Clinical Research Pmo

Siloam Hospitals Group; Tangerang; On-site; IDR 200.000.000 - 300.000.000; Full time

Job summary

A healthcare organization is seeking a Clinical Research PMO to manage clinical research operations in Tangerang. This position involves oversight of projects, ensuring compliance with ICH-GCP and internal standards. Ideal candidates will have a Bachelor's degree in a healthcare field and at least 3 years of relevant experience with strong skills in project management and regulatory compliance.

Qualifications

• Minimum 3 years of experience in clinical research operations, quality management, or PMO roles.
• Strong understanding of ICH-GCP, SOP management, and process mapping.
• Highly detail-oriented with a focus on compliance and efficiency.

Responsibilities

• Provide strategic oversight for project management and monitor interdependencies across clinical research projects.
• Liaise with department leads to ensure alignment and delivery of project benefits.
• Improve and maintain clinical trial operation processes to ensure compliance with ICH-GCP, BPOM, and internal standards.

Skills

Project management

Regulatory compliance

Quality management

Organizational skills

Communication skills

Process efficiency

Education

Bachelor’s degree in Medicine, Biomedicine, Nursing, or related field

Tools

Excel

PowerPoint

Data visualization tools

Job description

Job Description

We are looking for a Clinical Research PMO to oversee project management and ensure smooth execution of clinical research operations across the portfolio. This role will work closely with department leads to monitor progress, maintain regulatory compliance, and enhance process efficiency within the organization.

Key Responsibilities

• Provide strategic oversight for project management and monitor interdependencies across clinical research projects.
• Liaise with department leads to ensure alignment and delivery of project benefits.
• Improve and maintain clinical trial operation processes to ensure compliance with ICH-GCP, BPOM, and internal standards.
• Develop and distribute communication materials (e.g., process change updates, training decks) to stakeholders.
• Implement and track process metrics (e.g., turnaround times, compliance indicators).

Qualifications

• Bachelor’s degree in Medicine, Biomedicine, Nursing, or a related healthcare field.
• Minimum 3 years of experience in clinical research operations, quality management, or PMO roles.
• Strong understanding of ICH-GCP, SOP management, and process mapping.
• Proficient in Excel, PowerPoint, and data visualization tools.
• Excellent organizational and communication skills.
• Highly detail-oriented with a focus on compliance and efficiency.
• Placement: Head Office — Siloam Hospitals Group