As a drug developer at Leads To Development you will benefit from a unique opportunity to use your scientific expertise to contribute to/and run multiple drug development projects for a wide range of innovative therapies across many different disease indications. Working as part of a young dynamic team, you will interact with clients, service providers and regulatory authorities nationally and internationally to plan and manage drug development projects. You will also play a key role in writing regulatory documents such as clinical trial applications. We are particularly seeking candidates with a background in chemistry and an interest in managing CMC (manufacture) aspects of drug development.
This is an office-based role requiring scientific insight and regulatory rigour as well as outstanding problem-solving and communication skills.
Key duties and responsibilities:
The duties will be varied and dependent on the level of experience of the successful candidate, but will principally comprise:
Project leadership and management of preclinical and clinical development programmes
Client liaison
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, including drug substance and drug product manufacturing
Critical review and analysis of scientific data
Writing regulatory documents for clinical trial applications and other regulatory filings
You hold an MSc or a PhD or equivalent in Chemistry, Pharmacy or another appropriate scientific discipline.
You have 1-5 years experience in a drug development environment
You have excellent English oral, written and presentation skills
You are a confident and effective communicator, able to manage multiple activities to agreed deadlines
You collate and process information in an intuitive, analytical, meticulous and conceptual manner; your problem-solving skills are outstanding
You are motivated by teamwork, and responsibility, and enjoy gaining new skills and knowledge
You are dynamic, proactive, determined, and objective
This will be a permanent position with excellent opportunities for growth and promotion. It is based in Paris (France), with a competitive salary and a performance-based profit-sharing scheme.
To apply please provide a CV and cover letter outlining your experience, motivation and suitability for this role. Both documents should be in English and in PDF format.
The recruitment process will be initiated with a short informal virtual meeting to discuss your background and motivation. This is followed by more comprehensive and technical interviews with the company’s management.
Leads To Development
Part of the Clarenta Group, Leads to Development provides specialist expertise in preclinical, manufacturing, regulatory and other non-clinical aspects of drug development to the biotechnology and pharmaceutical industry. As an internationally renowned drug development consultancy and management com...
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