Multispecific yet truly natural antibodies

Taking next generation, multispecific antibody technologies into Alzheimer’s Disease and Antimicrobial Resistance

Taking next generation, multispecific antibody technologies into Alzheimer’s Disease and Antimicrobial Resistance

Who we are
Who we are

Long term pharma and biotech professionals with a track record of leading projects from research into the market

Our antibody development roots go deep

Our focus
Our focus

Multispecific yet natural

Alzheimer’s Disease and Antimicrobial Resistance

CD47 Dual targeting
Our pipeline

Fully human bi- and multi-specific antibodies for the treatment of Alzheimer’s Disease and Antimicrobial Resistant infections

Safe and selective blockade of CD47 on tumors

Looking into the future
Looking into the future

Beyond bispecific antibodies

Beyond bispecific antibodies

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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 Diese E-Mail-Adresse ist vor Spambots geschützt! Zur Anzeige muss JavaScript eingeschaltet sein.