Clinical Scientist*

Eintrag vom 09.03.2026

Professional Focus

• Perform critical scientific and statistical interpretation of clinical data, providing clear insights to support sound, evidence-based decision-making.
• Contribute to the planning, execution, and interpretation of pre-planned, exploratory, and post-hoc analyses, ensuring scientific rigor, transparency, and appropriate contextualization of results.
• Contribute to protocol and protocol amendment development, including review of eligibility criteria, endpoints, and assessments.
• Review and provide scientific input on clinical data–related documents, including statistical analysis plans (SAPs), tables, listings, and figures (TLFs), and clinical study reports (CSRs).
• Effectively communicate clinical data and scientific conclusions, both orally and through high-quality presentations, to internal and external stakeholders.
• Support the preparation, review, and scientific alignment of regulatory and scientific documentation, such as briefing documents and responses to health authority questions. Actively contribute to clinical development strategy, including benefit–risk assessments, study optimization, interpretation of emerging data, and program-level decision-making processes.
• Provide scientific guidance on clinical study design, including definition of study objectives, endpoints, eligibility criteria, and key statistical considerations, in close collaboration with the Clinical Operations team.
• Collaborate effectively in a cross-functional, matrix environment with Clinical Operations, Biostatistics, Regulatory Affairs, Medical Writing, and external partners to ensure scientific alignment and high-quality execution.
• Support the development of abstracts, posters, and manuscripts for submission to peer-reviewed journals and scientific congresses, in collaboration with Medical Writing and Publications teams.

Your Building Blocks for Joint Success

• Advanced degree in life sciences or a related discipline (MD, PhD, PharmD or equivalent).
• Strong expertise in clinical development, data interpretation and biostatistics with the ability to critically assess analyses, assumptions, and conclusions.
• Proven ability to interpret complex datasets and derive scientifically robust conclusions.
• Demonstrated strength in scientific communication, including clear oral presentations and the development of high-quality scientific slide decks for internal and external audiences.
• Extensive scientific writing experience, including authorship or substantial contribution to peer reviewed publications.
• Solid understanding of clinical trial methodology, Good Clinical Practice (GCP), and regulatory requirements across the clinical development lifecycle.
• Strong ability to collaborate in a cross functional, matrix organization (Clinical Operations, Biostatistics, Regulatory Affairs, Medical Writing).
• High level of scientific rigor, attention to detail, and commitment to data integrity.
• Proven capability to work independently while contributing effectively within cross functional teams.
• Excellent English communication skills, both written and verbal.

What We Offer

• Full-time permanent position with attractive compensation
• A motivated, supportive, and collaborative team
• Opportunity to work with leading experts in clinical development, regenerative medicine, and ATMPs
• Collaborative and international working environment with strong scientific exchange
• Diverse training and professional development opportunities
• Flexible, individual mobility budget as well as free parking
• Complimentary beverages and fresh fruit for the workday
• Extensive corporate benefits
• Company pension scheme

Does this sound like a work culture that suits you?

Then we look forward to getting to know you! Please send your complete application documents (cover letter, CV, certificates) stating your salary expectations and earliest possible starting date:

Personaldienstleister bitten wir, von Vermittlungsangeboten abzusehen. Vielen Dank!

*Die Verwendung der männlichen Sprachform dient alleine der besseren Lesbarkeit, umfasst aber die Angehörigen aller Geschlechter

**Pflichtfeld

Datenschutz:
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