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Brussels, Belgique

Scientific Project Manager (M/F)

  • Experience 6 to 10 years
  • Type of role R&D, Science & Technology
  • Region Brussels
  • Activity Pharmaceuticals

Contact Cécile Deldinne
Email
+32 (0)495 80 29 81

More info on Eleonor

Founded in 2007, ELEONOR is an R&D center specialized in improving the bioavailability and bio-accessibility of poorly soluble natural ingredients for the Food Supplement, Health & Wellness markets, both human and animal.

Their mission is to transform poorly soluble, science-based active ingredients into high-performance, instantly cold-water dispersible and soluble powders with enhanced bioavailability and efficacy. ELEONOR also customizes and produces high-performance ingredients with specific functionalities for brands and ingredient manufacturers, giving them a competitive edge in the marketplace.

Find out more about the company on their website: https://leohb.com/

In order to strengthen ELEONOR’s team, we are looking for a Scientific Project Manager (Clinical & Preclinical Research, Nutraceuticals).

Responsibilities

As a Scientific Project Manager, you will play a central role in coordinating and advancing ELEONOR’s preclinical and clinical research programs. You will act as a strategic interface between our internal laboratory and external stakeholders, ensuring scientific rigor, regulatory compliance, and timely project delivery.

Your main responsibilities include:

  • Coordinate and manage CROs for preclinical and clinical studies.
  • Review, validate, and challenge study protocols to ensure scientific rigor and regulatory compliance.
  • Design and oversee R&D plans to support regulatory approvals (GRAS, Novel Food, international).
  • Act as the strategic interface between the internal lab, senior management, and external stakeholders.
  • Prepare and disseminate scientific communications (publications, conferences, marketing support).

Profile

  • Advanced degree in Life Sciences, Pharmacy, Nutrition, or related field (Master’s/PhD).
  • 5–15 years’ experience in preclinical/clinical research project management and CRO coordination.
  • Proven expertise in regulatory processes (GRAS, Novel Food, international approvals).
  • Strong knowledge of physiopathology, bioavailability, and biomarker selection.
  • Excellent project management, scientific communication, and funding application skills.

Offer

  • A stimulating, innovation-driven environment.
  • High degree of autonomy in your role, with the opportunity to contribute to unique projects.
  • Attractive prospects for personal and professional growth within a dynamic organization.

Your application will be handled with strict confidentiality

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