Manager, Preclinical Development at Immunic Therapeutics

Gräfelfing, Bavaria, Germany -

Full Time

Start Date

Immediate

Expiry Date

10 Sep, 26

Salary

0.0

Posted On

12 Jun, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Preclinical Development, CRO Management, Toxicology, Pharmacokinetics, ADME, GLP Guidelines, ICH Guidelines, Bioanalytics, LC-MS/MS, Toxikinetics, Project Management, Regulatory Compliance

Industry

Biotechnology Research

Description

Your mission We are seeking a motivated and hands-on Manager, Preclinical Development to drive the execution of our preclinical development activities and contribute to the advancement of our innovative drug development programs. In this role, you will coordinate and oversee preclinical studies with external partners, ensuring high-quality execution in line with regulatory standards and project timelines. You will work closely with cross-functional teams and play a key role in advancing innovative therapies from research into development. Key Responsibilities: Manage and strengthen collaborations with CROs and external experts, including coordination of proposals, CDAs , contracts and invoice. Plan, monitor, and evaluate preclinical in vitro and in vivo studies in compliance with ICH and GLP guidelines. Oversee studies across toxicology, safety, pharmacokinetics and ADME. Review study protocols, data, reports, and relevant regulatory and program documents (e.g. IB, Safety Data Sheets). Ensure timely execution and high-quality delivery of studies conducted by external partners. Act as the preclinical study representative within cross-functional program and study teams. Communicate effectively with internal and external stakeholders and represent preclinical topics in meetings. Your profile Advanced degree (MSc, PhD) in pharmaceutical sciences, biology, chemistry or a related field. 3-5+ years of relevant experience in preclinical development, preferably within biotech, pharma or CRO environment. Strong scientific expertise in DMPK, safety and toxicology, ideally with experience in bioanalytics (e.g. LC-MS/MS) and toxikinetics. Proven record in managing outsourced studies and effectively collaborating with external partners. Ability to drive projects independently, take ownership and manage multiple priorities reliably. Structured, detail-oriented working style with strong organizational skills. Collaborative mindset with a proactive, solution-oriented approach and team player attitude. Excellent English skills. Why us? A permanent full-time position in an international and highly motivated team. A dynamic, flexible and innovative working environment. Participation in our company’s success through our stock option program. Competitive compensation, comprehensive benefits and opportunities for professional growth. Further benefits that promote our employee’s health and wellbeing: Wellpass, OpenUp, and more. About us Immunic Therapeutics is a dynamic biotechnology company with a pipeline of selective, orally available immunology therapies for the treatment of chronic inflammatory and autoimmune diseases. Currently, three small molecule product candidates are in various stages of clinical development. For more information, please visit: www.imux.com.

Responsibilities

The role involves coordinating and overseeing preclinical in vitro and in vivo studies with external partners and CROs. The manager will ensure high-quality execution of toxicology, safety, and pharmacokinetics studies in compliance with regulatory standards.