Clément Tran

Clément Tran Email and Phone Number

Head of Clinical Affairs and Regulatory Affairs @ Lépine
Lyon, FR
Clément Tran's Location
Greater Lyon Area, France
Clément Tran's Contact Details

Clément Tran personal email

n/a
About Clément Tran

Life science, strong clinical trials background with advanced project management skill.Pharma and Vaccines clinical development, Medical Devices (Orthopedics) Clinical Evaluation & Clinical Studies, out of 27-year experience in Clinical Research.

Clément Tran's Current Company Details
Lépine

Lépine

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Head of Clinical Affairs and Regulatory Affairs
Lyon, FR
Employees:
336
Clément Tran Work Experience Details
  • Lépine
    Head Of Clinical Affairs And Regulatory Affairs
    Lépine
    Lyon, Fr
  • Groupe Lepine
    Head Of Clinical Affairs
    Groupe Lepine Aug 2021 - Present
    Genay, Auvergne-Rhône-Alpes, France
    As Director reporting directly to President and member of the Executive Committee, my mission is to lead the Clinical Affairs team to collect, review and evaluate clinical data on the Company’s devices, contributing to the company’s ability to design and market its products throughout their life cycle on all targeted markets.
  • Wright Medical
    Head Of Clinical Research
    Wright Medical Apr 2018 - Aug 2021
    Région De Grenoble, France
    Reporting to Global Director, Clinical Affairs my mission is to lead the French Clinical Research team and deliver clinical data on the Company’s devices, contributing to the company’s ability to design and market its products throughout their life cycle on all markets out of US. I achieve mission by :- Leading and developing the Clinical Research Team (CPM, DataManager, Assistant)- Ensuring that Clinical Research activities (Clinical Studies, Post-marketing registries, Investigator Initiated Studies…) are performed within defined performance criteria (budget, timing and quality), according to the local Regulations and the highest Ethics & Compliance company’s standards- Improving the processes within Clinical Research department and with interfaces.
  • Ppd
    Global Project Manager, Infectious & Respiratory Diseases
    Ppd Jan 2017 - Apr 2018
    Ivry-Sur-Seine
    Overall coordination and management of clinical trials from start up through close out. Direct technical and operational aspects of the projects, ensuring all deliverables meet the customer's expectations in terms of time/quality/cost.Monitor and analyse project parameters, milestones, risks and provide Sponsor with timely project updates.
  • Sanofi Pasteur Msd
    Head Of Planning And Project Management, Development
    Sanofi Pasteur Msd Oct 2015 - Dec 2016
    Région De Lyon, France
    Reporting to VP Development, my mission is to:- Implement PPM best practices, metrics/dashboards and develop strong collaboration relationship across Development organization- Manage Dev functions activities portfolio & projects portfolio, implement tool to provide visibility and facilitate decision making at function/project and Executive levels- Plan and execute department-wide projects that align with business priorities
  • Sanofi Pasteur Msd
    Head Of Clinical Operations
    Sanofi Pasteur Msd Mar 2013 - Oct 2015
    Région De Lyon, France
    My mission is to oversee the clinical trials execution in order to deliver clinical data with the best Quality/Cost/Time balance.I achieve my mission by- leading and developing the clinical operations staff (Clinical Trial Managers and Clinical Trial Assistants)- providing strategic direction for out-sourcing- developing and implementing processes and systems related to operational activities.
  • Sanofi Pasteur Msd
    Senior Clinical Projects Leader
    Sanofi Pasteur Msd Jun 2010 - Mar 2013
    Fully accountable for Timelines, Quality and Cost of International vaccines clinical trials.Covered countries: Belgium, Canada, Denmark, Finland, France, Germany, Italy, Spain, Sweden, and UK.Acting as a Project Leader in a matrix organisation, I am in charge of:▫ Development of Protocol, Project sizing and Planning,▫ Supervision of study documents development such as Informed Consent Form, Case Report Form, Diary Card, Study Specific Procedures and Guidelines,▫ Regulatory submissions and contracts negotiation,▫ CROs selection and study budget forecast and management (ranging from 1.5 to 5 million € per study),▫ Country affiliates and shareholders liaison, supervision of investigational sites selection,▫ Organisation and Chair of Investigators Meetings, participation to CRA training.
  • Sanofi Pasteur Msd
    Clinical Projects Coordinator
    Sanofi Pasteur Msd Oct 2005 - May 2010
    Project coordination in a matrix organisation: ▫ Development of study documents, ▫ Project Planning,▫ Development of Study Specific Procedures and Guidelines, ▫ Regulatory submissions preparation, ▫ CROs selection and study budget monitoring, ▫ Investigational sites selection, ▫ Participation to CRA training and Investigators Meetings.
  • Sanofi Pasteur Msd
    Central Cra
    Sanofi Pasteur Msd Sep 2003 - Sep 2005
    ▫ Global coordination of activities related to monitoring and management of monitoring CRO.▫ Development of study documents
  • Pharmascan
    Cra
    Pharmascan Jul 2000 - Sep 2003
    Phase I to IV clinical trials monitoring and coordination:▫ Several therapeutic areas such as dermatology, gynaecology, ophthalmology, paediatric, ▫ Different medical structures such as hospital, clinical investigation centre (CIC) and private practices
  • Laboratoire Dermscan
    Research Technician
    Laboratoire Dermscan Aug 1994 - Jun 2000
    Clinical safety evaluation of drugs and cosmetics (in-vivo on human tests) and pre-clinical safety evaluation (in-vivo on animal and in-vitro tests)

Clément Tran Skills

Budget Monitoring Cro Surveillance Clinique Sciences De La Vie Clinical Research Biotechnologie Quality Assurance Bonnes Pratiques Cliniques Essais Cliniques Matrix Management Gestion De Projet Clinical Monitoring Clinical Development Oncologie Vaccins Project Management Secteur Pharmaceutique Line Management Recherche Clinique

Clément Tran Education Details

Frequently Asked Questions about Clément Tran

What company does Clément Tran work for?

Clément Tran works for Lépine

What is Clément Tran's role at the current company?

Clément Tran's current role is Head of Clinical Affairs and Regulatory Affairs.

What is Clément Tran's email address?

Clément Tran's email address is ct****@****msd.com

What schools did Clément Tran attend?

Clément Tran attended Faculté De Médecine Saint Antoine_paris, Conservatoire National Des Arts Et Métiers / Cnam, Université Catholique De Lyon.

What skills is Clément Tran known for?

Clément Tran has skills like Budget Monitoring, Cro, Surveillance Clinique, Sciences De La Vie, Clinical Research, Biotechnologie, Quality Assurance, Bonnes Pratiques Cliniques, Essais Cliniques, Matrix Management, Gestion De Projet, Clinical Monitoring.

Who are Clément Tran's colleagues?

Clément Tran's colleagues are Maïté Blaret, Floriane Jourjon, Thomas Genon, Séverine Saint-Cyr, Loic Pfaifer, Christophe Gross, Cécile Thébault.

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