Clinical Research Coordinator / Assistant

JOBSTUDIO PTE. LTD.; Glasgow; On-site; GBP 25,000 - 35,000; Full time

Job summary

A leading company in Glasgow seeks a Clinical Research Coordinator/Assistant to support impactful healthcare research. The role involves coordinating clinical trials, ensuring regulatory compliance, and engaging with research teams to enhance study operations. Candidates with a background in science or healthcare are encouraged to apply, offering a chance to grow in a dynamic environment.

Benefits

Opportunities for training and professional growth in clinical research operations.

Be part of community-focused clinical research with real impact on patient care.

Qualifications

• Diploma or Degree in a science or healthcare-related field.
• Experience in clinical research is an advantage.
• Familiarity with GCP, medical terminology, and research processes preferred.

Responsibilities

• Coordinate and assist in clinical research trials in compliance with study protocols and regulations.
• Screen potential participants based on eligibility criteria and assist in recruitment.
• Perform data entry, update tracking logs, and maintain research records.

Skills

Good Clinical Practice (GCP)

Medical terminology

Research processes

Education

Diploma or Degree in a science or healthcare-related field

Job description

Are you passionate about contributing to impactful healthcare research that directly benefits the community? We are seeking a dedicated Clinical Research Coordinator/Assistant to support and coordinate the conduct of clinical research studies in compliance with regulatory requirements and international research standards.

Key Responsibilities:

• Coordinate and assist in the conduct of clinical research trials in compliance with study protocols, Good Clinical Practice (GCP), and applicable regulations.
• Screen potential participants based on eligibility criteria and assist investigators in participant recruitment and the informed consent process.
• Schedule, monitor, and follow up on study visits according to protocol requirements to ensure participant compliance and safety.
• Create and manage source documents, case report forms (CRFs), and other research documentation to ensure data integrity and regulatory compliance.
• Perform timely and accurate data entry, update tracking logs, and maintain secure and organized research records.
• Report adverse events, abnormal results, or protocol deviations to Principal Investigators and relevant research teams, and assist with follow-up actions.
• Coordinate and support site monitoring visits and audits, and assist in implementing corrective actions as needed.
• Liaise with research teams, clinic departments, and collaborators to ensure smooth study operations and logistics.
• Assist with ethics board and regulatory submissions, budget tracking, and multi-site study coordination when required.
• Provide administrative and operational support, including meeting preparation, documentation, and study-related materials.

Requirements:

• Diploma or Degree in a science or healthcare-related field
• Experience in clinical research is an advantage
• Familiarity with Good Clinical Practice (GCP), medical terminology, and research processes is preferred

Why Join Us?

• Be part of community-focused clinical research with real impact on patient care
• Gain valuable experience in a dynamic, multidisciplinary research environment
• Opportunities for training and professional growth in clinical research operations

How to Apply:

Interested applicants, kindly furnish us with your detailed resume in MS Words format and click "Apply Now" button

** We regret to inform only shortlisted candidates will be notified. Applicants who do not possess necessary experience or qualification will still be considered on individual merits and may be contacted for other opportunities.**

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JOBSTUDIO PTE LTD

EA License No: 10C4754

EA Personnel: Hoh Mei Ling

EA Personnel Reg No: R21103150