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Research Assistant - Barcelona

0-2 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) | Barcelona, Spain

Job Summary:
IQVIA is seeking a detail-oriented and proactive Research Assistant to join our clinical research team in Barcelona, Spain. This part-time, field-based role (24 hours per week) involves providing crucial administrative and operational support to ensure the smooth execution of clinical trials. Ideal for individuals with a background in life sciences or healthcare, this position offers a unique opportunity to contribute to cutting-edge research in a global pharmaceutical environment.


Key Responsibilities:

  • Support ongoing clinical research studies under the supervision of the Principal Investigator.

  • Maintain compliance with safety policies and study protocols.

  • Assist in maintaining study documentation including CRFs, EDC systems, and consent forms.

  • Coordinate logistics for study procedures and assist in clinical setup.

  • Label and inventory specimen collection tubes and manage study supplies.

  • Support data entry, data validation, and query resolution processes.

  • Assist in volunteer recruitment, screening, and orientation for studies.

  • Maintain proper custody and storage of study drugs per SOPs.

  • Collaborate with study monitors and respond to study queries promptly.


Required Skills & Qualifications:

  • BS/BA in Life Sciences or relevant clinical/medical field.

  • Prior experience in a clinical setting (e.g., clinical research coordinator, nurse, or medical assistant) preferred.

  • Basic understanding of clinical trial protocols and terminology.

  • Proficient in Microsoft Office (Access, Outlook, Excel, Word).

  • Strong interpersonal and organizational skills.

  • Attention to detail and ability to manage multiple administrative tasks.

  • Basic knowledge of EDC systems and data management procedures.


Perks & Benefits:

  • Opportunity to work with a global leader in healthcare research.

  • Exposure to international clinical trials and cutting-edge studies.

  • Collaborative, inclusive, and supportive work culture.

  • Flexible part-time schedule (24 hours/week).

  • Training and development opportunities within the IQVIA network.


Company Overview:

IQVIA is a world leader in advanced analytics, clinical research services, and healthcare data science, serving the life sciences and pharmaceutical industries. We power smarter healthcare with innovative research solutions that improve patient outcomes globally.


Work Mode: Field-based (On-site in Barcelona, Spain)


Ready to Join a Global Research Leader?

If you're passionate about clinical research and want to support world-class studies, apply now to start your career with IQVIA. Be part of our mission to improve global health through data and innovation.