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Research data coordinator

Palermo
Contratto a tempo indeterminato
Apsida Life Science
Pubblicato il Pubblicato 20h fa
Descrizione

Job Title: Clinical Research Coordinator
Per candidarsi, è sufficiente leggere la seguente descrizione del lavoro e assicurarsi di allegare i documenti pertinenti.
Location: Palermo, Italy
Contract Type: Full-Time Contract (12 Months)
Overview
Apsida Life Science is currently partnering with a global clinical research organisation specialising in patient-focused trial support services and decentralised clinical trial solutions. The organisation is recognised for its strong international presence, operational flexibility, and commitment to improving patient access and clinical trial delivery across multiple therapeutic areas.
Key Responsibilities
Maintain and organize study files, regulatory documentation, laboratory kits, and study supplies.
Coordinate and manage ordering of laboratory kits and related clinical trial materials.
Prepare, package, and arrange shipment of biological samples in accordance with study and laboratory requirements.
Schedule subject visits, procedures, and assessments in collaboration with investigators and site staff.
Support patient visit coordination and ensure timely completion of study activities.
Complete electronic Case Report Forms (eCRFs) accurately and resolve data queries in a timely manner.
Assist in preparing the site for sponsor and CRO monitoring visits.
Ensure study documentation is maintained in compliance with GCP, protocol requirements, and site SOPs.
Support overall site operations and administrative clinical trial activities.
Requirements
Previous experience working as a Study Coordinator, Clinical Trial Coordinator, or similar clinical research role.
Intermediate level clinical research experience preferred.
Basic to intermediate English communication skills required.
Familiarity with eCRF completion and query resolution processes.
Experience handling study documentation, laboratory supplies, and sample shipments preferred.
Strong organizational and multitasking abilities.
Ability to work independently and collaboratively within a clinical research environment.
Knowledge of GCP and clinical trial processes preferred. xrdztoy
If you are interested in learning more, please reach out to KG Mphahlele at Apsida Life Science:

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