Clinical Research Coordinator: Drive Impactful Trials

Recruit Express Pte Ltd; Singapore; On-site; SGD 52,000 - 75,000; Full time

Job summary

Recruit Express Pte Ltd seeks a Clinical Research Coordinator to support clinical studies and deliver high-quality research outcomes. You will coordinate recruitment, screening, enrolment and follow-up, while ensuring adherence to study protocols, GCP and regulatory requirements.

Collaborating with investigators and study teams, you will maintain source data, complete CRFs, manage study documents, and escalate issues promptly.

Qualifications

• Degree in Science, Life Sciences, Public Health, Health Sciences, Pharmacy, Medicine or Nursing.
• Experience in clinical research or related setting is advantageous.
• Familiarity with GCP, regulations and ethical principles in human biomedical research.
• Strong organisational skills to manage multiple study activities and timelines.
• Meticulous and detail-oriented with data accuracy and documentation focus.
• Good analytical, communication and interpersonal skills.
• Able to work independently and collaboratively in a multidisciplinary team.

Responsibilities

• Coordinate participant recruitment, screening, enrolment and follow-up activities per study protocol.
• Work with the Principal Investigator and study team to support recruitment and site performance.
• Review study protocols, eligibility criteria and study requirements with clinical staff and participants.
• Facilitate informed consent processes and protect participant rights and confidentiality.
• Maintain source documentation and review clinical data for completeness and accuracy.
• Complete and manage Case Report Forms (CRFs) and regulatory documentation.
• Identify missing or inconsistent information and follow up for clarification.
• Maintain essential study files, participant records, regulatory documents and logs.
• Coordinate study supplies and management of investigational products where applicable.
• Monitor and document adverse events and protocol deviations, escalating as required.
• Ensure activities and documentation meet timelines and protocol/site procedures.
• Develop study-specific documentation or source templates when required.
• Communicate protocol-related matters and study updates to the team.
• Participate in investigator meetings and study team meetings.
• Liaise with the PI and management on study-specific matters.
• Support research activities across satellite clinic sites when required.
• Uphold ethical, legal, regulatory and confidentiality requirements throughout studies.

Skills

Organisational skills

Attention to detail

Data accuracy

Communication skills

Teamwork

Education

Bachelor's degree in Life Sciences

Job description

Recruit Express Pte Ltd seeks a Clinical Research Coordinator to support clinical studies and deliver high-quality research outcomes. You will coordinate recruitment, screening, enrolment and follow-up, while ensuring adherence to study protocols, GCP and regulatory requirements.

Collaborating with investigators and study teams, you will maintain source data, complete CRFs, manage study documents, and escalate issues promptly.