Clinical Data Manager (m/f/d)

Indivumed is a biotech company focusing on precision oncology. For almost 25 years we have been driven by a single overarching vision: a world in which precision therapy offers a cure for every cancer patient.
Our company is specialized in early drug discovery. Our R&D approach is based on our belief that we need to fundamentally understand the disease to gain novel insights and develop effective therapeutics. To do so we start with carefully collected and curated patient samples resulting in a comprehensive and proprietary database. By employing advanced biomathematical and bioinformatic methods on this excellent data we discover therapeutically novel targets. From our high-quality tissue we generate patient-derived 2D and 3D cellular models allowing us to perform target validation and therapeutic development in an environment that is as close to the patient as possible.

Drive dedication and our shared purpose make us who we are.

Driven by our pioneering spirit and our shared purpose we explore the complexity of cancer with curiosity and determination. Thriving on innovation we value unique perspectives and visionary scientific approaches to grow together . Whether as a scientist as a data analyst or in a corporate function everyone contributes to our common goal.

If you thrive on discovery come join our team and make your impact as

Clinical Data Manager (m/f/d)

Your responsibilites

We are looking for a highly organized and detail-driven Clinical Data Manager to lead data validation and quality oversight for
clinical data received from our global network including hospitals and academia.
This role is pivotal in ensuring that data collected across diverse clinical sites meets regulatory scientific and operational
standardssupporting our mission to deliver high-quality real-world clinical datasets for translational research and
other R&D activities.

• Coordinate and oversee data intake validation and quality control of clinical data submitted by partner hospitals worldwide.
• Review incoming datasets for accuracy completeness consistency and regulatory compliance (e.g. GCP GDPR).
• Collaborate with partner sites to clarify discrepancies resolve data issues and ensure alignment with protocol requirements and SOPs.
• Develop and maintain data validation rules data dictionaries and cross-site data consistency checks.
• Support and guide partners on data entry standards documentation formats and secure data transfer processes.
• Work closely with internal teams (clinical biobank bioinformatics R&D ITBD marketing) to ensure timely and reliable data integration.
• Monitor data flow timelines from partners and escalate risks or delays as needed.
• Assist in audit readiness by ensuring traceable documentation of all data validation activities.
• Contribute to the improvement of global data workflows and tools by identifying recurring data quality issues.

Our requirements

• Completed studies in biology or other life science (. . also welcome but not required)or medical training (MTA MFA OTA medical documentalist nurse)
• Experience with oncology biobank-linked data or longitudinal clinical data is a plus
• Strong Excel Skills (functions pivot-tables)
• Experience with database tools (e.g. MySQL) would be ideal but is not a must
• Proficiency in English German is a plus

Your benefits

• Demanding area of responsibility in a fast-growing company
• Grant for the HVV ProfiTicket/Deutschlandticket
• Subsidy for sports membership and events
• Company pension scheme
• Company doctor
• Fresh fruits and drinks
• Christmas and summer party
• Flexible working hours
• German and English courses
• 30 days holiday
• The 24th and 31st of December are holidays and wont be deducted from your annual holidays.

Would You Like to Contribute to the Success of Our Company

Please apply online and include your salary expectations and current notice period. Use our Apply now button here!