Primary clinical point of contact with the client
Collaborate with PM on monthly invoicing and variance management of clinical budget
Develop study related clinical documents (e.g. clinical plans, Informed Consent Form templates
Identify and develop training needs for CRAs and third-party vendors specific to the study
Generate potential site list from key stakeholders and drive site feasibility process
Identify potential risks to the enrollment targets based on feasibility analysis and site’s

🎯 Requirements

Bachelor's degree or equivalent in science or health-related field; Advanced degree preferred
Minimum of 5-8 years of clinical research experience, significant clinical monitoring experience
Experience in Phase 1 FIH and healthy volunteer clinical trials
Mandarin language proficiency required
Experience with Microsoft Office Products (Outlook, Word, Excel, PowerPoint)
Excellent communication and interpersonal skills for team interactions

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