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Senior Project Manager: Therapeutic drug development

ABG-92113 Emploi Sénior
18/05/2020 CDI Salaire à négocier
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Leads To Development
Paris - Ile-de-France - France
project management, regulatory affairs, Non-clinical drug development
Recherche et Développement


Leads to Development provides specialist expertise on the preclinical and non-clinical development of medicinal products to the biotechnology and pharmaceutical industry.

As an internationally renowned consultancy and services company, based in Paris, L2D provides hands-on management of the preclinical development of its clients’ new drug programmes advancing them from the bench to the clinic.

Covering a wide variety of product types and indications for clients across Europe and the US, we use a team approach to provide strategic and regulatory advice, write development plans, and undertake project management. We also write key regulatory documents to support the products’ clinical trial applications.

For the last 11 years we have surpassed the expectations of our biotech and mid-sized pharmaceutical clients by delivering increased product development efficiency, minimised project risk and added product value.

To sustain our current strong development phase, we are recruiting a senior project manager.

Poste et missions

Team leadership and project management of the preclinical development of medicinal products including the writing of regulatory documents

As a Senior Project Manager you will use your preclinical development expertise to manage a number of projects and oversee a small team of project managers to plan and manage preclinical developments (pharmacology, toxicology, manufacture) together with writing regulatory documents.

This is an office-based role requiring scientific and regulatory rigour as well as problem solving and outstanding communication skills.

Key duties and responsibilities:

The duties will be varied but will principally comprise:

  • Participating in prospection and scoping phases of projects for which you are a prospective Project Leader in close collaboration with the Project Management Office (PMO)
  • Project leadership and management of preclinical development programmes
  • Client liaison
  • Team management : direct, oversee and coach a small team of project managers
  • Preparing development plans
  • Writing Requests For Proposals, selecting and negotiating with service providers for out-sourced manufacturing and laboratory-based activities
  • Management and monitoring of out-sourced activities
  • Writing regulatory documents for CTAs and other regulatory filings

Mobilité géographique :



  • You hold a Ph.D. or equivalent in Biological Sciences, Chemistry, Pharmacology or other appropriate scientific discipline
  • You have several years of experience in formal preclinical development encompassing pharmacology, CMC, toxicology and regulatory affairs
  • You have excellent English oral, written and presentation skills as well as a basic ability in spoken and written French
  • You are a confident and effective communicator, able to manage multiple activities to agreed deadlines.
  • You can inspire, motivate and guide a team
  • You collate and process information in an intuitive, analytical, meticulous and conceptual manner: your problem-solving skills are outstanding
  • You are motivated by team work, responsibility, curiosity and altruism
  • You are dynamic, proactive, determined, sociable and objective; with calm self-assurance

This will be a permanent position with opportunities for growth and promotion, based in Paris (France), with a competitive salary, together with a bonus scheme awarding outstanding performance. 

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