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Disclosure Lead (f/m/d)

Randstad Professionalmonheim, nordrhein westfalen🇩🇪GermanyPosted 12 Sept 2026

Why This Role Stands Out

This remote Disclosure Lead role offers significant career growth within the pharmaceutical industry, allowing you to develop expertise in global clinical trial transparency and regulatory compliance. You'll thrive here if you have a strong background in clinical research and a proactive, detail-oriented approach, supported by a flexible work environment and a competitive compensation package. Apply today to advance your career in a challenging and rewarding position!

Quick Overview

Seniority
Mid Senior
Employment type
Full Time
Work mode
Remote
Location
monheim, nordrhein westfalen, Germany
Clinical Research

Job Description

Do you want to progress professionally and desire a job where you are challenged and supported? With good benefits, diverse opportunities for further development, and the possibility to work mostly or fully remotely? Then you've come to the right place: Our subsidiary Randstad professional solutions offers an attractive position as clinical trial disclosure lead at a customer's location in Monheim . Apply online right away for this position in the pharmaceutical industry . We value equal opportunities and welcome applications from people with disabilities.

  • Define early disclosure strategies at study concept and protocol stages as well as during amendment stages
  • Prepare, review, and submit clinical trial registrations across global registries such as CTIS and ClinicalTrials.gov
  • Maintain accurate, up-to-date, and compliant registry records throughout the entire study lifecycle
  • Coordinate the creation and submission of clinical trial results disclosures
  • Ensure full inspection readiness through precise documentation and auditable evidence
  • Support data quality, system maintenance, and vendor oversight activities
  • Degree in Life Sciences or a related discipline 
  • Background in clinical research, trial management, Regulatory Affairs, or project management
  • Knowledge of clinical trial transparency and disclosure requirements
  • Familiarity with registries such as CTIS or ClinicalTrials.gov, and strong affinity for IT systems
  • Experience at a CRO or sponsor is a plus
  • Proficieny in spoken and written English; German language skills are a plus
  • Strong organizational skills and proactive communication style
  • High attention to detail and an open, collaborative mindset
  • Working time model: 37,5 h/week
  • Performance-based salary package depending on qualifications and professional experience
  • Up to 30 days vacation per year
  • Company pension scheme contribution after the end of the probationary period
  • Option of permanent employment with our business partner
  • A wide range of employee benefits/perks
  • Definition of career goals
  • Option for partial or full remote work

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