Rare Disease Clinical Nurse Practitioner – Research Expert

Medpace; Cincinnati (OH); On-site; GBP 70,000 - 110,000; Full time

Benefits offered by this job

Flexible work

Competitive compensation

Competitive PTO

Career growth

Employee events

Health & wellness

Job summary

Medpace seeks Advanced Nurse Practitioners/Clinical Nurse Specialists with Rare Disease experience to support clinical research studies alongside physicians as clinical experts. Role involves reviewing safety data and contributing to study design and proposals, with no direct patient care.

Strong medical management and non-medical prescribing experience are preferred. Join a global CRO with a collaborative environment, offering growth opportunities across oncology, CNS, and metabolic diseases

Qualifications

• Masters or Doctorate in nursing or equivalent qualifications.
• Active Nursing and Midwifery Council registration with NMC PIN.
• Significant experience as a clinical nurse practitioner or nurse consultant in Rare Diseases.
• Clinical research experience preferred.
• Evidence of autonomous clinical or research work at senior level.

Responsibilities

• Develop and implement disease-specific and clinical education for internal teams.
• Review study and study participant clinical safety data as part of medical monitoring.
• Review protocols for scientific and participant safety matters and risks.
• Attend pre-study and study-related meetings, providing clinical expertise.
• Assist Clinical Operations with recruitment, screening and conduct activities.
• Participate in new business activities by providing clinical input in proposals.
• Serve as a clinical expert in business presentations to clients.

Skills

Clinical nursing

Rare diseases experience

Autonomous clinical work

Clinical research experience

Education

Masters or Doctorate in Nursing

Job description

Medpace seeks Advanced Nurse Practitioners/Clinical Nurse Specialists with Rare Disease experience to support clinical research studies alongside physicians as clinical experts. Role involves reviewing safety data and contributing to study design and proposals, with no direct patient care.

Strong medical management and non-medical prescribing experience are preferred. Join a global CRO with a collaborative environment, offering growth opportunities across oncology, CNS, and metabolic diseases