As a Senior Clinical Research Nurse, you will be responsible for managing and coordinating clinical trial activities within the Manchester Clinic. This includes conducting clinical procedures in compliance with Good Clinical Practice (GCP), supporting the setup and running of studies, and ensuring the smooth conduct of trials.

You will act as a mentor for Research Nurses and support staff, ensuring all clinical activities are carried out safely, accurately, and in accordance with study protocols. The role involves maintaining study documentation, liaising with sponsors and clinical teams, and contributing to the continuous improvement of research standards at 4MCS.

You’ll also play an integral role in ensuring participant safety and comfort, managing data accuracy, handling investigational products, and maintaining compliance with regulatory and company procedures. The position requires adaptability, attention to detail, and a proactive approach to both clinical and administrative tasks.

Clinical Activities

• Perform delegated clinical tasks efficiently and in accordance with study protocols

• Monitor and document patient visits, AEs/SAEs, and study-related data accurately

• Maintain clinical supplies and ensure accurate sample and drug accountability

• Support setup, conduct, and closeout of clinical studies

Patient & Customer Care

• Provide high-quality patient support and ensure participant safety

• Deliver professional, compassionate communication to patients and visitors

• Assist in educating participants about study procedures

Laboratory & Pharmacy

• Prepare and maintain laboratory materials and logs

• Handle biological samples, labeling, and shipment according to protocol

• Dispense study medications as per sponsor and regulatory requirements

Data Management

• Accurately record and verify study data in source notes and electronic systems

• Maintain Investigator Site Files (ISF) and other essential study documentation

Recruitment & Commercial Awareness

• Support patient recruitment and retention strategies

• Represent 4MCS professionally in all interactions with patients, sponsors, and partners

Professional Development

• Participate in ongoing training and maintain an up-to-date professional portfolio

• Mentor and support junior staff in developing their clinical research skills

General

• Adhere to all company and health & safety policies

• Uphold confidentiality, equality, and data protection standards

• Contribute to a positive, collaborative team culture

• Registered Nurse (RGN/RMN or BSc Nursing) with current NMC registration

• Minimum 2 years’ experience in clinical research or related healthcare field

• Sound understanding of ICH GCP and clinical trial protocols

• Strong organizational and time management skills

• Excellent communication and interpersonal abilities

• Ability to travel between sites when required and attend national/international meetings

• Comfortable working with biological samples and clinical data systems

• Ability to work under pressure and meet strict deadlines