Clinical Research Coordinator

MastarRec; Manchester; On-site; GBP 38,000 - 52,000; Full time

Job summary

A healthcare research organization is looking for a detail-oriented Clinical Research Coordinator to manage clinical trial activities in Manchester. The role involves coordinating participant recruitment, managing data compliance, and ensuring adherence to GCP guidelines. Candidates should possess a Bachelor's degree in Life Sciences and have strong communication skills. This full-time position offers a competitive salary between £38,000 and £52,000, along with professional development opportunities.

Benefits

Competitive salary with annual performance bonuses

Training and career development

Private health insurance

Pension plan

Flexible working options

Qualifications

• Knowledge of clinical research regulations and ethical standards.
• Ability to handle multiple trials simultaneously.

Responsibilities

• Coordinate and manage the day-to-day operations of clinical studies.
• Recruit, screen, and consent eligible study participants.
• Monitor patient safety schedule and ensure protocol adherence.
• Track study progress and submit timely updates to stakeholders.

Skills

In-depth knowledge of GCP

Experience with clinical data collection

Proficiency with electronic data capture systems

Strong organizational skills

Excellent communication abilities

Detail-oriented

Education

Bachelor's degree in Life Sciences, Nursing, or Health Sciences

ACRP or SOCRA certification

Job description

Job Description

We are seeking a 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

Requirements

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

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

Employment Type: Full Time

Experience: years

Vacancy: 1

Yearly Salary: 38,000 - 52,000