Drug Development Project Lead - Chemistry & CMC (Paris)

Leads To Development; Paris; On-site; EUR 65,000 - 95,000; Full time

Benefits offered by this job

Profit-sharing scheme

Job summary

Leads To Development in Paris, France, seeks a drug developer to lead multiple development programmes. The role is office-based and requires MSc or PhD in Chemistry or Pharmacy, with 1–5 years in drug development.

Excellent English communication is essential, along with proactive, analytical problem-solving and teamwork. You will oversee development projects, liaise with clients and regulators, prepare plans, and write regulatory documents for clinical trial applications as part of a dynamic

Qualifications

• Excellent English oral, written and presentation skills.
• Strong scientific background in chemistry/pharmacy or related field.
• Confident and effective communicator with ability to manage multiple activities to deadlines.
• Team player with proactive and analytical mindset.
• Willingness to grow and take on responsibility in drug development.

Responsibilities

• Project leadership and management of preclinical and clinical development programmes.
• Client liaison and interaction with regulatory authorities.
• Preparing development plans and regulatory documents.
• Writing RFIs/RFPs and selecting/negotiating with outsourced manufacturing and lab providers.
• Managing and monitoring outsourced activities, including drug substance/product manufacturing.
• Critical review and analysis of scientific data.
• Writing regulatory documents for clinical trial applications and other filings.

Skills

English proficiency

Education

MSc or PhD in Chemistry/Pharmacy

Job description

Leads To Development in Paris, France, seeks a drug developer to lead multiple development programmes. The role is office-based and requires MSc or PhD in Chemistry or Pharmacy, with 1–5 years in drug development.

Excellent English communication is essential, along with proactive, analytical problem-solving and teamwork. You will oversee development projects, liaise with clients and regulators, prepare plans, and write regulatory documents for clinical trial applications as part of a dynamic