Director, Global Medical Affairs -Publications (f/m/d)
Lead the development, execution, and continuous optimization of the annual publication plan for pipeline and marketed products
Develop scientific publications, including abstracts, posters, oral presentations, and manuscripts for submission to peer‑reviewed journals
Coordinate and manage internal and external publication review and approval processes
Collaborate cross‑functionally with Clinical Research, Biostatistics, Regulatory Affairs, Dosimetry, and Global Medical Affairs teams
Ensure scientific accuracy, regulatory compliance, and adherence to FDA regulations, ICH guidelines, and journal requirements
Oversee disclosure management, conflict of interest documentation, and quality reviews of all publication materials
Manage journal submission workflows, publication tracking systems, timelines, and coordination with external investigators, agencies, and scientific conferences
Oversee budgets, timelines, and vendor management while adapting publication strategies based on emerging clinical data, trial milestones, and regulatory updates
Your profile
Advanced degree required: MD, PharmD, or PhD in Oncology, Nuclear Medicine, or a related scientific discipline
7‑10 years of experience leading publications within Medical Affairs, preferably in oncology, radiopharmaceuticals, or specialty therapeutics
Extensive experience in publication management, medical writing, and clinical trial publications within the biotech or pharmaceutical industry
In‑depth knowledge of GCP, ICH guidelines, medical compliance standards, and scientific dissemination strategies
Strong project management and organizational skills with the ability to manage multiple concurrent publications, priorities, and deadlines in a dynamic environment
Proven ability to work effectively in cross‑functional and matrixed organizations, collaborating with internal stakeholders, external experts, and key opinion leaders
Exceptional scientific writing, editing, communication, and presentation skills, as well as strong English language proficiency
Our offer
Exciting challenges in an up‑and‑coming and fast‑growing company with a high degree of creative freedom
An open working atmosphere in an international corporate culture with short communication channels
Flexible working hours with home office options
Attractive special payments
Just a good salary? Not with us! We also offer you
Employee participation programme
Job bike or subsidised job ticket
Above‑average contribution to the company pension scheme
Individually tailored further training programme (including German and English courses)
Health promotion programmes (e.g. EGYM Wellpass, subsidy for local fitness studio, sponsorship of sporting events, various lifestyle coaching sessions)
ITM is an employer that ensures equal opportunities. Qualified applicants are encouraged to apply and will be considered during the selection process regardless of gender, age, national or ethnic origin, religion or belief, disability, sexual orientation, gender identity, or any other characteristic protected under the German General Equal Treatment Act (AGG).
We also accept reasonable accommodations for applicants with disabilities. Please contact career@itm-radiopharma.com if you require an accommodation.
#J-18808-Ljbffr