Clinical Research Nurse

About the Role

[Employer hidden] is a leading global mid size Contract Research Organization partnering with pharmaceutical and biotechnology companies across the full clinical development lifecycle. We deliver flexible full service, resourcing and Functional Service Partnership solutions tailored to our clients’ needs.

The Clinical Research Nurse is responsible for supporting the execution of clinical trials at site level, ensuring high quality patient care and protocol compliant clinical activities, including both on site and decentralised visits such as home visits where required.

This position may be offered as either a permanent full time role or a freelance engagement, depending on local market conditions, availability and study needs.

As part of our SRS or FSP delivery model, you will be fully dedicated to one sponsor, working closely with a global pharmaceutical or biotechnology company that is a leader within its therapeutic area.

Key Responsibilities

• Perform protocol specified clinical trial activities, including patient visits, clinical assessments and data collection
• Administer investigational medicinal products in accordance with protocol, GCP and local regulations
• Conduct home visits and support decentralised trial activities when required
• Collect and document vital signs and other protocol specific clinical assessments
• Ensure accurate and timely documentation in trial systems and source records
• Maintain a high standard of patient care, acting as a key point of contact for study participants
• Collaborate closely with investigators, site staff and sponsor teams to support trial delivery
• Comply with all local hospital credentialing and site requirements

Qualifications

• Registered Nurse qualification, valid in the country of practice
• Current GCP certification
• Previous experience working in clinical trials or clinical research
• Experience with IMP administration and patient facing clinical activities
• Ability and willingness to travel domestically, including for home visits if required
• Strong communication skills and a patient focused mindset
• Fluency in the local language, both written and spoken

What We Offer

We offer a flexible working model with opportunities for both permanent employment and freelance collaboration, depending on individual preference and study requirements.

You will be part of an international and supportive organization that values quality, collaboration and continuous improvement. At TFS, we are committed to creating an environment where professionals can grow, contribute and make a meaningful impact on patients’ lives.

Our core values of Trust, Quality, Passion, Flexibility and Sustainability guide how we work and how we partner with our clients. By living these values, we build strong relationships and deliver high quality clinical research together.

A Bit More About Us

Founded over 30 years ago in Lund, Sweden, [Employer hidden] has grown into a global CRO with more than 600 professionals supporting clinical research in over 50 countries. We build solution driven teams focused on delivering efficient, patient centric clinical development across multiple therapeutic areas including Dermatology, Neuroscience, Oncology and Ophthalmology.