Clinical Trials & Patient Engagement

MastarRec; City Of London; On-site; GBP 40,000 - 55,000; Full time

Job summary

A clinical research organization in the City of London is seeking a detail-oriented Clinical Research Coordinator to manage clinical trial activities, ensuring compliance with GCP guidelines and study protocols. You will coordinate various aspects of clinical research, from participant recruitment to data management, in a fast-paced environment that fosters healthcare innovation and research excellence. This role offers competitive compensation, private health insurance, and a supportive work environment.

Benefits

Competitive salary with annual performance bonuses

Training and career development

Private health insurance

Pension plan

Flexible working options

Qualifications

• In-depth understanding of clinical research regulations and ethical standards.
• Experience in recruiting and consenting study participants.
• Ability to maintain accurate source documentation.

Responsibilities

• Coordinate and manage the day-to-day operations of clinical studies.
• Monitor patient safety and ensure protocol adherence.
• Prepare regulatory documentation and site initiation reports.

Skills

In-depth knowledge of GCP

Experience with clinical data collection

Proficiency with electronic data capture systems

Strong organizational and time management skills

Excellent communication and interpersonal abilities

Detail-oriented

Education

Bachelor’s degree in Life Sciences

ACRP or SOCRA certification

Tools

REDCap

Medidata

Job description

Job Description

We are seeking detail-oriented Clinical Research Coordinator (CRC) to oversee and manage clinical trial activities, ensuring strict adherence to GCP guidelines, regulatory requirements, and study protocols. You will play a critical role in coordinating all aspects of clinical research — from participant recruitment to data management and compliance monitoring — to support the delivery of groundbreaking medical advancements.

This is an exciting opportunity to work at the intersection of healthcare innovation, patient care, and research excellence in a collaborative, fast-paced environment.

Job Responsibilities

• Coordinate and manage the day-to-day operations of clinical studies
• Recruit, screen, and consent eligible study participants in accordance with IRB-approved protocols
• Maintain accurate and up-to-date source documentation and electronic data capture (EDC) systems
• Monitor patient safety, schedule study visits, and ensure protocol adherence
• Liaise with principal investigators, sponsors, and ethics committees
• Prepare regulatory documentation, site initiation, and close-out reports
• Track study progress and submit timely updates to stakeholders
• Ensure quality assurance and compliance with ICH-GCP, MHRA, and institutional regulations

Required Skills

• In-depth knowledge of GCP, clinical research regulations, and ethical standards
• Experience with clinical data collection, source documentation, and informed consent processes
• Proficiency with electronic data capture systems (e.g., REDCap, Medidata, or similar)
• Strong organizational and time management skills
• Excellent communication and interpersonal abilities
• Detail-oriented and able to handle multiple trials simultaneously

Desired Skills

• Bachelor’s degree in Life Sciences, Nursing, or Health Sciences
• ACRP or SOCRA certification
• Previous experience in oncology, cardiology, or rare disease clinical trials
• Familiarity with clinical trial software platforms and regulatory submissions

Job Benefits

• Competitive salary with annual performance bonuses
• Training and career development in clinical operations and trial management
• Private health insurance and pension plan
• Supportive work environment with flexible working options
• Work with a cross-disciplinary team of clinical and research experts