Clinical Trial Liaison

PSI CRO; São Paulo; Presencial; BRL 120.000 - 160.000; Tempo integral

Resumo da oferta

A leading Clinical Research Organization in São Paulo is seeking a Clinical Trial Liaison who will act as a liaison to enhance patient identification and recruitment. This role involves coordinating site-specific recruitment plans, tracking enrolment progress, and working closely with site teams. Candidates must have at least 5 years of experience, advanced proficiency in English, and familiarity with MS Office. The position requires approximately 35% travel and focuses on delivering quality service across therapeutic areas.

Qualificações

• Minimum of 5 years of experience required.
• Advanced English proficiency is essential.
• Familiarity with operation and QC procedures.

Responsabilidades

• Act as a liaison for site assistance.
• Implement patient recruitment strategies.
• Coordinate recruitment plans and metrics.
• Track and report patient enrolment progress.
• Advise on patient pathways and support project teams.

Conhecimentos

Patient recruitment techniques

Protocol analysis

Documentation

Communication

Team coordination

Ferramentas

MS Office

PSI in-house application

Descrição da oferta de emprego

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

• 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.