Responsibilities
Provide medical oversight across studies, input into clinical trials design and protocol
Act a senior medical lead for safety review, clinical data interpretation and investigator engagement
Hands on processing of AEs and SAEs, including case intake, medical review, causality assessment, and follow up
Preparation and submission of SUSARs, DSURs, safety narratives, and line listings
Daily safety data review and reconciliation with clinical and data management
Active participation in Safety Review Committees
Drafting, implementation, and continuous improvement of pharmacovigilance SOPs and workflows
Close collaboration with vendors and clinical sites on safety and medical topics
Maintenance of safety documentation and readiness for audits and inspections
Ensuring compliance with GVP, ICH GCP, and regulatory requirements
Supporting safety sections of protocols, IBs, and other clinical study documents
Hands on support across teams when needed, contributing your expertise beyond pharmacovigilance in a collaborative startup environment where everyone helps to get things done
Your Expertise
University degree in human medicine
Medical doctor with specialization in oncology
Experienced in clinical oncology trials, in pharmacovigilance and clinical drug safety, ideally in a biotech or CRO setting
Previous experience in pharmacovigilance systems and safety data base is a plus
Strong understanding of clinical trial safety processes and regulatory requirements
Comfortable working independently and taking responsibility in a small team
Structured, reliable, and detail-oriented working style
Willingness to work fully on site and be an active part of the local team
Very good English skills
Why Eisbach
High impact seat: your turnaround times decide when patients receive first in class medicines.
Flat hierarchy: direct access to decision makers means zero red tape when a clause needs approval.
Agile cadence: clear priorities, instant feedback loops, biotech level momentum.
Vibrant workspace: labs and offices in the heart of Munich’s biotech hub, plus barista‑grade coffee and regular science socials.
We offer a competitive salary, comprehensive benefits and a Stock Option Plan that allows you to share in the long-term success and growth of our transformative company.
If you are a driven, committed, inventive and resilient professional looking to make a real impact for the benefit of our patients, we love to hear from you.
To apply, please submit your CV and an informative cover letter detailing your experience and suitability for the job.
We deliver on the promise of our cutting-edge science to pioneer new drugs. Together, we pledge to transform the lives of patients and be good stewards of our community.
How will you apply your curiosity? Tell us at: careers@eisbach.bio
Please note that we are seeking passionate individuals who want to engage directly with us, without intermediaries or recruiters.
Eisbach Bio embraces diversity and is committed to equal opportunity for all employees and applicants.