Clinical Research Fellow
Core
Coordinate and manage clinical trial activities, including regulatory submissions, patient screening, consent facilitation, and data documentation within a hospital trust.
Role type
Clinical Research Fellow (Medical)
Builds
Clinical trials for vaccines, flu/RSV, and specialty-based research
Domain
Healthcare / Clinical Research
Deliverable
client delivery
Required skills
Regulatory approval submission, patient screening, informed consent facilitation, clinical risk management, evidence-based practice, audit participation, prioritization
Preferred skills
Prior NHS experience, publications, prizes and honours, logical thinking, problem-solving
Technologies
None explicitly stated
Responsibilities
Submit applications for Regulatory, Ethics and Governance permissions; Identify and screen local patients against inclusion/exclusion criteria; Initiate and facilitate informed consent processes; Maintain accurate auditable documentation; Identify barriers to recruitment and facilitate resolution; Participate in team meetings and academic education sessions
Seniority
Mid-level, hands-on IC