Multispecific yet truly natural antibodies

Helping the body to fight cancer

Multispecific yet truly natural antibodies

Our biotechnology company researches, develops, and manufactures bispecific antibodies for the treatment of malignant tumors. We redirect the patient´s own immune cells, especially macrophages, T-cells and natural killer cells, to attack cancer cells – helping the body to fight cancer
Who we are
Who we are

Long-term pharma experience meets academia

Our antibody development roots go deep

Our focus
Our focus

Multispecific yet natural

Helping the body to fight cancer

CD47 Dual targeting
Our Pipeline

Fully human bispecific antibodies for cancer treatment

Safe and selective blockade of CD47 on tumors

Looking into the future
Partner with us

Interested in working with LamKap Bio?

Beyond bispecific antibodies

previous arrow
next arrow

Light Chain Bioscience (LCB), a brand of Novimmune SA, is a drug discovery and development company located in Geneva, Switzerland. To date, Novimmune has generated seven therapeutic antibodies, successfully bringing one to approval for an orphan indication in children. The focus is now on the generation of fully human bispecific antibodies using a proprietary technology platform.

LCB is seeking a Clinical Project Manager to bring a bispecific antibody program currently at the pre-IND/CTA stage into Phase I clinical development.

Key Responsibilities:

  • Coordinate late-stage preclinical, regulatory & manufacturing activities to support IND/CTA submission (outsourcing, budget and timelines)
  • Manage clinical CRO selection and clinical trial set up in accordance with company’s Standard Operating Procedures
  • Responsible for the operational management of clinical study, ensuring compliance with timelines, milestones and budget
  • Act as the main line of communication to relevant stakeholders and provide input to feasibility, study design, budget development and ensure regular progress reporting (resources, budget and timelines)
  • Provide input on study related documents (e.g. IB, IMPD, ICF, CRF, Protocol, Lab. Manual etc.)

Profile:

  • Degree in health care, life sciences or related field
  • Minimum of 5 years of experience in clinical research
  • Knowledge of clinical trial design and development
  • Experience with coordinating a team Knowledge of early phase oncology trials a plus
  • Fluency in English required

Interested applicants should send their CV and motivation letter, in English to This email address is being protected from spambots. You need JavaScript enabled to view it.