Investigator Questionnaire Use this form to submit your information in the Investigator Database.Legal Site Name* Address* Street Address (Please include Suite, building, room number if applicable) City State / Province / Region ZIP / Postal Code AfghanistanAlbaniaAlgeriaAmerican SamoaAndorraAngolaAnguillaAntarcticaAntigua and BarbudaArgentinaArmeniaArubaAustraliaAustriaAzerbaijanBahamasBahrainBangladeshBarbadosBelarusBelgiumBelizeBeninBermudaBhutanBoliviaBonaire, Sint Eustatius and SabaBosnia and HerzegovinaBotswanaBouvet IslandBrazilBritish Indian Ocean TerritoryBrunei DarussalamBulgariaBurkina FasoBurundiCambodiaCameroonCanadaCape VerdeCayman IslandsCentral African RepublicChadChileChinaChristmas IslandCocos IslandsColombiaComorosCongo, Democratic Republic of theCongo, Republic of theCook IslandsCosta RicaCroatiaCubaCuraçaoCyprusCzech RepublicCôte d'IvoireDenmarkDjiboutiDominicaDominican RepublicEcuadorEgyptEl SalvadorEquatorial GuineaEritreaEstoniaEswatini (Swaziland)EthiopiaFalkland IslandsFaroe IslandsFijiFinlandFranceFrench GuianaFrench PolynesiaFrench Southern TerritoriesGabonGambiaGeorgiaGermanyGhanaGibraltarGreeceGreenlandGrenadaGuadeloupeGuamGuatemalaGuernseyGuineaGuinea-BissauGuyanaHaitiHeard and McDonald IslandsHoly SeeHondurasHong KongHungaryIcelandIndiaIndonesiaIranIraqIrelandIsle of ManIsraelItalyJamaicaJapanJerseyJordanKazakhstanKenyaKiribatiKuwaitKyrgyzstanLao People's Democratic RepublicLatviaLebanonLesothoLiberiaLibyaLiechtensteinLithuaniaLuxembourgMacauMacedoniaMadagascarMalawiMalaysiaMaldivesMaliMaltaMarshall IslandsMartiniqueMauritaniaMauritiusMayotteMexicoMicronesiaMoldovaMonacoMongoliaMontenegroMontserratMoroccoMozambiqueMyanmarNamibiaNauruNepalNetherlandsNew CaledoniaNew ZealandNicaraguaNigerNigeriaNiueNorfolk IslandNorth KoreaNorthern Mariana IslandsNorwayOmanPakistanPalauPalestine, State ofPanamaPapua New GuineaParaguayPeruPhilippinesPitcairnPolandPortugalPuerto RicoQatarRomaniaRussiaRwandaRéunionSaint BarthélemySaint HelenaSaint Kitts and NevisSaint LuciaSaint MartinSaint Pierre and MiquelonSaint Vincent and the GrenadinesSamoaSan MarinoSao Tome and PrincipeSaudi ArabiaSenegalSerbiaSeychellesSierra LeoneSingaporeSint MaartenSlovakiaSloveniaSolomon IslandsSomaliaSouth AfricaSouth GeorgiaSouth KoreaSouth SudanSpainSri LankaSudanSurinameSvalbard and Jan Mayen IslandsSwedenSwitzerlandSyriaTaiwanTajikistanTanzaniaThailandTimor-LesteTogoTokelauTongaTrinidad and TobagoTunisiaTurkeyTurkmenistanTurks and Caicos IslandsTuvaluUS Minor Outlying IslandsUgandaUkraineUnited Arab EmiratesUnited KingdomUnited StatesUruguayUzbekistanVanuatuVenezuelaVietnamVirgin Islands, BritishVirgin Islands, U.S.Wallis and FutunaWestern SaharaYemenZambiaZimbabweÅland Islands Country Please fill out all address lines. If your address does not have one of the lines, enter N/AMain Site Phone*Main Site Fax*Main Site Email Address* Website Type of Site (Check One) Combined Private Practice and Research Site Clinical Research Site (Patients not treated outside of clinical research studies) Private Hospital-based Site University/Academic-based Site Government Institution Site Are you affiliated with? SMO (Site Management Organization) Network of Independant Sites Additional Information if part of SMO or NetworkSMO/Network Name: Contact Name: Phone: Email: Fax: Address:What type of IRB/Ethics Committee can your site utilize? Local Central Please complete the following for each investigator at your site (first & last name, title, Medical/Therapeutic Specialty):*What is your therapeutic specialty?*AnesthesiologyCardiologyDermatologyEmergency MedicineEndocrinologyGastroenterologyGeriatricsHematologyImmunologyInfectious DiseaseInternal Medicine/Family PracticeNephrologyNeurologyOb/GynOncologyOphthalmologyOrthopedicsOtherOtolaryngologyPediatricsPharmacologyPhysical Medicine/RehabPodiatryPreventive MedicinePsychiatryPulmonologyRadiologyRheumatologySurgeryUrologyPlease check each box that corresponds to the trials you have experience in:* Allergy Angina Anxiety Arrhythmia Arthritis Asthma Atrial Fibrillation Benign Prostatic Hyperplasia Cardiovascular Device Cerebrovascular Event (acute) Cerebrovascular Event (outpatient) Chronic Obstructive Coronary Disease Congestive Heart Failure Coronary Artery Bypass Graft Coronary Artery Disease (acute/inpatient) Coronary Artery Disease (outpatient) Depression Diabetes Type I Diabetes Type II Diabetic Nephropathy Diabetic Neuropathy Diabetic Retinopathy End Stage Renal Disease Erectile Dysfunction Fibromyalgia Gastroesophageal Reflux Disease Growth Hormone Abnormalities Headache/Migraine Hormone Replacement Therapy Hyperlipidemia Hyperlipidemia, Familial Hypertension Interventional Cardiac & Vascular Procedure Irritable Bowel Syndrome Metabolic Syndrome Movement Disorders Obesity Oncology Osteoporosis Otitis Media Overactive Bladder Pain Management Parkinson's Disease Pediatric Diabetes Pediatric Hypercholest-erolemia Pediatric Hypertension Peripheral Vascular Disease Phase I Unit Psoriasis Rheumatoid Arthritis Rosacea Sexual Dysfunction Sexually Transmitted Disease Smoking Cessation Thyroid Disorders Ulcerative Colitis Women's Health Studies Other For Investigators outside of the U.S.: By submitting information on this webpage to Medpace, I am consenting to the collection and transfer of my personal data out of the country where I reside. I have read Medpace’s privacy policy https://www.medpace.com/privacy-policy/ and understand that under the law of the EU and some other countries, I have the right to access, modify or delete personal data, or to elect not to have personal data disclosed to a third party or used for any purpose materially different from the purposes stated herein. The purpose of collecting personal information about an investigator physician on this webpage is to allow Medpace to quickly identify and contact physicians for participation in clinical studies. If I wish to exercise any of the rights above, I may contact Medpace at privacy@medpace.com. I consent Please check the box below before submitting the form.
