Question
Full-time
5-10

Clinical Trial Liaison

12/12/2025

The Clinical Trial Liaison acts as a specialized liaison to assist sites with patient identification and recruitment processes. They coordinate patient recruitment plans, provide support to project teams, and track patient enrolment progress throughout the study.

Working Hours

40 hours/week

Company Size

1,001-5,000 employees

Language

English

Visa Sponsorship

No

About The Company
PSI is a leading full-service global Contract Research Organization whose key strength is predictable patient enrollment across multiple therapeutic areas. PSI is known in the industry as a CRO focused on ‘on-time project delivery’. This is achieved through investing substantial effort and MD resources into performing quality feasibility assessments that provide an accurate predictor of study timelines. PSI’s global reach allows us to run clinical trials across multiple continents, in 50+ countries around the world. PSI’s reputation is that of a 'no-nonsense'​ CRO focused on timely patient enrollment and project delivery. An exceptionally high repeat and referral business rates alongside low staff turnover are indicative of our commitment to be the best CRO in the world as measured by our clients and our employees. http://www.psi-cro.com
About the Role

Company Description

PSI is a leading Contract Research Organization with 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.

    Job Description

    Only CV's in English will be considered

    In this role, a Clinical Trial Liaison: 

    • Acts as a specialized liaison to assist sites with a protocol-tailored approach to increase efficiency of the patient identification and recruitment process. 
    • Assists sites in developing and implementing patient enrolment techniques. 
    • Coordinates site specific patient recruitment and retention plans observing the planned metrics.
    • Provides information specific to the area of expertise to site team members involved in patient recruitment.
    • Identifies, tracks, and reports patient enrolment progress throughout the study.
    • Analyses the protocol in order to provide the site with the support needed to improve the patient pathway.
    • Provides support to the project teams to ensure proper documentation of study-specific assessments related to patient enrolment.
    • Assists and advises the site monitor in the area of patient enrolment.
    • Provides information related to patient enrolment to Business Development to use for proposals.
    • Prepares for and attends Bid Defense Meetings.
    • Attends and presents at Investigator’s Meetings

    This role requires approximately 35% travel. 

    Qualifications

    • Registered Nurse (RN) or equivalent associate degree
    • A minimum of 5 years of experience 
    • Experience in operation and QC procedures related to the equipment used in the specialized area
    • Advanced level of English 
    • Proficiency in standard MS Office applications
    • Proficiency in relevant PSI in-house application

    Additional Information

    All your information will be kept confidential according to EEO guidelines.

    Key Skills
    Clinical TrialsPatient RecruitmentPatient RetentionProtocol AnalysisDocumentationProject SupportCommunicationTeam CollaborationNursingMS OfficeData TrackingPatient PathwayBid Defense MeetingsInvestigator MeetingsQuality ControlPatient Enrolment Techniques
    Categories
    HealthcareScience & ResearchConsulting
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