Clinical Research Nurse: Study Coordinator & Participant Care

Velocity Clinical Research, Inc; Lublin; On-site; PLN 85,000 - 120,000; Full time

Job summary

Velocity Clinical Research, Inc is seeking a Clinical Research Nurse to coordinate and conduct clinical studies while delivering high-quality participant care in line with study protocols, GCP/ICH guidelines, MHRA requirements, and SOPs. Role blends advanced nursing with trial management to support participant safety, protocol compliance, and data integrity.

The successful candidate will provide direct nursing care, administer IMPs per protocol, support recruitment and study visits, and

Qualifications

• Registered Nurse qualification.
• Current registration with the Nursing and Midwifery Council (NMC).
• Minimum of 2 years of post-registration nursing experience.
• Experience working within a healthcare environment involving direct patient care.

Responsibilities

• Coordinate and conduct clinical research studies in accordance with approved protocols, UK GCP, ICH-GCP guidelines, MHRA requirements, and Company SOPs.
• Provide direct nursing care to research participants throughout all phases of study participation.
• Perform protocol-required clinical procedures, including venepuncture, cannulation, vital signs assessment, ECGs, clinical assessments, drug preparation and administration, and specimen collection and processing.
• Administer investigational medicinal products (IMPs) in accordance with protocol requirements and nursing scope of practice.
• Monitor participants for adverse events (AEs), SAEs, and AESIs, ensuring timely reporting and escalation.
• Conduct informed consent discussions and support ongoing participant understanding and consent throughout study participation.
• Coordinate participant scheduling and study visits.
• Support participant recruitment, screening, enrolment, retention, and follow-up activities.
• Maintain accurate source documentation and ensure timely and complete data entry into sponsor and vendor electronic systems.
• Resolve data queries and collaborate with sponsors, CROs, and study teams to support data quality.
• Support protocol implementation, study start-up activities, amendments, and close-out processes.
• Maintain accountability for participant safety and protocol compliance.
• Assist with regulatory document preparation, maintenance, and submission as required.
• Collaborate effectively with investigators, sponsors, CROs, pharmacies, laboratories, and other healthcare professionals.
• Mentor and support junior clinical staff and research personnel as appropriate.
• Contribute to quality improvement initiatives and study process enhancements.
• Promote respect for cultural diversity and maintain a participant-centred approach to care.
• Perform other duties as assigned.

Skills

Clinical assessment

GCP knowledge

Research methods

Communication skills

Organization

Independent work

Attention to detail

Team collaboration

EDC systems

Problem solving

Education

Nursing qualification

NMC registration

Tools

MS Office

EDC systems

Job description

Velocity Clinical Research, Inc is seeking a Clinical Research Nurse to coordinate and conduct clinical studies while delivering high-quality participant care in line with study protocols, GCP/ICH guidelines, MHRA requirements, and SOPs. Role blends advanced nursing with trial management to support participant safety, protocol compliance, and data integrity.

The successful candidate will provide direct nursing care, administer IMPs per protocol, support recruitment and study visits, and