12 часов назад
Clinical Trials Scientific Affairs Supervisor
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Clinical Trials Scientific Affairs Supervisor (Clinical Trials/Scientific Affairs): Managing pre-award clinical trial testing reviews, referral laboratory coordination, pricing documents, and scientific responses for RFPs and RFIs with an accent on team leadership, regulated laboratory operations, and cross-functional delivery. Focus on determining protocol testing requirements, coordinating referral laboratories, improving operational processes, and resolving study-related testing issues.
Location: Remote, United Kingdom
Company
provides laboratory and scientific services supporting clinical trials and regulated testing activities.
What you will do
- Manage daily department performance, resources, workload prioritization, staffing capacity, and operational metrics.
- Lead, coach, train, and develop direct reports, including onboarding, performance management, and career development.
- Review clinical trial protocols to determine testing requirements, testing facilities, methods, and associated referral laboratory needs.
- Prepare and review pricing documents and provide scientific and technical information for client RFPs and RFIs.
- Coordinate with Commercial, Operations, Scientific, Sales, HR, referral laboratories, and external clients to resolve study and testing issues.
- Lead process improvements, update SOPs, maintain templates and tools, and support root cause analysis and operational efficiency.
Requirements
- Must be based in the United Kingdom while working remotely.
- Bachelor’s degree in a relevant scientific discipline or at least 3 years of experience as a Clinical Laboratory Scientist.
- At least 5 years of laboratory experience in a clinical setting or relevant regulated environment.
- Strong interpersonal, communication, time-management, organizational, and multitasking skills.
- Ability to work independently and collaboratively, lead and motivate others, and manage projects with tight deadlines.
- Proficiency in Microsoft Office and respect for patient confidentiality and company procedures.
Nice to have
- Generalist laboratory experience.
- MT (ASCP) certification.
- A positive, solutions-oriented mindset.
Culture & Benefits
- Full-time schedule of 37.5 hours per week, Monday through Friday during daytime hours.
- Remote work arrangement within the United Kingdom.
- Work involving cross-functional collaboration, continuous education, coaching, and professional development.
- Sedentary, primarily office-based role requiring prolonged computer work and sustained concentration.
- Some roles may require flexible hours, TB screening, or a valid driver’s license.
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