Research Coordinator

Borr Drilling; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

A leading company in drilling services is seeking a Research Coordinator to manage and oversee clinical studies. The role involves ensuring adherence to protocols, managing budgets, and collaborating with the research team for efficient project execution. Candidates should possess a Bachelor's Degree in Sciences or Public Health and have relevant clinical research experience.

Benefits

Good career growth

Personal development opportunities

Qualifications

• Strong written communication skills are required.
• Experience in clinical research is necessary.

Responsibilities

• Manage study budgets, track expenditures, and oversee site operations.
• Support PI in study preparations and perform participant screenings.
• Ensure compliance with regulatory and ethical requirements.

Skills

Clinical research

Communication

Data integrity

Education

Bachelor's Degree in Sciences

Public Health or equivalent

Job description

• Contract full time position (Renewable)
• Office hours
• Good career growth and personal development

As a Research Coordinator, you will be responsible for the following duties:

• Manage study budgets where applicable, including tracking expenditures and ensuring appropriate utilization of funds.
• Oversee and coordinate multi-site study operations, ensuring alignment across participating locations.
• Monitor project milestones and timelines; coordinate regular reviews with the study team and Clinical Research Unit (CRU).
• Support the PI in preparing study-related presentations, documents, and communication materials.
• Contribute to the evaluation and interpretation of research findings when required.
• Study Conduct Coordination:
• Perform participant screening in accordance with protocol eligibility criteria and assist with recruitment efforts.
• Schedule and coordinate study visits, ensuring adherence to protocol-defined timelines and visit schedules.
• Stay updated with current regulatory, ethical, and institutional requirements; perform delegated, protocol-specific tasks in compliance with these guidelines.
• Monitor and promptly report adverse events, unanticipated problems, and protocol deviations to the PI and CRU. Ensure timely and appropriate reporting to regulatory authorities, granting bodies, and IRBs, as applicable.
• Maintain data integrity and ensure accurate, organized, and complete study documentation.
• Collaborate closely with the research team to facilitate efficient project execution. Attend team meetings to discuss study progress and review collected data.

Requirements

• Bachelor's Degree in Sciences, Public Health, or equivalent.
• Experience in clinical research and strong written communication skills

To apply, simply click on the ‘’apply’’ button in the job advertisement or alternatively, you can send in your resume via email:
Email Address: [e-mail]

We regret to inform that only shortlisted candidates will be notified.

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