trial tasks from start-up to close-out, ensuring compliance and efficiency. This role requires strong organizational skills and experience in clinical research, offering competitive benefits and a dynamic work environment.

Servizi

Various annual leave entitlements

Health insurance offerings

Competitive retirement planning

Global Employee Assistance Programme

Flexible country-specific optional benefits

Competenze

• At least 1 year of experience in biopharmaceutical clinical research.
• Experience working on clinical trials in a biotech, pharmaceutical, or CRO company.

Mansioni

• Support key clinical trial tasks ensuring compliance with timelines and regulations.
• Manage TMF filing, quality, maintenance, compliance, and oversight.
• Act as primary contact for study sites.

Conoscenze

Clinical trial process experience

Data entry skills

Formazione

BA / BS / BSc in the life sciences or RN

Descrizione del lavoro

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.

Responsibilities

The Clinical Trial Assistant (CTA) Payments is an essential part of the Local Study Team and is responsible for supporting key clinical trial tasks for assigned studies to ensure compliance with timelines, GCP, SOPs and country regulations. The role collaborates with local study team members and is responsible for multiple tasks that span from study start-up to study close-out which enables the efficient execution of clinical trials to high quality

What you will be doing :

• Development and delivery of sites’ ISF, and eISF when utilized, and act as primary point of contact for the sites and manage the Site Operations / monitor access to eISF prior to SIV
• Maintain internal Registries and systems as required
• TMF filing, quality, maintenance, compliance, and oversight
• Provide reporting to support management of clinical trials
• Provide support with audit and inspection readiness activities
• Perform customization and translation of documents as required
• Manage Physical Archiving needs as required
• Preparation of documents and communications for distribution to and collection from sites, as required

Qualifications

You are :

• BA / BS / BSc in the life sciences or RN
• Work experience in life sciences or medically related field, including biopharmaceutical clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company at least 1 year
• Clinical trial process experience
• Work involving data entry into systems / databases and / or business support role

What ICON can offer you :

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.Our benefits examples include :

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs
• Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead
• Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others

Visit our careers website to read more about the benefits of working at ICON : ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below. in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

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Clinical Trial Assistant • ravenna, Italia