Clinical Research Coordinator (1 yr contract) - Central/GOVT/ENTRY LEVEL #HAO

Recruit Express Pte Ltd.; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

An established industry player is seeking a Clinical Research Coordinator to manage and oversee research projects. This role involves coordinating study start-up activities, ensuring compliance with regulatory standards, and facilitating smooth project execution. The ideal candidate will possess a degree in Life Sciences and have a strong understanding of clinical research processes. Join a dynamic team dedicated to advancing healthcare research and make a significant impact in the field. If you're passionate about research and eager to contribute to meaningful projects, this opportunity is perfect for you.

Qualifications

• Degree in Life Sciences or similar required.
• Strong knowledge of GCP, ICH guidelines, and regulatory standards.

Responsibilities

• Coordinate study start-up activities and workflow.
• Monitor research quality and compliance with guidelines.
• Assist with study closure and archiving activities.

Skills

Clinical Research Coordination

Data Collection

Regulatory Compliance

Communication Skills

Education

Degree in Life Sciences

Job description

Clinical Research Coordinator (1 yr contract) - Central/GOVT/ENTRY LEVEL #HAO

Salary: up to $4000
Duration: 1 year direct contract

Working Days & Hours: Mon-Fri Office Hours

Location: Novena

Job Description:
Pre-Study

1. Coordinate study start-up activities, including assisting with feasibility reviews and furnishing of regulatory documents

2. Plan, organize and coordinate the workflow of the study

3. Development of materials and tools required for study start-up

4. Coordinate all mandatory training requirements and documentation

Study Recruitment and Conduct

1. Assisting with informed consent process by providing information to and educating research subjects, data collection and surveys

2. Coordinate all relevant subject visits, ensuring minimum deviation from schedule of visits

3. Ensure projects can be completed within the time frame and facilitate smooth running of research projects

4. Assist PI to ensure timely amendments to study documents when required

Study Monitoring, Audit and Inspection

1. Monitor the quality of research ensuring compliance with HBRA, GCP, ICH guidelines and standards

2. Conduct monitoring visits including Remote Monitoring and Site Monitoring

3. Assist with all external monitoring, audit and inspection visits

4. Monitor the financial aspects of the assigned study and advise the stakeholders accordingly

5. Work with PI and department to respond to any audit findings and implement approved recommendations

Study Closure

1. Assist withstudy closure activities including archival and assisting with all audits/ inspections/ monitoring

2. Ensuring proper closure of study with all ethics and regulatory authorities

3. Ensuring proper archiving of all study records including medical records, study documents, investigator files, subject files etc

Job Requirements: Min Degree in Life Sciences or similar

Interested candidates, please submit your resume to: [e-mail]

Ally Audrey Lok Xin Woon

Recruit Express Pte Ltd (Healthcare & Lifescience)