Senior Clinical Trials Coordinator—Drive Protocols & Impact

Kings College London; Greater London; On-site; GBP 40,000 - 60,000; Full time

Job summary

Kings College London is seeking a Senior Study Coordinator (internal) to support clinical research activities in London. You will manage study coordination tasks, ensure compliance with governance and regulatory requirements, and liaise with multidisciplinary teams and study sites.

Ideal candidates have a health sciences degree, knowledge of ICH-GCP and related regulations, and strong communication skills to facilitate protocol delivery and patient-facing processes.

Qualifications

• First degree in health sciences or related discipline.
• Knowledge of ICH-GCP, R&D Governance, EU Clinical Trials Directive and Medicines for Human Use (Clinical Trials) Regulations.
• Ability to acquire detailed protocol knowledge and communicate protocol requirements to both professionals and patients.
• Knowledge of research ethics and governance frameworks and ability to facilitate research applications.
• More than two years' experience as a Clinical Trials Coordinator, Clinical Project Manager or equivalent clinical research role.
• Experience working independently and as part of multidisciplinary teams, with excellent interpersonal and communication skills.

Responsibilities

• (Not explicitly stated in the HTML)

Skills

Two+ years clinical trials experience

ICH-GCP & regulatory knowledge

Protocol knowledge transfer

Research ethics and governance

Interdisciplinary teamwork

Independent working

Education

Bachelor's degree in health sciences or related field

Additional trial qualification (desirable)

Job description

Kings College London is seeking a Senior Study Coordinator (internal) to support clinical research activities in London. You will manage study coordination tasks, ensure compliance with governance and regulatory requirements, and liaise with multidisciplinary teams and study sites.

Ideal candidates have a health sciences degree, knowledge of ICH-GCP and related regulations, and strong communication skills to facilitate protocol delivery and patient-facing processes.