Clinical Trial Site Coordinator - Data Entry & Recruitment

TFS HealthScience; Pamplona; Presencial; EUR 28.000 - 38.000; Jornada completa

Descripción de la vacante

TFS HealthScience is seeking a Site Coordinator to support study sites and facilitate PI-led trials across Dermatology, Neuroscience, Oncology and Ophthalmology. You will handle data entry, ensure timely queries resolution, and aid with SAE notifications while supporting patient recruitment.

As part of the SRS/FSP team, you will collaborate with a sponsor and participate in ethics submissions, monitoring visits, and investigator meetings. Travel to sites is expected as needed.

Formación

• Bachelor’s degree in life sciences or proven data-entry experience.
• Excellent organizational skills with ability to prioritize multiple tasks.
• Willingness to travel and adapt to changing priorities.
• Strong written and verbal English communication skills.

Responsabilidades

• Data Entry.
• Queries resolution.
• Assist with SAE notification.
• Help investigator with patient recruitment.
• Facilitate Ethics Committee submissions.
• Attend Monitoring Visits, Audits and Inspections as required.
• Investigator File updating.
• Patient visits scheduling.
• Study Drug Accountability and Dispensing logs.
• Assist in investigators meetings or training.

Conocimientos

Data entry

Organizational skills

English communication

Travel availability

Educación

Bachelor’s Degree in life science

Descripción del empleo

TFS HealthScience is seeking a Site Coordinator to support study sites and facilitate PI-led trials across Dermatology, Neuroscience, Oncology and Ophthalmology. You will handle data entry, ensure timely queries resolution, and aid with SAE notifications while supporting patient recruitment.

As part of the SRS/FSP team, you will collaborate with a sponsor and participate in ethics submissions, monitoring visits, and investigator meetings. Travel to sites is expected as needed.