Hans Tielemans Email and Phone Number
20+ years experience in clinical research in both the pharma and medical device industry as a Study co-ordinator, CRA, Global / European project / program manager; manager clinical research (including line-management), manager Medical Affairs and Director Clinical Affairs.15+ years experience in training and training management for pharma, biotech and medical devices companies.Specialties and goals: focus on small and mid-sized companies.1) Make research programs successful:• Program Management: Setting up study programs as from protocol concept till publication / presentation, including selection of resources.• Project management of (very) complex clinical studies • KOL management• On-site and remote case support - training of physicians during (emergency) patient treatment2) Make people grow and excel: • Training management • People management Experience : • 5 years of EMS experience (voluntary basis)• 8 years of nursing (geriatric wards, emergency, intensive care unit and COVID unit) • 13 months of study co-ordinating experience at anesthesia department (University Hospital Leuven) •
Sensome
View- Website:
- sensome.com
- Employees:
- 23
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Clinical Lead - Clinical ExpertSensome Sep 2020 - PresentParis, Île-De-France, FranceSensome has developed the Clotild Smart Guidewire System which will be tested in a First In Human Clinical Study in patients suffering from Ischemic Stroke.Geographical reach: Australia and Europe. - Additional projects started with Sensome's technology: in Peripheral Arterial Disease and Lung Cancer. - Training internal Sensome staff member to take role of Clinical Lead and continued Clinical support. -
Medical Affairs / Clinical Research / Training Manager / Clinical Field Specialist (Freelance)Rispondo B.V.B.A. Oct 2007 - PresentLeuvenProviding consultancy services for - medical devices companies with preference for start-up companies- CR and/or medical affairs services- pharmaceutical companies. - contract research organisationsConsultancy areas include: - Setting up Clinical Research Programs / Project Teams- Project management, - Site management- Training & training management - People management, - Medical Affairs / medical information / KOL relations- Clinical case support
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Driving InstructorErasmus Driving School Sep 2014 - PresentLeuvenIntroduction: traffic, defensive driving, driving techniquesBasic training (how to drive car)Advanced training (how to become a defensive driver in different types of traffic). Preparation for practical exams.Giving training to parents and other tutors (vormingsmoment) supervising student-drivers during their learning curve
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Field Clinical EngineerCardionomic, Inc. Jun 2021 - Oct 2023BelgiumOn-Site Case Support (proctor role) for study investigating Neurostimulation for the treatment of Acute Decompensated Heart Failure. Purpose of Neurostimulation is to increase the contractility of the heart leading to increased cardiac output. Training received in Paraguay - June 2021. Geographical reach: Belgium, Netherlands, Poland, Slovakia, Hungary. -
Director Clinical AffairsEndo Tools Therapeutics Jun 2019 - Jun 2021Brussels Area, Belgium•Setting up Clinical Affairs Structure •Starting up Investigator Initiated Studies / Sponsor Initiated Studies aiming reimbursement for the medical device.•Clinical Field Support activities - providing on-site case support in Endoscopic Bariatric Therapies in different countries in Europe -
Registered NurseSchakelzorgcentrum Pellenberg Apr 2020 - Jun 2020Pellenberg, Flemish Region, BelgiumWorking as a part-time nurse at Covid step-down unit till closure of this temporary ward.
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European Program / Project Manager (Consultant)Zoll Circulation Jul 2014 - Mar 2019EuropeManaging Therapeutic Hypothermia in STEMI Program in Europe - Program consist out of 3 complex studies (FIM, Pilot, Pivotal trial).Indication: Myocardial Infarction (STEMI)Number of study centers: up to 50 Geographical reach: up to 22 countries in Europe Activities include: - setting up and leading the European Clinical Research group, team, - country and site selection, - creation of study related procedures and documents, - KOL management, - on-site case… Show more Managing Therapeutic Hypothermia in STEMI Program in Europe - Program consist out of 3 complex studies (FIM, Pilot, Pivotal trial).Indication: Myocardial Infarction (STEMI)Number of study centers: up to 50 Geographical reach: up to 22 countries in Europe Activities include: - setting up and leading the European Clinical Research group, team, - country and site selection, - creation of study related procedures and documents, - KOL management, - on-site case support, - technical training - project management for 3 complex medical devices clinical studies. Show less
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Study NurseColoplast (Freelance Via Qps) Apr 2016 - Jul 2016BelgiumStudy nurse activities for short product evaluation study - evaluation of new intermittent urinary catheter in men.Activities include: subject recruitment and consenting, follow up of study patients at their home. Study terminated July 2016
