We are looking for Clinical Project Manager

Jan 13, 2020


An exciting opportunity to dive in and begin your career with a company that have the ambition to be the leader in its domain. We will give you the mean to make your contribution highly impactful.

LNC Therapeutics is a French biotech company based in Bordeaux that develops microbiomebased therapies for impacting diseases. We have a pipeline of several projects at various stages of development, from early discovery to clinic. At LNC Therapeutics, we are committed to release the potential of the microbiome for patients with serious diseases by developing and delivering innovative human therapeutics. For this purpose, we harness live beneficial microorganisms inhabiting the gut to develop them as Live Biotherapeutics Products (LBPs) to treat complex diseases such as obesity and related metabolic disorders. LNC Therapeutics will continue to strengthen its pipeline through internal and external opportunities, aiming at becoming a leader at an international scale. 

Responsibilities include but are not limited to: 

  • Develop and manage Clinical project in an integrated way through detailed project schedules 
  • Delivery of trials according to company SOPs and ICH-GCP guideline with the support of CRO and CRU 
  • Support negotiation, decision-making and conflict resolution with external partners to achieve the objectives of the project and of the company 
  • Help the management team to make informed decisions 
  • Establish and manage collaborations  
  • Recruitment site monitoring
  • Manage and prioritize the support of several projects at the same time if necessary 
  • Communicate results effectively 
  • Write project reports including appropriate risk analysis and clear conclusions 
  • Write and contribute to writing grants and/or regulatory dossiers  
  • Regular travels to the US expected 


Education & professional experience 

  • Minimum Master 2 degree or equivalent in life sciences or related discipline; Ph.D. or Pharm. D preferred 
  • Minimum 3-4 years of clinical project management  
  • Experienced in management of clinical trials in compliance with FDA/EMA expectations  
  • Knowledge and understanding of FDA regulatory documentation 
  • Experience in CRO management 
  • Hands on experience in clinical monitoring, management of central and specialist laboratories, courier services, IMP management and quality management systems 
  • Experience and technical knowledge of vendor selection, monitoring and managing the delivery of vendor contracts to budget and timelines 
  • Professional experience in the biotechnology field 
  • Fluent in English (oral and written) 


Skills & Abilities 

  • Strong organizational skills, rigor and efficiency in the management of research programs in a timely manner and within budget 
  • Good relational skills 
  • Good scientific approach for data analysis 
  • Strong English communication capabilities – oral and written – for documents reporting, teleconferences, and oral presentations 
  • Dynamic, motivated, with a strong team spirit 


Location: Bordeaux, France

To apply for this opportunity, please send your resume and a cover letter to

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