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Clinical Study Assistant

Job in Palo Alto, Santa Clara County, California, 94306, USA
Listing for: Calculatrice
Full Time position
Listed on 2026-02-08
Job specializations:
  • Healthcare
    Clinical Research
Job Description & How to Apply Below

Overview

Clinical Study Assistant to support a clinical research project focused on voice recording and collection of personal and health-related data. The role involves recruiting participants across partner hospitals in Luxembourg, interacting with patients, visitors, and healthcare professionals, explaining study objectives and procedures, addressing questions, and supporting on-site inclusion workflows and follow-up visits. The assistant is part of the Clinical & Epidemiological Investigation Center (CIEC) at the Luxembourg Institute of Health (LIH) and will receive comprehensive training on the study protocol, tools, and communication guidelines.

Key

Accountabilities Participant Recruitment (Primary Mission)
  • Approach and inform potential participants (patients, visitors, healthcare staff) within hospital environments.
  • Clearly explain study objectives, procedures, and data protection aspects.
  • Assess eligibility and guide participants through the consent process.
  • Schedule and support voice recording sessions and related data collection.
  • Maintain a professional, empathetic, and patient-centered approach at all times.
  • Maintain participant retention throughout follow-ups.
Administrative & Operational Support
  • Ensure accurate documentation and data entry in study databases.
  • Maintain communication with clinical partners and the study coordination team.
  • Assist with logistical aspects (materials, tracking, scheduling).
  • Report recruitment progress and potential issues to the Nurse Lead.
Quality & Compliance
  • Follow Good Clinical Practice (GCP) principles after training.
  • Respect strict confidentiality and GDPR requirements.
  • Ensure protocol consistency and high-quality interactions with participants.
Key Skills, Experience and Qualifications
  • German or Portuguese: fluent or very good level
  • French and/or English: good working level
  • Luxembourgish: would be an asset
Interpersonal & Communication Skills
  • Strong interpersonal sensitivity and clear communication skills
  • Ability to engage effectively with individuals from diverse backgrounds and varying health situations
  • Comfortable interacting in busy hospital environments
  • Confident in approaching people and initiating conversations
  • Minimum requirement: secondary school diploma (baccalaureate or equivalent)
Candidate Profile
  • Candidates may come from various relevant domains, including but not limited to: healthcare support, social professions, research & clinical support, or any profile with strong communication skills and an interest in clinical research.
Personal Attributes
  • Patience and a strong ethical foundation
  • Ability to work autonomously while maintaining strong team spirit
  • Proactive and solution-oriented mindset
  • Rigorous, trustworthy, and highly respectful of confidentiality
What We Offer
  • A concrete role in an innovative research project in Luxembourg
  • Full training on study tools and communication guidelines
  • Supportive supervision by experienced clinical research staff
  • Opportunity to gain or reinforce experience in the field of clinical research
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