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I am a senior regulatory pharmaco-toxicologist with extensive experience (20 + years) in both biotech and blue chip international pharmaceutical companies and working as a consultant. I have a proven track record of delivering multiple small and large molecule projects to clear decision milestones, submissions to, and interactions with health authorities up to licence (e.g. IND's, IMPD's, CTD's), with full knowledge of GLP/GXP standards and regulatory guidelines (ICH, CHMP, FDA, WHO). In addition, supported a number of international projects to solve industry challenges, as well as writing regulatory position paper and guidelines (WHO).

I've worked across a number of therapeutic areas, including vaccines, CV, CNS, Oncology, Respiratory, Infectious diseases and more recently, diabetes, with a background knowledge in cell and developmental biology, immunology, molecular biology.   I have good scientific and medical writing skills with experience in writing regulatory documents, study protocols, reports, scientific papers, position papers, project proposals and scientific presentations.   



Current Experience

  • Director: Non Clinical (Toxicology/Pharmacology)

    Lyon, France
    Since March 2017
    Due Diligence

    Accountable for the delivery of the toxicology and pharmacology studies/strategy for R&D from pre phase I onwards, focused on product improvement in therapeutic area of diabetes.
    Line manager responsibilities: leading/developing the non clinical team, ensuring timely deliver and managing budgets. Put in place cost effective strategies: eg one project provided a saving of 400k plus.
    A member of the senior management team involved in partner alliance responsibilities supporting joint projects, due diligence etc.

  • Consultant non clinical regulatory services/toxicology

    Lyon, France
    Since November 2015
    Due Diligence

    Providing non clinical /toxicology support to drug/vaccine development programs; a reliable and flexible service to meet the clients needs.

    Design non-clinical toxicology and safety pharmacology strategies to support all phases of drug and vaccine development, from discovery onwards. Manage study placement at a CRO (start to finish).

    Preparation and /or review of regulatory dossiers to meet health authorities needs around the world eg IND's IMPD's, CTA's, CTD', MAA's, BLA's, including preparation of investigators brochures (non clinical section).

    Medical and scientific writing (papers, articles, abstracts) plus preparation of presentations.

    Hazard identification/Risk assessmnets - toxicology evaluations, extractable and leachables, REACH. 

    Support in due diligence. 

    Project support: putting together project bids, managing project deliverables etc. 

    If I can support your business needs or you have any questions, please do not hesitate to send me an email.


Past Experience

  • Head of Non Clinical Safety Marcy-l'Étoile, France

    January 2006 --- June 2015
    budget management

  • Global Toxicology Project Leader Alderley Edge, United Kingdom

    September 1996 --- December 2005
    Infectious diseases


Self Assessment :
AdaptabilityIndependenceInterest in knowledgeOptimismOrganizationProactivityProblem solvingResiliencySelf-confidenceSelf-disciplineSociabilityStrategic thinkingTrustDependabilityCreative thinkingCritical thinkingCuriosityDiligenceEfficiencyFlexibilityKindnessPerspectiveAnalytical thinkingAssertivenessAuthenticityCollaborationCoordinationWillingness to compromiseCommunicative


Self Assessment :
molecular biologyPhase IIIPhase IVPhases of clinical development (phase I to IV)Position PaperPowerPointPre-clinical researchPreclinical regulations and practicesPrenatal developmentProblem-solving methods and troubleshootingPhase IIPhase IMonitoring Study ProgressNegotiationNew Drug Application (NDA)oncologyPCRpeople managementPharmaceutical IndustrypharmacologyPharmacovigilanceProject ManagementProtocolTeam LeadershipToxicologyUnderstand how results translate to practiceUnderstand levels of research evidenceUnderstanding of regulatory guidelinesVaccinesWestern BlottingInformed Consent DocumentsWriting Study Procedures and SOPsSOPSerious Adverse Event (SAE)R&DRegulatory affairsRegulatory RequirementsRegulatory submissionsRespiratoryRT-PCRSafety concerns (such as therapeutic ratio with respect to possible adverse effects)Scientific methodologyScientific Writing BiochemistryMolecular & Cellular BiologyDrug and vaccine developmentBiopharmaceuticalsCross-functional team leadershipDNADNA extractionDNA sequencingDrug development processDrug regulatory authoritiesDrug safety assessmentEMABiomarkersAnimal trial R&D Scientific writing Phase IActions and modes of action of drugs in the human speciesActions and modes of action of human physiologyAllergy and immunologyAnimal ModelsEnglishFDAIMPDIn VitroIn VivoINDInfectious diseasesInflammationInformed Consent ProcessKnowledge of the drug development processMarketing Authorisation Application (MAA)ImmunologyImmunohistochemistry (IHC)GCPGood Laboratory Practice (GLP)Good Publication Practice (GPP)GynecologyHospitalsICH GCP guidelinesMedical writing Animal models Cell biologyBiological Drug DevelopmentCancerCardiovascular diseasesInternational Project ManagementToxicologyBudgetingDrug DevelopmentPreclinical Safetysafety assessmentInvestigative SafetyReport WritingSmall moleculesVaccinesadjuvants

Skills and Expertise

Self Assessment :
Conduct literature searchesCollaborate with project teamCollaborate with principal investigatorCollaborate with medical team Analyze dataAdjust processes Coordinate regular advisory boardcoordinating research projects Create SOPsCoachCoach staffDirect co-workersDevelop regulatory strategyDesign studyDesign scientific projects (in biology)Data analysisAdjust processes and methodsAssign activitiesNetworkObserve trends in dataPrepare final reportProvide benefit risk assessmentPublish scientific projectsRead medical literatureReport dataReview medical reportsManuscript preparation and reviewManuscript preparationbudgeting of R&D activitiesCommunicate with sponsorCreate study documentsCreates a collaborative team environmentExecute scientific projectsGenerate regulatory submissions Handle callsmanaging a small teamWork under specific instructions Interact with nursesWritten presentationInteract with pharmacistsInteract with nursesInteract with CROsOrganise steering committeeOrganize scientific projects (in biology)Writing regulatory documentsWrite protocolsWrite papersInteract with physiciansInteract with pre-clinical scientistsOrganise meetingsOral presentationManuscript reviewManage projects resourceslifescienceLiaise with research teamLiaise with doctorsLate-stage regulatory filing (MAA, BLA)Write medical reportsStorytellingSolve problemsAttend steering committeeAttend seminarsAttend investigator meetingAnalyze data Write papers Search literature on clinical trials Report data Interpret dataBiomarker ResearchEvaluate licensing opportunitiesReview study protocolsReport study conclusionsRegulatory submissionsRegulatory documentationProvide trainingPresent at steering committeePrepare regulatory documentsEvaluate protocols Interact with physiciansManage multiple projectscollaborate with project teamsmanage project resourcespreclinical protocolsstudy directingstudy monitoringproject probable outcomework cross functionalyManage complexityAdvise on strategy


  • Ph.D. in Biological sciences from University of Manchester in 1996
  • Bachelor of science in Applied Biology from Manchester Metropolitan University in 1992
  • Nursing in RGN from Kingston Hospital in 1987

Training and Certification

  • Coaching Psychology in 2014 Certification


BrightOwl Assessment:
Self Assessment:
Full Proficiency

Work Preferences

  • Notice Period:
    13 weeks
  • Locations I am interested in:
    Belgium France Netherlands Switzerland
  • Work From Home:
  • Work Regime:
    Permanent position
    BrightOwl freelancer :    37 hours Hours per week
  • International:

Area / Region

Lyon, France


Driving License
  • Yes

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