Medical Director (Global Clinical Development)

Pentixapharm AG is a research-focused radiopharmaceutical and precision

oncology company with operations focused on the preclinical, clinical development

and manufacturing of the innovative theranostic drug peptide pair PentixaFor/

PentixaTher and antibody-based pipeline. The clinical stage drugs specifically

target the CXCR4 receptor, which is present in many rapidly progressing diseases,

including hematologic and solid cancers, as well as cardiovascular diseases.

The Medical Director (Global Clinical Development) will lead the global strategy

and execution of clinical trials in hematological and solid tumor indications, focusing

on radiopharmaceutical therapies. The role requires deep expertise in clinical

development and content leadership and hands on study execution in oncology.

You will collaborate with cross-functional teams to deliver innovative therapies to

market.

Tasks

• Lead global clinical development for novel radiopharmaceutical therapies

targeting hematological and solid tumors.

• Serve as the medical lead for oncology programs, guiding study design, writing

study protocols, reviewing patient data, clinical trial data interpretation

• Oversee clinical trials from first-in-human Phase I to Phase III, ensuring

compliance, on-time execution, and alignment with corporate goals.

• Manage clinical study portfolio, ensuring milestones are met and key endpoints,

such as ORR and PFS, are achieved.

• Prepare and participate in regulatory agency interactions for clinical

submissions, advice and approvals in Europe and the US.

• Mentor the clinical operational & development team, fostering collaboration and

scientific excellence.

• Stay informed on advancements in oncology and radiopharmaceuticals to guide

clinical strategies.

• Interact with Clinical Experts

Requirements

• MD or equivalent medical degree; Board certification / Specialization in

oncology preferred.

• 8+ years of experience in clinical development, including expertise in

hematological oncology, solid tumors, and radiopharmaceuticals.

• Proven track record of successful clinical trials, regulatory approvals and

leadership in global clinical programs.

• Strong knowledge of Phase I-III oncology clinical trial design and regulatory

requirements.

• Strong understanding of theranostic principals and radiopharmaceuticals

• Excellent communication, and interpersonal skills.

• Fluency in English; German proficiency is a plus.

Benefits

• Open-ended employment contract

• Flexible working hours and the opportunity to work partly from home

• A place of work on the innovative and sustainable Berlin-Buch Campus with

great offers such as a canteen, fitness center, campus bike & information

events

• Attractive company pension scheme options

• Company events such as company meetings, summer and Christmas parties

Ideas find their way with us! Thanks to our flat hierarchy and positive corporate culture, you can really

make a difference with us. We value our collegial working environment, which is characterized by mutual

respect, appreciation and varied and interesting activities.

If you are interested in this varied position, please send us your application by e-mail

to [email protected] stating your salary expectations and the earliest possible starting date.

Please use the subject line: "Medical Director" when submitting your application. If you have any

questions, please do not hesitate to contact us on +49 30 9489 2600.