Steven Mortier is an ambitious professional who build up over 14 years expertise in pharma R&D in oncology, infectious diseases and neuroscience, including 11 years in clinical R&D. He has a background of Biotechnology from the Ghent University and obtained an executive MBA from the Antwerp Management School.
He is a calm, inclusive and results driven colleague with an open mind, and is eager to contribute and grow further his expertise in clinical R&D coordination and project management.
Senior Clinical Scientist
Since August 2017
Lead Sr Clinical Scientist for complex global PoC programs in various indications. Leading through piloting innovative setups with several vendors.
Willingness to compromiseStrategic thinkingResult OrientedProblem solvingInterest in knowledgeInnovative thinkingIndependenceCommunicativeAnalytical thinking
BiotechnologieStrategic PlanningRisk ManagementProject ManagementProject CoordinationProblem SolvingPhase IPhase IIIPhase IIPharmaceutical ResearchPharmaceutical IndustryPharmaceutical DevelopmentPatient recruitmentOutlookOperations ManagementOncology Clinical ResearchNeuroscienceMS ProjectMolecular geneticsMicrosoft ProjectMicrosoft OfficeMicrosoft PowerpointMitigationMicrosoft WordMicrosoft ExcelInternational Project ManagementInfectious diseasesIn VivoGood Clinical Practice (GCP)Ethics submission and approval processEnglishEnglishEfficacy trialsEarly development stageDrug DevelopmentCommunication SkillsCoachingClinical trialsClinical trial managementClinical trial budgetingClinical researchClinical operationsClinical DevelopmentClinical monitoringCancer ResearchBusiness PlanningBudget ProcessBudget ManagementBiotechnologySafety trialsProject Planning
Skills and Expertise
Analytical skills Interact with physiciansAlzheimerAssess site feasibilityassess the needs of the project(s)/program(s) and make changes in process, work flow and/or assignments.Assist with proceduresAttend investigator meetingAttend seminarsAttend seminars, courses and meetings within and outside the companybudgeting of R&D activitiesBuild trial master file (TMF)CoachCollaborate with project teamcontrol different protocol versions and other essential documentsCoordinate projectscoordinating research projectsDesign clinical presentationDesign studiesDesign trial master file (TMF)Develop business planDevelop study budgetEvaluate protocolsFinancial administrationFinancial reportsInitiate clinical trials Interact with KOLLiaise with doctorsManage budgetsManage projects resourcesManage study budgetManage trial master file (TMF)Organise meetingsproject managementR&DReview protocolsReview medical reportsReview monitoring reportsReview study protocolsSelect investigatorsSolve problemsSite managementSet up a clinical studySelect sitesReview informed consent processUnderstand protocolsTranslate customer needs into analytical study proposal/protocolStudy execution planPlanning clinical studiesNetwork
Advanced Master in Business Administration (MBA) from Antwerp Management School (AMS) in 2014
Advanced Master in Laboratory Animal Science (Category C) from Gent University in 2005
Master in Biotechnology from Gent University in 2001
Training and Certification
Post Graduate Course - introduction in management in 2009 Training
Post Graduate Course - Principles in Chemotherapy in 2008 Certification
Post Graduate Course - Non-Small-Cell-Lung-Cancer in 2007 Certification
Expert has 5 publications (Will be avalible with full profile)