10 дней назад
Senior Laboratory Project Services Coordinator (Clinical Research)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Senior Laboratory Project Services Coordinator (Clinical Research): Coordinating laboratory activities across clinical studies, including study setup, site loading, investigator portal access, kit shipments, monitoring, and closeout, with an accent on protocol-specific requirements, centralized laboratory monitoring, and stakeholder communication. Focus on identifying performance trends, resolving study issues and escalations, supporting audits and training, and improving laboratory processes and documentation.
Location: Singapore
Company
provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.
What you will do
- Support project managers with study setup, planning, meeting minutes, action logs, laboratory instructions, monitoring plans, and reports.
- Coordinate study activities including site loading, investigator portal access, kit shipments, daily performance monitoring, and laboratory centralized monitoring.
- Manage queries, protocol questions, issues, and escalations with internal and external stakeholders.
- Review study outputs and reports to identify trends and provide feedback on investigator site and service performance.
- Coordinate customer communications, project launch meetings, training sessions, audits, inspections, and investigator or client meetings.
- Contribute to process improvement projects, SOP revisions, document quality control, and junior staff mentoring.
Requirements
- Bachelor’s degree in life sciences or a related field, or an equivalent combination of education, training, and experience.
- 1–3 years of relevant experience, preferably in clinical, medical, or healthcare environments.
- Proficiency in Mandarin is required due to the global portfolio.
- Good command of English is required for written and verbal communication.
- Strong interpersonal, communication, organizational, time management, critical thinking, and problem-solving skills.
- Computer proficiency in word processing, presentation, and spreadsheet applications, with the ability to manage competing priorities in a fast-paced environment.
Culture & Benefits
- Work across internal and external teams supporting global clinical studies.
- Opportunities to participate in internal and external meetings, audits, inspections, and training activities.
- Involvement in process improvement initiatives and SOP development.
- Work aligned with organizational standards, protocol requirements, and customer expectations.
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