Clinical Research Unit (Cru) - Mayapada Hospital Tangerang

Responsibilities :

• Coordinate clinical trial feasibility assessments and site qualification visits with Sponsors/CROs and hospital departments.

• Oversee clinical trial planning, implementation, and compliance with study protocols, GCP, and applicable regulations.

• Coordinate participant recruitment, enrollment, informed consent, safety monitoring, and adverse event reporting.

• Ensure accurate clinical trial data management, documentation, confidentiality, and recordkeeping.

• Coordinate regulatory submissions, ethics committee approvals, and clinical trial registrations.

• Manage clinical trial budgets, invoicing, fund allocation, and payments to investigators and relevant departments.

• Coordinate investigators, research staff, Sponsors/CROs, and hospital departments to ensure smooth trial operations.

• Monitor clinical trial quality and ensure proper management, storage, and accountability of investigational products and research samples.

• Monitor clinical trial KPIs, revenue and recruitment targets, investigator qualifications, and annual site development plans.

Qualifications:

• Bachelor's degree in a health-related field; medical doctors are preferred.

• 1–2 years of experience in clinical research, preferably as a Clinical Research Associate (CRA) or Study Coordinator.

• Effective verbal and written communication skills.

• Fluent in English; proficiency in additional languages is an advantage.

• Strong time management skills.

• Ability to work effectively in a team.

• Proficient in Microsoft Office, particularly Excel and PowerPoint.

• Placement : Mayapada Hospital Tangerang