Senior Research Coordinator: Clinical Trials Leader

Great Ormond Street Hospital; Greater London; Hybrid; GBP 40,000 - 55,000; Full time

Benefits offered by this job

Flexible working

Help with childcare and travel

Training and development opportunities

Assistance with finding somewhere to住

Live-in support

Job summary

Great Ormond Street Hospital in London is seeking a Senior Research Coordinator to join our dynamic research team. You will lead on coordinating a portfolio of complex pediatric and rare disease studies and ensure timely study setup, budgeting, and data reporting in line with robust protocols.

Working with lead consultants and lead research nurses, you will manage regulatory submissions, start-up activities, and the maintenance of research databases, including IRAS, to support high-quality

Qualifications

• Educated to degree level or equivalent (eg, medical, biomedical, administration / management).
• Postgraduate degree (or equivalent experience).
• GCP knowledge and understanding.
• Experience in a clinical trial environment within NHS, pharma or university.
• Experience in staff management and development, clinical supervision and mentoring.
• Experience costing / managing the process of commercial clinical research.

Responsibilities

• Coordinate a portfolio of complex studies with lead consultants and lead research nurses.
• Lead on study costing and pipeline tracking with robust data reporting.
• Prepare regulatory submissions and manage regulatory documentation.
• Organise start-up activities and meetings; arrange patient visits and investigations.
• Coach, mentor and supervise research coordinators and administrators.

Skills

Verbal and written communication

Organisation and time management

Team coordination

Project coordination

Stakeholder management

Education

Degree level or equivalent

Postgraduate degree

Tools

IRAS

Databases

Job description

Great Ormond Street Hospital in London is seeking a Senior Research Coordinator to join our dynamic research team. You will lead on coordinating a portfolio of complex pediatric and rare disease studies and ensure timely study setup, budgeting, and data reporting in line with robust protocols.

Working with lead consultants and lead research nurses, you will manage regulatory submissions, start-up activities, and the maintenance of research databases, including IRAS, to support high-quality