PMO OPEN-ReMIE National clinical research project (F/M)

Date de publication : 25 avril 2025
CDD
12 mois

Localisation

69009 Lyon, Auvergne-Rhône-Alpes

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A propos

The Groupement Hospitalier Nord includes the Hôpital de la Croix-Rousse, the Hôpital Pierre Garraud and the Hôpital Frédéric Dugoujon. It offers cutting-edge care in a number of specialties, including infectious and tropical diseases, liver pathologies, obstetrics and gynecology, and geriatrics.

Votre mission

Main mission

Steering, structuring, and monitoring the activities of the OPEN-ReMIE project, integrated from the outset into the

EU-funded project EU-PROACT, an offshoot of EU-RESPONSE.

Main activities

• Overall project coordination

o Ensure day-to-day management of the project in liaison with the scientific coordinator and the Inserm Transfert

team in charge of project management

o Develop and update project management tools: work plan, schedule of deliverables, responsibilities matrix

(RACI), dashboard, etc.

o Participate in setting up and monitoring the various governance bodies

o Organize and lead steering and monitoring meetings (steering committees, technical meetings, etc.)

o Oversee the progress of work packages and ensure that deadlines and milestones are met

o Anticipate and resolve operational problems in collaboration with partners

o Participate in the drafting of scientific reports and external requests for evaluation and information

o Coordinate the production of project deliverables (scientific reports, publications, web content, events)



• Administrative and financial management

o Monitor the overall project budget, in liaison with the financial departments of partner institutions

o Contribute to active monitoring of obligations under the funding agreement, in particular to ensure that

expenditure complies with the funder's rules

o Participate in the consolidation of interim and final financial reports for the funder

o Ensure proper management of contracts with subcontractors and partners



• Quality management and regulatory compliance

o Implement and coordinate the quality procedures required for the smooth running of the project

o Prepare any audits requested by the funder or competent authorities



• Communication and dissemination

o Participate in drawing up the communication and results dissemination plan, in liaison with partners and

dedicated work packages

o Support the scientific coordinator in exchanges with external stakeholders and the media



• Coordination between clinical research platforms and networks

o Participate in inter-platform coordination meetings

o Contribute to ensuring EU-PROACT's articulation with national and European mechanisms, in particular for

funding and prioritizing clinical trials in preparation for and in response to epidemics

o Participate in work on cross-functional issues, in particular regulatory and legal aspects, the sharing and

valorization of data and results, and communication

o Help implement new strategic partnerships, with public and private partners

o Participate in discussions on the pooling of resources, and the possible creation of new clinical research



• Associated activities

o Update departmental dashboards

o Participate in drafting and validating ANRS MIE quality assurance procedures

o Participate in the drafting of activity reports and communication media, including the ANRS MIE website

networks

Job specificities and environment

• No particular constraints

Le profil idéal

Knowledge

• Good knowledge of national funding frameworks (PHRC national, RECH-MIE, etc.) and reporting tools

• Good knowledge of global health issues, particularly in relation to infectious diseases

• Understanding of regulatory frameworks for clinical research in Europe

• Fluency in English is essential

Skills

• Excellent command of project management tools

• Ability to manage complex activities and meet tight deadlines

• Facilitation of multi-stakeholder meetings

• Proven skills in budget management and financial monitoring of international projects

Aptitudes

• Rigor, autonomy, and excellent organizational skills

• Ability to work in a multicultural environment with a variety of contacts

• Team spirit and excellent communication skills

• Flexibility, adaptability, and openness to innovation

Required experience

• Significant experience (3 to 5 years minimum) in managing national and European research projects, ideally in an

academic context

• Expertise in managing multi-country research projects

• Experience in setting up national and/or international collaborative projects (Horizon Europe, ERA-NET, NIH, etc.)

Level of diploma and training

• 5-year degree in life sciences, biomedical engineering, project management or related field (Master's degree in

clinical project management, public health, or equivalent).



  • 12 mois renouvelable

  • Temps plein 39h 28 CA et 20 RTT

  • Rémunération

  • Selon les grilles de la fonction publique et en fonction de l'expérience professionnelle sur des

    postes de niveau équivalent. Précisez vos prétentions salariales

  • Avantages : Restauration collective subventionnée sur place, Comité d'action sociale (prestations sociales, culturelles, sportives).

  • Transports publics remboursés partiellement.

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