Job Title: Director of Clinical Operations
Location: Germany (Hybrid/Flexible Work Options Available)
Employment Type: Full-Time, Permanent
About Us:
We are a fast-growing oncology-focused biotechnology company pioneering novel therapeutics to address high unmet medical needs in cancer. With a pipeline built on cutting-edge science and a patient-first mindset, we are expanding our clinical operations team to support our next phase of growth. Our mission is to transform the lives of cancer patients through breakthrough innovation—and we’re looking for bold and visionary leaders to help drive that mission forward.
Position Summary:
As Director of Clinical Operations, you will lead the strategic planning, execution, and delivery of our clinical development programs across all phases. Reporting directly to the VP of Clinical Development, you will be responsible for building and managing a high-performing team, overseeing CRO and vendor relationships, ensuring GCP compliance, and delivering clinical trials on time and within budget. This is a high-impact role with significant visibility and influence on the company’s success.
Key Responsibilities:
* Lead and manage all operational aspects of clinical trials from initiation through close-out.
* Develop and execute clinical development operational strategies in alignment with corporate objectives.
* Select, oversee, and manage CROs, vendors, and consultants to ensure timely and quality trial execution.
* Build and lead a growing team of clinical operations professionals in Germany and across Europe.
* Ensure full compliance with ICH-GCP, EMA, and other regulatory requirements.
* Oversee budget planning, forecasting, and management for clinical programs.
* Serve as a key point of contact for cross-functional teams including Regulatory Affairs, Medical, CMC, and Quality.
* Represent Clinical Operations at internal leadership meetings, Board updates, and regulatory agency interactions as needed.
Requirements:
* Advanced degree in life sciences (e.g., MSc, PhD, PharmD, or MD preferred).
* Minimum of 10 years of experience in clinical research with at least 5 years in oncology and 3+ years in a leadership role.
* Proven track record in managing global clinical trials, preferably in early- to mid-stage biotech environments.
* Strong knowledge of GCP, EMA/FDA regulations, and clinical trial design.
* Experience with vendor and budget management, risk mitigation, and regulatory submissions.
* Fluency in English (German is a plus but not required).
* Based in Germany or willing to relocate; flexible work arrangements available.
1. What We Offer:
* Competitive compensation package including equity options.
* Opportunity to work with a visionary team making a real impact in cancer care.
* Collaborative, science-driven culture with a commitment to professional development.
* Hybrid working model with flexibility to balance office and remote work.