Data Transparency Specialist – Data Sharing, Anonymisation and Clinical Trial Disclosure (f / m[...]

Staburo GmbH; München; Hybrid; EUR 45.000 - 65.000; Vollzeit

Zusammenfassung

A data science company in Munich is seeking a professional to handle the redaction of clinical trial documents and manage submission processes. The ideal candidate will have a degree in data science or life science, alongside skills in data anonymization and knowledge of regulatory policies. This role offers flexible working hours and the possibility of remote work options.

Leistungen

Flexible working hours

Subsidised canteen

Opportunity to work from home

Qualifikationen

• 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 medical writing is a plus.

Aufgaben

• Redaction of clinical trial documents and anonymisation of individual patient data.
• Preparing redaction proposal document packages for EMA Policy 0070.
• Communicate and coordinate with international study teams.

Kenntnisse

Data anonymization

Analytical thinking

Teamwork

Excellent organizational skills

Good English skills

Ausbildung

University degree in data science or life science

Tools

R

SAS

Jobbeschreibung

Your responsibilities will include

• Redaction of clinical trial documents and anonymisation of individual patient data
• Preparing redaction proposal document packages for EMA Policy 0070 and Health Canada PRCI submissions
• Assessing data sharing requests, reviewing informed consent forms for data sharing feasibility
• Disclosure activities for drug and device clinical trial information :
• Authoring of protocol registrations and results postings 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 lifescience 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, German is an advantage

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 [e-mail] .

About us

Staburo GmbH is a data science company, specialized in statistical consulting, programming and bioinformatics for healthcare projects. Our core competencies include Clinical Statistics, Translational Medicine & Biomarkers, Phase I & Pharmacokinetics / -Dynamics, Data Transparency & Disclosure Services, Health Technology Assessment and Bioinformatics. Our customers are international pharmaceutical companies, CROs, biotech companies and medical device manufacturers. Our steadily growing team supports our clients efficiently from study design to data analysis and finally the disclosing and posting of trial results.