SENIOR CLINICAL SCIENTIST

As a Senior Clinical Scientist you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
In this role you will contribute to the development and creation of clinical trial protocols following high scientific and clinical standards and applicable regulations.
Also, you will contribute to the identification, formulation and implementation of amendments to the clinical protocol.  What you will be doing.
Contribute to the creation of study-level documents, including preparation of clinical sections of key regulatory documents, such as Investigator’s Brochures, briefing books, safety updates and submission dossiers.
Contribute to the review and writing of clinical trial documents for CTR activities, and publications (if applicable).
Support pharmacovigilance activities (e.
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contributing to aggregate reports, patient narratives, attendance of pharmacovigilance monitoring meetings) Support regulatory activities, like preparation of meetings with regulatory agencies.
Produce training materials, share best practices and provide training to the broader clinical trial teams.
Support preparation and (if applicable) participate in study level meetings for example Investigator Meetings, Data Monitoring meetings, and others.
Supports and guides the development of data review strategy, ensuring that protocol-level deviations, eligibility criteria, study assessments & other aspects of the protocol are implemented consistently across the study (across countries/ sites).
This could also include support for Case Report Form (CRF) development, and implementation of data capture tools.
Perform high quality clinical data review and identify clinical data insights through ongoing patient level review and trends analysis, thereby supporting for example Interim Analysis, Database and Post Lock activities and resolution of scientific & medical issues throughout the study lifecycle.
Work to improve the quality of reviews/ insights with an emphasis on subject safety and eligibility, data integrity, trend identification, analysis and remediation, and identification of cases for medical review.
Provide insights to and facilitate data review process improvements, for example by identification of redundant reports, implementation of innovative data analysis processes and tools, and their continuous improvement.
#LI-NR1 You are.
Advanced degree in life sciences/ healthcare or clinically relevant degree.
Strong oncology/solid tumor CAR-T experience 5+ years of Clinical Scientist experience Strong familiarization with Good Clinical Practice (GCP) and drug development processes, ideally Phase 1 – 3; ideally paired with experience in Oncology / Immuno-Oncology Good knowledge of set-up, organization and execution of global clinical studies in a pharmaceutical company or contract research organization (CRO), or comparable experience within academic research institution.
Sound knowledge of principles of clinical data collection and reporting; demonstrated ability to use systems and tools (e.
., EDC systems, Excel, etc.) for data collection, analysis and reporting.
Ideally first experiences in how to improve and accelerate processes, systems and tools and drive continuous improvement.
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.