Business & Project Intelligence
Site Management Services
Phase 1, Early Phase & Clinical Pharmacology Trial Management
Contract Research Services
Whilst investigators have the ultimate responsibilities in clinical studies, clinical research coordinators (CRCs) are key members of study teams and usually play an important role in the success of clinical studies.
HKU-CTC has a team of professional CRCs who are ready to offer support to investigators and study sites through HKU-CTC’s CRC service – CRISP (Clinical Research Investigative Site Professionals). All CRCs are certified under PRACTISE® Core – an ICH GCP investigator site personnel training program program meeting the minimum criteria of TransCelerate BioPharma – and are well-trained on relevant SOPs and site operational skills. HKU-CTC’s robust management structure ensures close supervision of each CRC’s performance and full backup among the team of CRCs, whilst maintaining accountability to investigators at study sites. Terms of engagement are flexible and can be tailored for meeting investigators’ needs.
|Qualified CRCs certified by PRACTISE® Core an ICH GCP investigator site personnel training program meeting the minimum criteria of TransCelerate BioPharma|
|Systematic and comprehensive SOPs and operational training evidenced by complete training records|
|Robust management structure supporting close supervision by supervisors and full backup by a team of CRCs|
|Accountable to investigators whilst assuming duties at study sites|
|Flexible terms of engagement|