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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.
