Clinical Trial Liaison
3 weeks ago
Αθήνα, GRI, Ελλάδα
TFS
Πλήρης απασχόληση
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Assignment type: Freelance consultancy contract via TFS HealthScience
Are you the person investigators call back? We are looking for a Clinical Trial Liaison for a freelance assignment with one of our biopharma clients, supporting an ongoing clinical programme in Europe.
This is a site facing role, not a monitoring role. You are the local link between the sponsor, the CRO team and the investigator sites, and you are measured on one thing: sites that activate on time, enrol, and stay engaged.
What You Will Do
- Build and hold strong relationships with investigators and site staff in your market
- Bring local insight into feasibility, site selection and country enrolment planning
- Run site motivation and enrolment support visits, and step in early when a site slips
- Support start up, regulatory and EC submission activities with local knowledge
- Attend Site Initiation Visits as sponsor representative and carry out oversight visits covering both CRA and site performance
- Work with the CRO team on a shared plan for trial targets, and escalate site issues with a proposed solution Engage patient advocacy groups and KOLs where they matter to recruitment Who You Are
- Life science degree
- 7+ years in clinical research, at least 5 as CRA, monitor or equivalent
- Proven site management background and an established investigator network in your country
- Experience from specialty indications
- Strong ICH GCP knowledge
- Fluent English plus your local language
- Used to working across CTM, start up, medical and CRO teams Clinical or medical background is an advantage Practical
- Freelance consultancy contract through TFS HealthScience
- Part time, scope and duration confirmed at interview
- Travel to sites required Rate discussed openly at the first conversation About TFS HealthScience TFS is a global mid-size CRO. We work with biotech and pharma clients across Europe and the US, and our consultants come back to us because we are direct about scope, rate and expectations. TFS HealthScience is a global, mid-sized contract research organization (CRO) partnering with biotechnology and pharmaceutical companies across the full clinical development lifecycle. Our expertise spans full-service clinical development, project-based support, strategic resourcing, and Functional Service Provider (FSP) solutions, matching experienced professionals to roles where they deliver the greatest impact.
- Build and hold strong relationships with investigators and site staff in your market
- Bring local insight into feasibility, site selection and country enrolment planning
- Run site motivation and enrolment support visits, and step in early when a site slips
- Support start up, regulatory and EC submission activities with local knowledge
- Attend Site Initiation Visits as sponsor representative and carry out oversight visits covering both CRA and site performance
- Work with the CRO team on a shared plan for trial targets, and escalate site issues with a proposed solution Engage patient advocacy groups and KOLs where they matter to recruitment Who You Are
- Life science degree
- 7+ years in clinical research, at least 5 as CRA, monitor or equivalent
- Proven site management background and an established investigator network in your country
- Experience from specialty indications
- Strong ICH GCP knowledge
- Fluent English plus your local language
- Used to working across CTM, start up, medical and CRO teams Clinical or medical background is an advantage Practical
- Freelance consultancy contract through TFS HealthScience
- Part time, scope and duration confirmed at interview
- Travel to sites required Rate discussed openly at the first conversation About TFS HealthScience TFS is a global mid-size CRO. We work with biotech and pharma clients across Europe and the US, and our consultants come back to us because we are direct about scope, rate and expectations. TFS HealthScience is a global, mid-sized contract research organization (CRO) partnering with biotechnology and pharmaceutical companies across the full clinical development lifecycle. Our expertise spans full-service clinical development, project-based support, strategic resourcing, and Functional Service Provider (FSP) solutions, matching experienced professionals to roles where they deliver the greatest impact.