Senior CRA - Ireland based sites

ICON; Monza; In loco; EUR 35.000 - 55.000; Tempo pieno

Descrizione del lavoro

A leading global clinical research organization seeks a Senior Clinical Research Associate to oversee oncology studies. You will utilize your strong CRA expertise and prior experience in a dynamic role that includes data management, investigator recruitment, and compliance with regulations. This position requires travel, ensuring that study integrity is maintained while fostering a culture of process improvement.

Servizi

Competitive salary

Range of health insurance offerings

Various annual leave entitlements

Employee Assistance Programme

Flexible optional benefits

Competenze

• 3-4 years of independent monitoring experience desired.
• Ability and willingness to travel.
• Expert knowledge of ICON's SOPs / WPs, ICH, GCP and appropriate regulations.

Mansioni

• Coordinate activities required to set up and monitor a study.
• Ensure accuracy and completeness of data entered into ICON systems.
• Maintain timelines and ensure timely submission of protocol/consent documents.

Conoscenze

Attention to detail

Process Improvement

Knowledge of ICH/GCP

Independent coordination

Patient confidentiality

Descrizione del lavoro

As a Senior CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. This role is focused on Oncology studies within a Biotechnology sponsor. Please note that we are looking for strong CRA's with 3-4 years of prior experience.This role will be travelling across Ireland.

• Recognize, exemplify and adhere to ICONs values which centre on our commitment to People, Clients and Performance.
• As a member of staff, the employee is expected to embrace and contribute to our culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs.
• Ability and willingness to travel
• Expert knowledge of ICON's SOPs / WPs, ICH, GCP and appropriate regulations.
• Familiarity with ICON systems
• Maintain timelines. Ensure accuracy and completeness of data entered into ICON systems.
• Recruitment of investigators.
• Independent and proactive coordination of all the necessary activities required to set up and monitor a study, including but not limited to the following :
• Identify investigators.
• Help when requested, in preparation of regulatory submissions.
• Design of patient information sheets and consent forms.
• Ensure timely submission of protocol / consent documents for ethics / IRB approval. Pre study / placement and initiation visits. Conduct regular monitoring visits in accordance with the ICON
• site monitoring SOP / sponsor site monitoring SOP, as appropriate
• Maintain all files and documentation pertaining to studies. Motivate investigators in order to achieve recruitment targets. Complete accurate study status reports.
• Ensure the correct storage of drugs and the diligent account of all drugs in accordance with SOPs.
• Keep the Project Manager regularly informed.
• Process case record forms to the required quality standards and timelines. Deal with sponsor generated queries in a timely manner.
• Ensure the satisfactory closeout of investigator sites.
• Participate, if requested, in the preparation of and review of study documentation, e.g. draft protocols, draft CRFs, monitoring guidelines and elements of final report.
• Participate in feasibility studies for new proposals as required. Ensure correct archiving of files on completion of a study.
• Maintain patient and sponsor confidentiality.
• Assume additional responsibilities as directed by the Project Manager.
• investigational Products (IPs) stored and managed by the site :

o Ensure storage conditions and acceptable supplies are provided

o Ensure IPs are supplied only to eligible patients o Ensure IP receipt, use and return are controlled and documented

o Ensure disposition of unused IP comply with regulatory requirement and are in accordance with the sponsor.

o Act in a lead role on a study assuming additional responsibilities as detailed / documented by the Project Manager if appropriate

Participate in data listing reviews, as applicable.

• Participate in training and mentoring new staff up to Clinical Research Associate level as appropriate.
• Assist with marketing the company if and when appropriate.
• Other duties as assigned.

You are :

• 3-4 years if independent monitoring experience desired
• Ability to travel across Ireland

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.

• 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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