Clinical Research Coordinator
Are you seeking an opportunity in Clinical Research? Do you want to work for an industry-leading company? If so, join us - IQVIA is looking for a Clinical Research Coordinator.
This part-time role (24 hours) supports a site in Belfast conducting a clinical trial in the respiratory field.
As a key member of the site team, you will handle various administrative tasks to support investigators, ensure smooth clinical trial operations, and assist with patient data collection.
Day-to-day responsibilities include:
* Supporting clinical research studies and maintaining a safe environment per health and safety policies under the guidance of the Principal Investigator.
* Safeguarding participant well-being, acting as a volunteer advocate, and addressing concerns.
* Keeping study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other documents current.
* Planning and coordinating logistics for study procedures per protocol.
* Preparing for studies, including labeling specimens, inventory management, and troubleshooting equipment.
* Assisting with data entry, quality checks, and resolving queries to ensure protocol adherence and data accuracy.
* Supporting study enrollment through recruitment, screening, and participant orientation.
* Managing study drug custody following standard procedures.
* Collaborating with study monitors and responding to their questions effectively.
Qualifications and skills required:
* BSc/BA in life sciences or equivalent, or relevant clinical experience (e.g., research coordinator, nurse, medical assistant).
* Basic understanding of clinical trials, protocols, consent forms, and schedules.
* Knowledge of medical terminology.
* Proficiency with MS Windows and Office, including Access, Outlook, Excel, Word.
* Excellent interpersonal skills for effective teamwork and communication.
* Strong organizational skills with attention to detail.
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