Clinical Trials Study Coordinator — Patient-Centric

St Pancras Clinical Research; Eastbourne; On-site; GBP 27,000 - 33,000; Full time

Job summary

A clinical research organization in Eastbourne is seeking a Study Coordinator to manage and administer ongoing clinical trials. The role involves ensuring adherence to research protocols, delivering high-quality data, and maintaining patient care standards. Candidates should have a minimum of 1 year clinical research experience and strong knowledge of Good Clinical Practice (GCP). This full-time position offers a starting salary of £30,000 per annum, depending on experience.

Qualifications

• Minimum 1 year of clinical research coordinator experience.
• Strong understanding of ICH Good Clinical Practice.
• Flexible and can do attitude.

Responsibilities

• Manage all aspects of allocated clinical trials.
• Deliver timely, efficient and high-quality clinical trial data.
• Ensure the highest standard of care for patients.

Skills

Clinical research coordination

Good Clinical Practice (GCP)

Patient-centric approach

Microsoft Office applications

Data management

Team player

Job description

A clinical research organization in Eastbourne is seeking a Study Coordinator to manage and administer ongoing clinical trials. The role involves ensuring adherence to research protocols, delivering high-quality data, and maintaining patient care standards. Candidates should have a minimum of 1 year clinical research experience and strong knowledge of Good Clinical Practice (GCP). This full-time position offers a starting salary of £30,000 per annum, depending on experience.