Clinical Study Coordinator — Data Entry & Patient Recruitment

TFS HealthScience; Porto; Presencial; EUR 21 000 - 27 000; Tempo integral

Resumo da oferta

TFS HealthScience is seeking a Site Coordinator to support a sponsor across the clinical development lifecycle. You will perform site study tasks, data entry, assist with SAE notifications, and help with patient recruitment and ethics submissions.

Based in Porto, Portugal, you will join our SRS/FSP team, travel as needed, and collaborate with investigators to maintain study quality and meet milestones.

Qualificações

• Bachelor’s Degree, preferably in life science or proven experience in the role, only applicable when exclusively data entry tasks are going to be developed by the employee.
• Excellent organizational skills and demonstrated ability to prioritize and handle multiple competing priorities.
• Adaptability and flexibility to changing priorities, with ability to maintain demanding timelines.
• Good oral, written and communication skills in English.
• Ability and willingness to travel.

Responsabilidades

• Data Entry.
• Queries resolution.
• Assist with SAE notification.
• Help investigator with patient recruitment.
• Facilitate Ethics Committee submissions.
• Attend Monitoring Visits, Audits and Inspections, if required.
• Investigator File updating.
• Patient visits schedule.
• Study Drug Accountability and Dispensing logs.
• Patients’ expenses payment.
• Assist in investigators meetings or training when required.
• Sample Management, not including any invasive procedure or contact with dangerous samples or substances.

Conhecimentos

Organizational skills

Time management

English proficiency

Communication skills

Adaptability

Travel willingness

Formação académica

Bachelor’s degree in life sciences

Descrição da oferta de emprego

TFS HealthScience is seeking a Site Coordinator to support a sponsor across the clinical development lifecycle. You will perform site study tasks, data entry, assist with SAE notifications, and help with patient recruitment and ethics submissions.

Based in Porto, Portugal, you will join our SRS/FSP team, travel as needed, and collaborate with investigators to maintain study quality and meet milestones.