Senior Clinical Research Associate - Remote/Hybrid (Contract)

Emerald Clinical Trials Inc.; Singapore; Hybrid; SGD 146,000 - 207,000; Part time

Benefits offered by this job

Competitive compensation

Hybrid or remote arrangements

Career growth and global network

Employee wellbeing programs

Job summary

Emerald Clinical Trials Inc. in Singapore seeks a Senior Clinical Research Associate (Contractor) to join the Clinical Operations group. You will oversee site monitoring, regulatory packages, and TMF maintenance to ensure compliance with SOPs and timelines.

The role requires 2–5 years of on-site monitoring experience, solid ICH-GCP knowledge, and strong communication and travel willingness. You will collaborate with investigators, ethics committees, and vendors to drive quality across trials.

Qualifications

• 2–5 years of on-site monitoring and site management experience.
• Practical knowledge of ICH-GCP guidelines and global/regional regulatory requirements.
• Strong negotiation, conflict resolution, critical thinking, and strategic thinking abilities.

Responsibilities

• Coordinate the identification, feasibility assessment, and selection of investigators and sites for the trial.
• Complete monitoring activities per the Monitoring Plan and prepare monitoring visit reports within the set timeframe.
• Plan, organize, and conduct site evaluation visits and report findings to assist site selection.
• Prepare regulatory packages and liaise with regulatory colleagues regarding import/export and Ethics Committee updates.
• Negotiate site budgets, coordinate contract execution, track invoicing, and ensure timely site payments.
• Plan and conduct site initiation visits and maintain project documents.
• Develop and maintain monitoring tools and TMF-related documents.
• Motivate and train investigators to ensure protocol and product understanding and ensure trial compliance.
• Reconcile TMF with Investigator Site Files and ensure proper filing.
• Coordinate distribution, tracking, and destruction of investigational product and trial supplies.
• Maintain trial information in the CTMS and other reporting tools; support recruitment strategies.

Skills

On-site monitoring

ICH-GCP knowledge

Site management

Negotiation

Communication skills

Travel willingness

Clinical research operations

Education

Related science or health care discipline

Tools

Clinical trial management system (CTMS)

Job description

Emerald Clinical Trials Inc. in Singapore seeks a Senior Clinical Research Associate (Contractor) to join the Clinical Operations group. You will oversee site monitoring, regulatory packages, and TMF maintenance to ensure compliance with SOPs and timelines.

The role requires 2–5 years of on-site monitoring experience, solid ICH-GCP knowledge, and strong communication and travel willingness. You will collaborate with investigators, ethics committees, and vendors to drive quality across trials.