Study Coordinator

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

About This Role

TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full-service capabilities, resourcing, and Functional Service (FSP) solutions.

The Site Coordinator is responsible for performing assigned Site Study tasks, working to facilitate the Principal Investigator (PI) job, contributing to the quality of the study, providing appropriate support to reach the milestones, pro-actively recruiting new patients and speeding up any data-entry process.

As part of our SRS/FSP team, you will be dedicated to one sponsor, a global pharmaceutical or biotechnology company that is an industry leader within its therapeutic area.

Key Responsibilities

• 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.

Qualifications

• Bachelor’s Degree, preferably in life science or proven experienced in the role, only applicable when exclusively data entry tasks are going to be developed by the TFS’ 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.

What We Offer

We provide opportunities for personal and professional growth in a rewarding environment. You will join a team that values collaboration, quality, and making a difference in the lives of patients.

Our core values of Trust, Quality, Passion, Flexibility, and Sustainability guide our decisions and shape our culture. By aligning on these values, we foster collaboration, innovation, and a shared commitment to excellence. Together, we make a difference.

A Bit More About Us

Our journey began over 30 years ago in Sweden, in the city of Lund. As a full-service global CRO, we build solution-driven teams working toward a healthier future. Bringing together over 600 professionals, TFS delivers tailored clinical research services in more than 50 countries, offering flexible clinical development and strategic resourcing solutions across key therapeutic areas including Dermatology, Neuroscience, Oncology, and Ophthalmology.

TFS HealthScience

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.