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Clinical Learning Development Project Manager

Posted about 2 months ago

RemoteParis, Île-de-France, FranceSE

About the Job

Excelya is seeking a Clinical Learning Development Project Manager to join our innovative and dynamic team. The Clinical Learning & Development Project Manager is responsible for the design, development, implementation, and evaluation of continuous learning solutions supporting Clinical Sciences & Operations (CSO) and Clinical Vaccine teams. Acting as the L&D lead within project teams, the role ensures that all training activities are delivered according to project plans and aligned with business needs.

Main Responsibilities

  • Lead project teams dedicated to training and learning activities, ensuring timely and high-quality delivery of learning solutions.
  • Conduct training needs analyses through structured interviews with stakeholders and translate needs into clear learning strategies, timelines, and resource plans.
  • Design end‑to‑end learning solutions, including learning journeys, delivery methods, content outlines, and evaluation frameworks, using the ADDIE methodology.
  • Develop digital learning content and associated media using Articulate 360 (Storyline, Rise, Review) and coordinate content creation with subject‑matter experts when required.
  • Leverage AI and digital tools to support storyboard creation, voiceovers, and multimedia development across ADDIE stages.
  • Coordinate the deployment and communication of learning solutions, including the organization and delivery of instructor‑led training sessions when appropriate.
  • Evaluate learning effectiveness through feedback, assessments, and performance indicators, and drive continuous improvement.
  • Maintain and update learning solutions after deployment to ensure ongoing relevance and compliance..

Requirements

About You

  • Proven experience in managing learning and development projects, preferably within clinical research or pharmaceutical environments.
  • Proven delivery of learning solutions end‑to‑end using the ADDIE methodology.
  • Advanced proficiency with Articulate 360 Suite (mandatory).
  • Excellent project management skills with the ability to handle multiple initiatives simultaneously.
  • Strong communication and interpersonal skills with the ability to collaborate effectively across teams.
  • Proficiency with learning management systems (LMS), e-learning platforms, and digital training tools.
  • Fluency in English is required.

Benefits

Why Join Us?

At Excelya, we combine passion for science with enthusiasm for teamwork to redefine excellence in healthcare.

Here’s what makes us unique—

We are a young, ambitious health company representing 900 Excelyates, driven to become Europe’s leading mid-size CRO with the best employee experience. Our one-stop provider service model—offering full-service, functional service provider, and consulting—enables you to evolve through diverse projects. Working alongside preeminent experts, you will help improve scientific, operational, and human knowledge to enhance the patient’s journey.

Excelling with care means benefiting from an environment that values your natural talents, pushes boundaries with audacity, and nurtures your potential, allowing you to contribute fully to our shared mission.

Job details
Workplace
Remote
Location
Paris, Île-de-France, France
Experience
SE

Excelya is an independent, Paris-headquartered contract research organization (CRO) founded in 2014 that supports biotech, pharmaceutical, and medical device companies with full-service CRO, FSP, and resourcing solutions across clinical development. The company operates through a global network with 900+ experts and coverage in 25 countries, offering capabilities in areas such as clinical operations, data management, biometrics, pharmacovigilance, regulatory affairs, and medical affairs to help clients deliver clinical trials and bring new therapies to patients.

Industry
Pharmaceutical Manufacturing
Headquarters
Boulogne-Billancourt, Île-de-France
Founded
2014
Company location
Boulogne-Billancourt, Île-de-France
Specialties
Opérations cliniques, Affaires Réglementaires, Biométrie, Rédaction Médicale, Pharmacoviglance, Information Médicale, Contract Research Organisation, Biometrics and Clinical Research, Data Management, Pharmacovigilance, Medical Affairs, Biotech, Medical Devices, Clinical Trials, Drug Development Services, Oncology, Market Access, Rare Disease, Pharmaceuticals, CRO, Clinical Trial Optimization, Cell and Gene Therapy, Infectious Diseases, Immuno-Oncology, Cosmetics, and Nutrition

Key team members

Julien Sallaind

Julien Sallaind

Elitza Ouzounova

Elitza Ouzounova

Emilie Stefanelli

Emilie Stefanelli

Laurence MAUNIER

Laurence MAUNIER

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