Senior Clinical Development Scientist: Lead Clinical Trials

Ipsen Pharma (SAS); Paris; On-site; EUR 90,000 - 130,000; Full time

Job summary

Ipsen Pharma (SAS) seeks a Senior Clinical Development Scientist to join the clinical development team and contribute to the strategy and execution of clinical studies with cross-functional partners. You will lead scientific discussions with investigators, review trial data, and ensure compliance with ICH/GCP guidelines and Ipsen SOPs throughout study execution.

The role requires strong communication, attention to detail, and the ability to thrive in a fast-paced environment, coordinating with

Qualifications

• Strong communication skills and attention to detail.
• Experience in clinical development and trial execution.
• Ability to work independently in a fast-paced environment.

Responsibilities

• Support and/or co-lead with clinical development directors the clinical team of an assigned project and provide scientific and clinical leadership in planning, conducting, and executing clinical trials.
• Review, analyze, and interpret emerging clinical trial data and prepare for study meetings with investigators, monitoring committees, and advisory boards.
• Partner with the study clinical lead and CRO medical monitor on oversight of clinical trial activities, including safety reviews and site interactions.
• Liaise with the broader clinical development team (clinical operations, data management, statistics/programming, regulatory)
• Contribute to authoring key study and regulatory documents (protocol, ICF, manuals, briefing books)
• Lead internal meetings to review topics from a clinical development perspective and develop mitigation plans
• Lead/adapt participation in advisory boards, data monitoring/steering committees and investigator meetings
• Ensure compliance with ICH/GCP guidelines, regulatory requirements, and Ipsen SOPs

Job description

Ipsen Pharma (SAS) seeks a Senior Clinical Development Scientist to join the clinical development team and contribute to the strategy and execution of clinical studies with cross-functional partners. You will lead scientific discussions with investigators, review trial data, and ensure compliance with ICH/GCP guidelines and Ipsen SOPs throughout study execution.

The role requires strong communication, attention to detail, and the ability to thrive in a fast-paced environment, coordinating with