Senior Clinical Project Manager
vor 1 Woche
To keep our clinical study moving at Biotech speed, we need a dedicated, on-site
Senior Clinical Project Manager (Oncology)
to join our dynamic and growing team. In this pivotal role, you will be responsible for the planning, coordination, and oversight of our clinical Phase 2 oncology program. Key responsibility is to lead the clinical study team and to execute the clinical study within timelines, budget, and in compliance with regulatory and quality standards. The position is ideal for a Clinical Project Manager that wants to transform cancer care through innovative first-in-class therapies and work in a highly dynamic and driven science-based team.
Field of Responsibilities:
- Develop study protocols, schedules, study plans, and operational strategies.
- Manage and mentor cross-functional teams (clinical operations, medical monitoring, data management, regulatory, contract, and pharmacovigilance teams).
- Lead the planning, execution, and close-out of clinical trials, ensuring delivery on time, within budget, and to quality standards.
- Approve regulatory submission documents.
- Oversee patient recruitment, enrollment progress, and retention at each site.
- Review and assess trends in adverse events, safety signals, and protocol deviations.
- Approve site and vendor payments.
- Lead regular internal and external project meetings and report study status to leadership and stakeholders.
- Perform continuous risk assessments and implement mitigation plans.
- Review and contribute input to the company's internal and external presentations.
- Review and approve the company's clinical SOPs.
The Expertise You Bring
- Proven experience in early phase oncology trials as a CPM is required.
- Detail-oriented and data-driven, with a strong ability to analyse trial data, identify trends, and implement corrective actions as needed.
- Excellent communication and interpersonal skills, including the ability to resolve conflicts and find pragmatic solutions without breaking a sweat.
- Adaptability & mindset – thrives in a fast-paced environment, adaptable to change, and capable of handling complex situations
- Full‑time, on‑site presence in Munich to stay synced with lab and clinical teams.
Why Eisbach Bio
- High‑impact seat
: your planning and execution directly shape when patients gain access to first-in-class oncology therapies. - Flat hierarchy:
direct access to decision makers means no red tape when timelines shift or protocol changes are needed. - Agile cadence
: clear priorities, rapid decision-making, and biotech-level momentum keep your projects moving forward. - 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.
How to Apply:
To apply, please send your CV and an informative cover letter detailing your experience and suitability for the job to Please apply only by sending your application to the mentioned email address.
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.
Let's work together to pioneer groundbreaking therapies and deliver on the promise of our science.
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