3 часа назад
Clinical Scientist (Clinical Research)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Clinical Scientist (Clinical Research): Supporting global clinical trials and electronic Clinical Outcome Assessment solutions with an accent on scientific leadership, endpoint quality, and operational excellence. Focus on analyzing study performance, resolving clinical data integrity issues, delivering rater training, and advising sponsors on clinical outcome assessments and endpoint strategy.
Location: Remote in the United Kingdom; international travel of approximately 10–20% may be required.
Company
, part of Thermo Fisher Scientific, develops electronic Clinical Outcome Assessment solutions that support global clinical research and the development of life-changing therapies.
What you will do
- Serve as the primary scientific contact for assigned international clinical trials and provide scientific leadership to sponsors, investigative sites, and internal stakeholders.
- Co-lead study execution with Project Management teams, maintaining scientific integrity, operational excellence, milestones, and deliverables.
- Monitor study metrics and create analyses, dashboards, and reports covering trends, risks, outliers, and mitigation strategies.
- Identify and resolve clinical quality, endpoint quality, and data integrity issues in line with study requirements and GCP.
- Develop and deliver rater training, calibration activities, and remediation programs.
- Advise on clinical outcome assessments, study design, endpoint strategy, protocol implementation, scoring methodologies, and scientific interpretation.
Requirements
- Graduate degree in Life Sciences, Psychology, Neuroscience, Clinical Research, Public Health, Pharmacy, or a related scientific discipline.
- At least 5 years of experience in the clinical research industry and at least 3 years in a client-facing scientific role such as Clinical Scientist or Clinical Trial Science Lead.
- At least 4 years of experience supporting the administration, training, or oversight of clinical outcome assessments, rating scales, or study endpoints.
- Demonstrated neuroscience experience and comprehensive knowledge of clinical trial methodology, study execution, endpoint quality management, research methods, data interpretation, and applied statistics.
- Strong knowledge of Good Clinical Practice, ICH guidelines, and clinical research regulations.
- Fluent English, strong communication and presentation skills, and the ability to manage multiple studies and stakeholder relationships in a global environment.
Culture & Benefits
- Competitive compensation and incentives.
- Private health, pension, and life insurance.
- Flexible time off and hybrid work options.
- Employee programs and modern technology for remote collaboration.
- Opportunities to contribute to scientific research, publications, conference presentations, SOPs, and operational improvements.
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