Enable job alerts via email!

Clinical Research Coordinator II

Singapore National Eye Centre

Singapore

On-site

SGD 60,000 - 80,000

Full time

30+ days ago

Generate a tailored resume in minutes

Land an interview and earn more. Learn more

Start fresh or import an existing resume

Job summary

An established industry player is seeking a Clinical Research Coordinator II to support clinical research studies at a prominent institute. In this role, you will be responsible for coordinating study-related activities, including subject recruitment and data management. Your contributions will ensure compliance with clinical protocols and regulatory requirements while collaborating with various stakeholders. This position offers a dynamic environment where your skills in communication and organization will be key to advancing important research initiatives. If you are passionate about making a difference in the field of clinical research, this opportunity is perfect for you.

Qualifications

  • Bachelor's degree in Life Sciences or Psychology required.
  • Strong communication and interpersonal skills essential.

Responsibilities

  • Perform study-related activities like screening and recruitment of study subjects.
  • Assist in data collection, management, and manuscript writing.

Skills

Good communications skills
Interpersonal skills

Education

Bachelor's degree in Life Sciences
Bachelor's degree in Psychology

Job description

Press Tab to Move to Skip to Content Link

Select how often (in days) to receive an alert:

National Neuroscience Institute of Singapore

Clinical Research Coordinator II

Job Category: Research

Posting Date: 19 Mar 2025

You will provide research support service to the investigators in the conduct and implementation of clinical research studies and clinical trial at the National Neuroscience Institute (TTSH campus), in adherence to Singapore Guideline for Good Clinical Practice (SGGCP) and protocol requirements.

Responsibilities

  1. Perform study-related activities, such as screening and recruitment of study subjects; assist with obtaining informed consent; coordination of subject visits; and other procedures such as administration of functional assessments and study-related questionnaires, blood-taking (if required).
  2. Assist in data collection and data management, data analysis and manuscript writing.
  3. Assist in all administrative requirements including submission process to IRB and/or regulatory authority.
  4. Work closely with internal and external stakeholders to ensure all study-related activities are carried out efficiently.

Requirements

  1. Bachelor's degree in Life Sciences, Psychology or related fields
  2. Good communications and interpersonal skills
Get your free, confidential resume review.
or drag and drop a PDF, DOC, DOCX, ODT, or PAGES file up to 5MB.