Pharmacist (m/w/d)

As a medium-sized company based in Ladenburg near Heidelberg, we place great importance on an open and collegial work environment. We address each other informally, enjoy working as a team, and take responsibility for our areas of work. Together, we are developing a new treatment approach in oncology. Based on our ADC technologies, we are developing novel drugs for targeted and highly effective cancer treatment. ADCs are antibody-drug conjugates that combine the specificity of antibodies with the potency of toxins to specifically target cancer cells. We use multiple payloads and have built an ADC toolbox that overcomes tumor resistance through diverse mechanisms and targets different types of cancer via various antibodies. Our goal is to develop targeted and highly effective ADCs for the treatment of a wide range of malignant hematological and solid tumors.

We offer diverse positions in research, development, and administration. We support you on your personal career path and offer you a wide range of opportunities for professional development.

We welcome all applications regardless of origin, gender, age, physical characteristics, disability, religion, personal orientation, gender identity, or any other criterion under applicable law. What matters to us are your strengths and experience. We promote diversity and equal opportunity by treating all applications fairly and avoiding discrimination.

We are looking to hire a

Clinical Scientist (f/m/d)

To strengthen our Clinical Team at our Ladenburg site, we are hiring a full-time, permanent Clinical Scientist to join us at the earliest possible date. This role is ideal for someone who enjoys working hands-on with clinical data and taking scientific ownership across our clinical development programs.

This is a hybrid position requiring 2-3 days per week on site in Ladenburg.

You provide medical and scientific input for successful planning, execution, analysis, and reporting of clinical trials, including contributions to clinical study protocols, protocol amendments, investigator brochure updates, and Clinical Study Reports.

You serve as the day-to-day scientific and clinical contact for investigational sites, CROs, vendors, and external partners, ensuring high-quality scientific exchange and timely issue resolution

You will review, interpret, and present clinical trial data, deriving scientific insights to support evidence-based decision-making, benefit-risk assessments, and trial optimization

You will conduct in-depth research on clinical, scientific, and competitive topics to inform clinical development strategy, trial design, data analysis, and scientific publications

You will collaborate closely with Regulatory Affairs, Clinical Operations, Biostatistics, Translational Research, Manufacturing, and external partners to support the timely delivery of high-quality clinical data and robust clinical development outputs

You have a Master's degree or PhD in Life Sciences, Pharmacy, Medicine, or a related field (e.g. Biochemistry, Biology, Pharmacology)

You have at least 5 years of hands-on industry experience in clinical development as Clinical Scientist within CROs, Pharmaceutical or Biotechnology Industry environment; oncology or hematology background is a plus

You have natural passion for clinical study data - you enjoy exploring, questioning, and turning data into insight

You are a highly motivated, self-dependent, problem solver and have a proactive personality with the ability to work in a multi-cultural, cross-functional team

You uphold patient safety, data integrity, and data protection and confidentiality to the highest standard. Solid knowledge of clinical research standards (ICH-GCP, clinical trial methodology, regulatory expectations) is required

You are fluent in business and medical English complete your profile. German language skills would be an advantage

Flexible working hours with compensation options and the opportunity to work remotely so that...