Data Transparency Specialist – Data Sharing, Anonymisation and Clinical Trial Disclosure (f/m/d - part/full-time)

Staburo GmbH

Source: PersonioLocation: EU/EMEAConfirmed active: Sep 11, 2026
Full-timePart-timeHealthcare

Key points from the posting

Tech stack
RSASClinicalTrials.govEudraCTCTISEMA Policy 0070Health Canada PRCIRPDPCCIPPD
Benefits
  • Flexible working hours
  • Comprehensive individual development opportunities
  • Continuous trainings
  • Subsidised canteen
  • Interdisciplinary team
Languages:
English

Read out of the job posting automatically

Our assessment

  • Our reading of the full posting text confirms it: fully remote.
  • 3 more open roles from this employer in our index. 3 of them fully remote.

This section only: calculated automatically by nomado24, from our own job index and our own reading of the posting text. Not stated by the employer.

Job description

Your responsibilities will include

  • Assessing data sharing requests, reviewing informed consent forms for data sharing feasibility
  • Redaction of clinical trial documents and anonymisation of individual patient data
  • Preparing Redaction Proposal Document Packages (RPDP) for submission to EMA and Health Canada in compliance with EMA Policy 0070 and Health Canada PRCI
  • Disclosure of clinical trial information for drugs and medical devices: Registering protocols and preparing results for submission to local and global regulatory agencies
  • Maintenance of study records including status tracking and administrative aspects
  • Managing timelines for timely submission to ensure compliance with international laws, regulations, and guidelines
  • Communicate and coordinate with international study teams, act as a central point of contact

Your profile

  • University degree in data science or life science related discipline
  • Knowledge of drug development and clinical science
  • Experience in redaction of CCI and PPD in clinical documents is a plus
  • Knowledge of EMA policy 0070 and Health Canada PRCI is a plus
  • Experience in data anonymization and programming (e.g., R/SAS) is a plus
  • Knowledge of the clinical trials disclosure regulatory environment and experience with Clinicaltrials.gov and EudraCT/CTIS is a plus
  • Experience in medical writing is a plus
  • Fast comprehension, analytical thinking, teamwork and a high degree of initiative, willingness to learn
  • Work experience in a CRO or pharma/biotech is a plus
  • Excellent organizational and time management skills, highly detail-oriented
  • Good English skills

What we offer you

We value communication, flat hierarchies, open corporate culture, and a harmonious work environment. We offer comprehensive individual development opportunities, continuous trainings, and flexible working hours. A modern and bright office with a subsidised canteen, as well as the opportunity to work 2 days per week from home are part of our everyday working life. Full remote work from anywhere in Germany for those who do not live in Munich can be discussed. You will join an interdisciplinary team allowing you to discuss with and learn from peers with many different backgrounds.

Question?

If you have any questions, please feel free to contact us by e-mail  application@staburo.de .

Biostatistics and Data SciencePermanent Employeepermanentfull or part time

This role is provided by an external source. Applications are handled on the source website.

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