Clinical Research Lead
Employment Information
Report this job
Job expired or something wrong with this job?
Job Description
Clinical Research Lead managing investigators, sites, enrollment, and vendor oversight for ICON’s sponsor-dedicated clinical research programs in the UK.
Responsibilities:
- Manage clinical Investigators and sites considered and/or participating in the client’s clinical trials and Post Marketing Safety Studies
- Identify and qualify Investigators and sites
- Deliver clinical trial enrollment in accordance with scientific objectives
- Deliver database locks on time
- Manage issues at clinical trial sites
- Ensure inspection readiness for assigned therapeutic areas
- Manage Investigators and sites comprehensively using information and tools to support informed decisions
- Interact with global clinical trial sites to drive a high-quality customer experience
- Oversee vendor monitoring activities at clinical trial sites
- Identify, mitigate, and escalate significant findings and trends
- Perform hybrid Lead CRA and junior management tasks
- Manage stakeholders and collaborate on clinical research activities
Requirements:
- BA / BS/ BSc in the sciences or RN is required and preferred
- Bachelor's degree in life sciences or a related field
- Experience in oversight of external vendors (CROs, central labs, imaging vendors, etc.)
- Strong investigator-sponsored study experience gained within the industry at a clinical trial manager level
- Previous experience as a Senior CRA (Clinical Research Associate)
- Previous experience in clinical research, site management, or a related field preferred
- Strong interpersonal and communication skills
- Excellent organizational and problem-solving skills
- Knowledge of ICH-GCP guidelines and regulatory requirements for clinical trials
- Previous experience in a biotech, pharmaceutical or CRO company is preferred
- Travel on average 6 times per month
- Valid and current UK working eligibility
- Legal right to work in the country where the role is based
Benefits:
- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways
Similar Jobs
Clinical Research Development Analyst
Clinical Research Development Analyst supporting clinical trial strategies, protocols, and regulatory dossiers. Contributing to new medicine approvals and clinical data generation at Libbs Farmacêutica.
Early Clinical Scientist – Translational Medicine
Early Clinical Scientist coordinating early-phase clinical trials for Parexel’s clinical development services. Overseeing safety, data validity, CRO performance, and trial documentation.
Clinical Trial Manager, Class III Medical Devices
Clinical Trial Manager coordinating Class III implantable-device trials at Biogen, a biotechnology company. Managing sites, vendors, compliance, risks, and regulatory workflows.
Clinical Research Associate II
Clinical Research Associate II monitoring oncology clinical trials for PSI, a contract research organization. Managing site visits, data integrity, regulatory documents, and investigator communications.
Clinical Research Site Manager, Neurology
Clinical Research Site Manager overseeing startup, enrollment, compliance, and performance across neurology clinical-trial sites for Johns Hopkins University. Remote role based in the Baltimore, Maryland area.
Biostatistician, Neurology
Biostatistician analyzing longitudinal neurology data for Johns Hopkins School of Medicine. Developing SAS/R analyses, datasets, statistical plans, and publication-ready results.
Senior Clinical Research Associate
Senior Clinical Research Associate monitoring clinical trials for Precision for Medicine, a specialized clinical research organization. Coordinating study setup, site visits, regulatory compliance, client support, and junior staff mentoring.
Senior Clinical Research Associate
Senior Clinical Research Associate monitoring clinical trials for Precision for Medicine, a specialized CRO. Ensuring protocol compliance, site oversight, and sponsor collaboration across Spain.
Senior Clinical Research Associate
Senior Clinical Research Associate monitoring clinical trials for Precision for Medicine, a specialized CRO. Coordinating study setup, site monitoring, regulatory activities, clients, and junior CRA mentoring.
Clinical Research Associate II
Clinical Research Associate II advancing AbbVie’s oncology clinical trials. Monitoring investigative sites, protecting patient safety, and improving data integrity for innovative medicines.
Clinical Trial Manager, Regulatory Experience
Clinical Trial Manager overseeing site monitoring, regulatory compliance, and clinical data quality for Syneos Health’s biopharmaceutical research services. Supporting trial delivery, audits, recruitment, and site teams.
Clinical Trial Manager
Clinical Trial Manager overseeing study start-up, CRAs, vendors, budgets, and clinical deliverables. Supporting Linical’s CRO mission to provide clinical-trial expertise.
Senior Clinical Research Associate
Senior Clinical Research Associate at AbbVie, a biopharmaceutical company developing innovative medicines and health solutions. Overseeing clinical study sites, monitoring, regulatory compliance, audits, and CRA mentoring in Taiwan.
Clinical Research Associate II – Immunology
Clinical Research Associate monitoring immunology clinical trials for AbbVie, an innovative medicines company. Ensuring site compliance, data integrity, patient safety, and recruitment performance.
Senior Clinical Research Associate
Senior Clinical Research Associate monitoring vaccine trials for ICON, a global clinical research organisation. Overseeing sites, compliance, data integrity, and trial execution in Buenos Aires remotely.
Clinical Research Site Manager, Neurology
Clinical research site manager coordinating startup, enrollment, compliance, and performance across neurology trials for Johns Hopkins University. Remote role managing external clinical sites and investigators.
Clinical Research Associate II, Bilingual
Clinical Research Associate monitoring pharmaceutical trials for protocol compliance and data integrity. Conducting remote and on-site site visits across Canadian investigational sites.
Senior Biostatistician
Senior Biostatistician supporting ophthalmic clinical trial design, analysis, and reporting at Lexitas. Ensuring statistical integrity across clinical studies, submissions, and publications.
Clinical Research Feasibility Coordinator
Clinical research coordinator assessing trial feasibility, investigators, site capabilities, and budgets for Alcanza’s multi-site clinical research network. Supporting Business Development across Phase I-IV studies.
Clinical Research Associate II – Sponsor-dedicated
Clinical Research Associate monitoring clinical trial sites for Syneos Health, a fully integrated life sciences services organization. Ensuring GCP compliance, data integrity, and study delivery.