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European Clinical Specialist - Neurovascular (Freelance)Covidien Dec 2013 - Jul 2014Paris Area, FranceIndication: stroke management (TPA with / without thrombectomy)Training of site - and CRO staff.Activities to enhance recruitment and protocol compliance Geographical reach: several countries in Western Europe. -
Training Management Specialist (Freelance)Biocartis Jan 2013 - Feb 2014Mechelen- coordinating training activities for ISO certification- induction program coordination
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Study NurseColoplast (Freelance Via Qps) Aug 2013 - Jan 2014BelgiumStudy nurse activities for short ileostomy patient material study - comparison of two types of ileostomy material. Activities included: support for IEC submission, defending investigation at IEC, subject recruitment and consenting, follow up of study patients at their home.Second highest recruting center in EU.Study terminated December 2013
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Training Management Specialist (Freelance)Thrombogenics Oct 2012 - Jan 2014Leuven- Coordinating pre product launch mandatory trainings- Setting up e-Learning portal- Creation on-boarding program- .... -
Head Of Training (Freelance)The Clinical College Part Of Novellas Healthcare Jul 2009 - Nov 2012Brussels Area, Belgium- set-up training department- develop training offer (open and in-company)- search trainers best in class- post-training evaluations of content and trainers- business development- trainer for clinical research trainings- coach
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Clinical Project Manager (Consultant Via Novellas Healthcare)Biogen Idec Nov 2009 - Jan 2011Diegem, Belgiumset up of non-interventional study in Belgium. -
Trainer / Line Manager (Freelance)Dedevan (Novellas Healthcare Flexible Staffing Solutions) Oct 2008 - Feb 2010Wemmel, BelgiumLine management of outsourced clinical research professionalsTrainer for outsourced clinical research professionals
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Advisor On Clinical Research Program (Consultant Via Novellas Healthcare)Fugeia 2009 - 2010Leuven, Belgium
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Trainer (Freelance)Covidien Jun 2008 - Jun 2009Elancourt, France- training of EU and local product specialists - Science Based Selling Skills -
Audit Support (Freelance)Cordis Feb 2009 - Apr 2009Waterloo, Belgiumproviding support to Cordis Audit team to facilitate submission to competent authorities -
Global Trial Leader (Consultant Via Mediconsult)Merck Serono Oct 2007 - Oct 2008Overijse, BelgiumSponsor oversight of several global studies in Parkinson's Disease Therapautic area -
Medical Writer (Consultant Via Docs International)Vitatron (Medtronic) Nov 2007 - Feb 2008Nijmegen Area, NetherlandsFinal study report writing
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Manager Medical Affairs - Endovascular / NeurovascularCordis, Johnson & Johnson Feb 2007 - Oct 2007- overview investigator initiated studies- liaise with marketing and sales departments- medical information management- congress support- ...newly created function - prior part of the Manager Clinical Research Function -
Manager Clinical ResearchCordis, Johnson & Johnson Jan 2005 - Jan 2007 -
Project Leader Clinical ResearchCordis, A Johnson & Johnson Company Nov 2000 - Dec 2004 -
Clinical Research AssociateCovance Sep 1997 - Nov 2000 -
Study Co-OrdinatorUniversity Hospital Leuven Aug 1996 - Sep 1997Coordination of different studies being conducted at the department of anaesthesia, University Hospital Leuven, Belgium.Tasks included: first contacts with study sponsor, negotiations of study contracts, activities related to the ethical review process, performing study activities not comprised in the normal hospital care, completing case report forms, reviewing case report forms with sponsor CRA, invoicing to study sponsor
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ParamedicusZiekenwagen Aarschot 1985 - 1990Aarschot, Vlaanderen, BelgiëEmergency care - first patient contact (eg. car accidents, pathology requiring urgent intervention)
Hans Tielemans Education Details
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Lean Sensei - Vancouver, CanadaBlack Belt Takumi Leadership Program -
Hospital Sciences And Management -
Coaching & CoProfessional Coach -
Registered Nurse -
Syntra LeuvenCertified Driving Instructor -
Syntra MechelenInternet Marketing -
Med Dev Solutions2 Day Course June 18-19 2019, Whitchurch, Uk
Frequently Asked Questions about Hans Tielemans
What company does Hans Tielemans work for?
Hans Tielemans works for Sensome
What is Hans Tielemans's role at the current company?
Hans Tielemans's current role is Clinical Research / On-Site Case Support Professional (consultant).
What schools did Hans Tielemans attend?
Hans Tielemans attended Lean Sensei - Vancouver, Canada, Katholieke Universiteit Leuven, Coaching & Co, Ku Leuven, Katholieke Hogeschool Leuven, Syntra Leuven, Syntra Mechelen, Med Dev Solutions.
Who are Hans Tielemans's colleagues?
Hans Tielemans's colleagues are Instent Sas, Guillaume Haage, Florian Miceli, Maximilien Lessault, Cécile Jouclas, Benoit Deruyver, Quentin Cavalié.
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