Senior Site Management Associate

As a Clinical Trial Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

You will be joining one of our global pharmaceutical clients, working within an organisation that is focused on improving lives of people with cancer through innovative targeted therapies.

What you will be doing:

• Create and maintain clinical trial documents.
• Participate in the identification, evaluation, and selection of clinical trial sites.
• Conduct data review.
• Responsible for tracking of ancillary and investigational supplies, specimens and/or imaging.
• Support CTMS and Trial Master File completeness.
• Support audit and/or inspection activities
• May manage CRO activities.
• Support Clinical Trial Manager(s). Collaborates with internal team members, Contract Research Organizations, vendors and sites.
• Work on problems of diverse scope where analysis of data requires evaluation of identifiable factors.
• Perform all duties and responsibilities in accordance with CFR, GCP/ICH Guidelines, SOPs, and other applicable guidelines.
• May contribute to process improvement initiatives and departmental projects.
• May act as mentor for less senior staff on the study.

You are:

• BA/BS or equivalent or any relevant and qualifying training with a minimum of 2+ years of relevant clinical trial management experience.
• Oncology clinical research experience
• Regional Clinical Trial Management experience
• Excellent leadership, communication, and organizational skills. Able to multi-task under limited direction and on own initiative.
• Ability to proactively handle multiple tasks, manage a diverse range of functional activities and solve problems simultaneously.
• Strong communication and inter-personal skills.
• Highly responsive and proactive, a team player
• Knowledge of CFR and GCP/ICH requirements
• Experienced in Microsoft Office Products (Word, Excel, PowerPoint, SharePoint, Teams) and other clinical trial systems (e.g., CTMS, EDC and eTMF)
• Ability and willingness to travel
• Fluency in English

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Why ICON?

Our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.

Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.

ICON, including subsidiaries, is an equal opportunity and inclusive employer and 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.

Interested 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.