Clinical Research Coordinator (Ad-hoc/Part-time)

Position: Clinical Research Coordinator (Ad-hoc/Part-time)

Location: Remote in Spain

Client: CRO

Type: Ad-hoc - Must be Freelancer

Main Responsibilities

• Coordinate the end-to-end setup, delivery, and management of home-based clinical trial projects.
• Support and train Clinical Research Nurses on study protocols and procedures.
• Act as the key liaison between study sites, CROs, sponsors, and nursing teams.
• Manage project logistics, including nurse allocation, sample shipments, and equipment delivery.
• Monitor project progress, identify risks/issues, and ensure compliance with GCP, SOPs, and regulatory requirements.
• Support audits and ensure accurate reporting of study activities, incidents, and safety events.

Main Requirements

• Previous experience as a Clinical Research Coordinator (CRC), ideally with a nursing background.
• Strong knowledge of clinical trial regulations and ICH-GCP guidelines.
• Experience working with clinical trial sites, CROs, and sponsors.
• Proven project coordination and operational management skills within clinical research.
• Registered Nurse (NMC) or equivalent nursing qualification preferred.
• Must be set up as Freelancer

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.

www.planet-pharma.com