Clinical Project Leader F/M
Sanofi

Sanofi

Clinical Project Leader F/M

  • Zmluva na dobu neurčitú 
  • Chilly-Mazarin

Spoločnosť

Sanofi

Sanofi

  • Farmaceutický priemysel / Biotechnológie

Pracovná ponuka

Clinical Project Leader F/M

  • Zmluva na dobu neurčitú 
  • Chilly-Mazarin

Táto pozícia bola obsadená!

Who are they?

At Sanofi, we pursue the miracles of science to improve people’s lives. In France, more than 20,000 passionate men and women tirelessly push their limits to transform the practice of medicine and improve patient health with drugs and vaccines.

The desire to advance science is our strength. We want to improve the health of populations and find new solutions for patients by combining scientific progress and advanced technologies.

In France, we provide more than 400 drugs, vaccines and health products, including 18 vaccines and more than 200 drugs of major therapeutic interest.

Sanofi’s roots are anchored in France where most of the Research and Development is located. In the French medical research landscape, we hold a central role and actively participate in the construction of a dynamic health sector.

To contribute to the world of tomorrow, three commitments guide our actions: access to care for the most vulnerable, inclusion of all through work and preservation of the planet. Nothing would be possible without the remarkable mobilization of our employees and partners.

Sanofi
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Job description

Le contenu du poste est libellé en anglais car il nécessite de nombreuses interactions avec l’international, l'anglais étant la langue de travail. 

ROLES AND RESPONSIBILITIES

Purpose of the position

The role of the Clinical Project Leader is to oversee the conduct of projects (local studies, R&D, etc.) whilst ensuring compliance with current regulations, the specified timescales, budget and quality in France.

Main duties

  • Planning and undertaking all activities required for the proper conduct of their assigned project (from project feasibility or Study Outline validated to clinical study report )
  • Meeting quantitative and qualitative targets in the specified timescales
  • Setting, securing approval for and tracking the budget
  • Contributing to the files submitted to the regulatory bodies (Ethics Committee, ANSM and CNO) by providing all documents on the study (insurance, protocol, synopsis, L-ICF, etc.) and the centres (list of investigators, CV, etc.)
  • Producing the protocol, case report form, local informed consent form and subcontracting specifications for local studies
  • Providing CRO oversight for local studies
  • Designing and distributing study documents (booklet, patient cards, etc.)
  • Providing the materials and services needed to select, motivate and train study investigators and other external contributors, and intervening if necessary
  • Initiating and organizing investigator meetings
  • Overseeing monitoring activities including RBM
  • Defining the means of quality controlling clinical study data and implementing corrective action (overseeing monitoring reports, co-monitoring visit, etc.)
  • Identifying deviations (in quality, budget and timescale), proposing and implementing corrective action
  • Participating in audits, coordinating responses and overseeing potential corrective action plan
  • Notifying SAEs in the required deadlines
  • Providing a permanent interface with the Unit Head on operational aspects
  • Organizing and summarizing relevant information and sharing it with project contributors internally (R&D CTT, Medical BU team meeting, reporting significant events) and externally (newsletter, teleconference and/or investigator/CRO meeting)
  • Advising CRAs and investigators on the protocols
  • Coordinating and contributing to the training and motivation of a project team or CRO in the event of subcontracting
  • Initiating and leading project team meetings and approving the minutes

Main professional relationships

  • Internal : RTMs, CSO members, CSU members, French Medical Affairs.
  • External : Interface with sites, vendors, patients associations, CROs

BENEFITS OF WORKING IN THIS ROLE

  • Diversity of studies and pathologies. Management in the same time (3 or 4 projects…) Phase I to phase IV, registry, observational study: Rare disease, Rare blood disease, I&I, CHC, …
  • Main contact of the project in France
  • Close collaboration with medical affairs and CSO platform

REQUIRED KNOWLEDGE AND SKILLS

Professional environment

  • English
  • Leadership
  • Good interpersonal skills,
  • Coordination and project management,
  • Analytical skills,
  • Time management
  • Operational expertise

Career path (Level of studies and experience)

  • Scientific background (4/5 years)
  • Knowledge of GCP/ICH
  • Experience as a CRA will be a plus

At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers. We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all.

As part of its diversity commitment, Sanofi is welcoming and integrating people with disabilities.

Sanofi

Sanofi

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