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CTI Clinical Trial and Consulting Services
CTI Clinical Trial and Consulting Services
1,001 – 5,000 Employees
BiotechnologyConsultingHealthcare
CTI Clinical Trial and Consulting Services is a contract research organization serving biotechnology and pharmaceutical sponsors throughout the clinical development process. Its work spans clinical trial execution, regulatory strategy, laboratory and bioanalytical services, real-world evidence, and research center management across Phase I–IV studies. CTI brings experience in areas such as rare diseases, cell and gene therapy, oncology, neurology, and transplantation, supporting study design, site management, patient recruitment, monitoring, safety and pharmacovigilance, biometrics, and quality assurance. The company combines integrated trial services with patient-focused research and global regulatory guidance.
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Senior Clinical Research Associate II – UK Remote

Senior Clinical Research Associate II overseeing UK clinical trial sites for CTI Clinical Trial and Consulting Services. The role includes site visits, remote monitoring, enrollment support, and regulatory compliance.

GBUnited KingdomRemoteFull-timeSeniorEnglish RequiredClinical Research
Google Cloud Platform

Description

  • Act as CTI’s primary contact for assigned clinical trial sites
  • Carry out pre-study, site initiation, interim monitoring, and close-out visits
  • Deliver all site visit documentation in line with the Monitoring Plan and required deadlines
  • Support or lead study start-up, feasibility, pre-study, and site selection activities
  • Gather, review, and maintain essential and regulatory documentation
  • Complete required training and attend investigator, client, and project team meetings
  • Develop and execute subject enrollment plans for assigned sites
  • Oversee the storage, dispensing, and accountability of investigational products and trial materials
  • Manage site activities and report site status to the Clinical Project Manager
  • Perform remote monitoring in accordance with the study-specific Monitoring Plan
  • Use systems and reports to monitor subject status, CRF retrieval, source document review, regulatory records, and investigational products
  • Contribute to project-specific work as a member of the Project Team

Requirements

  • Three to five years of clinical research experience as a CRA or in a related profession
  • Background in life sciences
  • Strong knowledge of ICH-GCP and applicable regulatory requirements
  • Ability to conduct pre-study, site initiation, interim monitoring, and close-out visits
  • Ability to complete site visit deliverables within required deadlines
  • Knowledge of applicable regulations, standard operating procedures, and ICH-GCP
  • Ability to support or oversee study start-up, feasibility, pre-study, and site selection activities
  • Ability to collect, review, and track essential and regulatory documents
  • Ability to complete required general and study-specific training
  • Ability to participate in investigator, client, and project team meetings, including presentations
  • Ability to develop and implement subject enrollment strategies
  • Ability to manage investigational products and trial-related materials
  • Ability to conduct site management and remote monitoring activities
  • Ability to use systems and reports to track subject status, CRF retrieval, source document review, regulatory documents, and investigational products

Benefits

  • Structured mentoring program
  • Leadership development courses
  • Dedicated training department
  • Support for continuing education
  • Hybrid work opportunities
  • CTI Cares community and global giving opportunities
  • Work contributing to the development of life-changing treatments

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