Medical Monitor

Job Description:

At Danone, we are driven by our mission: "Bringing health through food to as many people as possible." This purpose is rooted in our heritage and guides everything we do-from developing science-based nutritional solutions to promoting sustainable practices that protect our planet. As a Société à Mission, we are committed to creating both economic and social value, with a focus on health, nature, and people & communities.

Joining Danone means becoming part of a collaborative and inclusive environment where your expertise makes a real impact. You will contribute to the development of innovative, science-based nutritional solutions and help shape a healthier future for people and the planet.

As a Medical Monitor, you will play a key role in ensuring the safety and well-being of clinical study participants and upholding the integrity of the studies. You will provide medical oversight, manage serious adverse events (SAEs), support safety signal detection, and contribute to the development of safe, evidence-based nutritional products aligned with Danone's health-driven mission.

What you'll do

* Provide medical supervision across multiple clinical studies.
* Understand scientific strategic roadmaps and execute them through efficient project contribution, ensuring timely and safe delivery of clinical studies.
* Drive safety across different studies simultaneously.
* Take ownership of refining and standardising clinical safety evaluation processes, ensuring consistency and alignment with industry standards.

Your key deliverables

* Oversee clinical study activities and ensure compliance with protocols and regulatory standards.
* Act as the primary medical contact for study teams, investigators, and internal/external stakeholders.
* Contribute to protocol development, study design, and medical monitoring plans.
* Assess reported safety events and evaluate Serious Adverse Events (SAEs) promptly, including causality and expectedness, ensuring regulatory compliance and complete documentation.
* Monitor safety trends and collaborate across functions to identify potential safety signals.
* Escalate medical alerts and ensure proactive risk management.
* Review and approve essential clinical study documents (protocols, product information, safety reports, study reports) from a medical and safety perspective.
* Collaborate with cross-functional teams to ensure alignment and excellence in execution.

* A Medical Doctor’s (MD) degree.
* Experience in international clinical research, ideally within the pharmaceutical, nutrition, or healthcare sectors (a plus).
* A strong background in clinical practice, patient care, and Good Clinical Practice (GCP), with the willingness to grow into the role.
* Proven ability to collaborate effectively across multidisciplinary teams.
* A mindset focused on continuous learning, adaptability, and openness to technology and digital innovation in clinical research.
* Confidence in using digital tools and emerging technologies to enhance trial safety, efficiency, and impact.
* Excellent command of spoken and written English, with the ability to communicate clinical information clearly in study documents and presentations