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Research Assistant

0-3 years
Not Disclosed
10 June 25, 2025
Job Description
Job Type: Part Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Research Assistant – Clinical Trials (Part-Time, Field-Based) – Valencia, Spain

Location: Valencia, Spain
Job Type: Part-Time
Work Mode: Field-Based
Company: IQVIA


Job Summary

IQVIA, a global leader in healthcare intelligence and clinical research, is hiring a Research Assistant for a part-time, field-based position in Valencia. This is an excellent opportunity for candidates with a background in clinical environments, life sciences, or medical assistance who want to support the smooth execution of clinical trials. You will play a crucial role in administrative and patient data support, ensuring protocol compliance and contributing to high-quality research outcomes.


Key Responsibilities

  • Support clinical research studies under the direction of the Principal Investigator.

  • Maintain up-to-date study protocols, CRFs, and EDC systems.

  • Assist in study planning and logistics including equipment setup and inventory.

  • Aid with data entry, query resolution, and data quality control.

  • Perform patient recruitment, screening, and orientation as per protocol.

  • Ensure proper custody and documentation of study drug per SOP.

  • Respond to study monitor queries and coordinate on-site activities.

  • Ensure adherence to health and safety policies and promote subject well-being.


Required Skills & Qualifications

  • Bachelor’s degree in life sciences or relevant clinical/medical experience (e.g., nurse, clinical coordinator).

  • Basic knowledge of clinical trial protocols and regulatory documentation.

  • Familiarity with clinical research procedures, EDC systems, and CRFs.

  • Basic understanding of medical terminology.

  • Strong IT skills – proficiency in Microsoft Excel, Word, Outlook, and Access.

  • Excellent interpersonal and communication abilities.

  • High attention to detail and strong organizational skills.


Perks & Benefits

  • Part-time flexibility in a leading global organization

  • Experience in real-world clinical trial execution

  • Exposure to international study protocols and global health research

  • Career growth and training in clinical research practices


Company Description

IQVIA is a top global provider of advanced clinical research, real-world evidence solutions, and healthcare data analytics. At the forefront of innovation in life sciences, IQVIA accelerates the development and commercialization of modern medical treatments to enhance global health outcomes.


Work Mode

Field-Based (Valencia, Spain)


Take the Next Step in Your Research Career

If you're looking to build your experience in clinical research and contribute to meaningful healthcare innovation, apply now for the Research Assistant role at IQVIA.