Research Nurse

Planet Pharma; A distancia; EUR 30.000 - 50.000; A tiempo parcial

Descripción de la vacante

A global staffing agency is seeking experienced freelance Clinical Research Nurses in Spain for an Acute Ischaemic Stroke study. This role offers flexibility and requires conducting patient visits, performing clinical procedures, and managing documentation in compliance with protocols. Candidates should have a nursing qualification with a minimum of 3 years of experience, valid GCP certification, and the ability to travel. Join a dynamic team with the potential for increased work opportunities in clinical trials.

Formación

• Minimum of 3 years post-registration experience required.
• At least 1 year of acute clinical experience is essential.
• Previous clinical trial experience strongly preferred.
• All required immunisations must be up to date.
• Must have a valid GCP certificate.

Responsabilidades

• Conduct patient visits in line with study protocol.
• Perform clinical trial-related procedures including blood sampling and injections.
• Accurately document study activities in accordance with GCP.

Conocimientos

Venepuncture

Sample processing and centrifugation

Subcutaneous injection administration

Cannulation

ECG performance

Port-a-Cath access and de-access

Educación

Qualified nurse with a minimum of 3 years post-registration experience

Valid and current GCP certificate (R3)

Descripción del empleo

We are seeking experienced freelance Clinical Research Nurses to support an Acute Ischaemic Stroke study. This is an ad-hoc role with flexible scheduling, ideal for nurses currently working freelance or supporting multiple clients. Visits will be scheduled well in advance.

Lea atentamente toda la información sobre esta oportunidad y luego utilice el botón de solicitud de abajo para enviar su CV y su candidatura.

Study Overview

• Study Duration: 20 months
• Visit Duration: Approximately 2 hours per visit

Key Responsibilities

• Conduct patient visits in line with study protocol
• Perform clinical trial-related procedures including blood sampling and injections
• Process biological samples, including centrifugation
• Accurately document study activities in accordance with GCP and protocol requirements

Required Clinical Skills

• Venepuncture
• Sample processing and centrifugation
• Subcutaneous injection administration
• Cannulation
• ECG performance (recording only; interpretation not required)
• Port-a-Cath access and de-access

Essential Requirements

• Qualified nurse with a minimum of 3 years post-registration experience
• At least 1 year of acute clinical experience
• Previous clinical trial experience strongly preferred
• Valid and current GCP certificate (R3) — candidates in progress or planning to obtain soon will be considered (please confirm at submission)
• All required immunisations up to date
• Own car and willingness to travel to patient visits
• Flexible availability during weekdays

Additional Information

• This is an ad-hoc role; weekly or monthly hours are not guaranteed initially
• As additional studies are awarded, opportunities for increased work may become available
• Candidates must be comfortable working independently and managing schedules across multiple commitments

About Planet Pharma

Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head‑quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering.

Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing.

We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.