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Fill out the form below to sign up as an investigator.
I agree to give Aptiv Solutions permission to contact me with clinical research opportunities
This profile is being completed by:
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First
Last
What is your primary role at this site?
Principal Investigator
Sub-Investigator
Study Nurse
Study Coordinator
Investigator Name:
First
Last
Degree(s):
DO
MD
RPH
MS
MPH
PHD
MSN
MBA
Title:
Please select one
Dr.
Professor
Miss
Sir
Ms.
Mr.
Address/contact details where you wish to be contacted with potential studies:
Street Address
Address Line 2
City
State / Province / Region
Zip / Postal Code
Afghanistan
Albania
Algeria
American Samoa
Andorra
Angola
Antigua and Barbuda
Argentina
Armenia
Australia
Austria
Azerbaijan
Bahamas
Bahrain
Bangladesh
Barbados
Belarus
Belgium
Belize
Benin
Bermuda
Bhutan
Bolivia
Bosnia and Herzegovina
Botswana
Brazil
Brunei
Bulgaria
Burkina Faso
Burundi
Cambodia
Cameroon
Canada
Cape Verde
Central African Republic
Chad
Chile
China
Colombia
Comoros
Congo, Democratic Republic of the
Congo, Republic of the
Costa Rica
Côte d'Ivoire
Croatia
Cuba
Cyprus
Czech Republic
Denmark
Djibouti
Dominica
Dominican Republic
East Timor
Ecuador
Egypt
El Salvador
Equatorial Guinea
Eritrea
Estonia
Ethiopia
Fiji
Finland
France
Gabon
Gambia
Georgia
Germany
Ghana
Greece
Greenland
Grenada
Guam
Guatemala
Guinea
Guinea-Bissau
Guyana
Haiti
Honduras
Hong Kong
Hungary
Iceland
India
Indonesia
Iran
Iraq
Ireland
Israel
Italy
Jamaica
Japan
Jordan
Kazakhstan
Kenya
Kiribati
North Korea
South Korea
Kuwait
Kyrgyzstan
Laos
Latvia
Lebanon
Lesotho
Liberia
Libya
Liechtenstein
Lithuania
Luxembourg
Macedonia
Madagascar
Malawi
Malaysia
Maldives
Mali
Malta
Marshall Islands
Mauritania
Mauritius
Mexico
Micronesia
Moldova
Monaco
Mongolia
Montenegro
Morocco
Mozambique
Myanmar
Namibia
Nauru
Nepal
Netherlands
New Zealand
Nicaragua
Niger
Nigeria
Norway
Northern Mariana Islands
Oman
Pakistan
Palau
Palestine
Panama
Papua New Guinea
Paraguay
Peru
Philippines
Poland
Portugal
Puerto Rico
Qatar
Romania
Russia
Rwanda
Saint Kitts and Nevis
Saint Lucia
Saint Vincent and the Grenadines
Samoa
San Marino
Sao Tome and Principe
Saudi Arabia
Senegal
Serbia and Montenegro
Seychelles
Sierra Leone
Singapore
Slovakia
Slovenia
Solomon Islands
Somalia
South Africa
Spain
Sri Lanka
Sudan
Sudan, South
Suriname
Swaziland
Sweden
Switzerland
Syria
Taiwan
Tajikistan
Tanzania
Thailand
Togo
Tonga
Trinidad and Tobago
Tunisia
Turkey
Turkmenistan
Tuvalu
Uganda
Ukraine
United Arab Emirates
United Kingdom
United States
Uruguay
Uzbekistan
Vanuatu
Vatican City
Venezuela
Vietnam
Virgin Islands, British
Virgin Islands, U.S.
Yemen
Zambia
Zimbabwe
Country
Phone Number
Email
Please check all the following Therapeutic Areas for which you have current experiences and/or interest in conducting studies:
Allergy & Immunology
Anesthesia
Cardiology
Dentistry
Dermatology
Emergency Medicine
Endocrine/Metabolism
Epidemiology
Gastroenterology
Genitourinary
Genetics
Gerontology
Hematology
Infectious Diseases
Intensive Care
Internal Medicine
Medical Devices
Nephrology
Neurology
Obstetrics/GYN
Oncology
Ophthalmology
Orthopedics
Otolaryngology
Pediatrics
Psychiatry
Pulmonology
Radiology
Rheumatology
Surgery
Transplant
Vascular Disease
What age group(s) does your site see? (select all that apply):
Pediatric
Adult
Geriatric
How long have you been conducting clinical trials?
What is the total number of trials that you have conducted as a Principal Investigator?
0 - 2
3 - 8
9 - 14
15+
What is the total number of trials by phase that you have conducted as a Principal Investigator?
Phase I
Phase II
Phase III
Phase IV
How much time do you devote each week to clinical research as a Principal Investigator?
Less than 10 hours
10 - 30 hours
More than 30 hours
Does your site have experience with Electronic Data Capture (EDC) studies?
Yes
No
Is the Investigator fluent in English?
Yes
No
Does your site conduct research through a Site Management Organization (SMO) or network?
Yes
No
What type of hospital are you affliated with?
Community Medical Center
Dedicated Research Center
General Hospital
Private Hospital
Public Health/Military/Veteran's Hospital
Rehabilitation Center
University Hospital/Medical Center
What type of IRB/EC is your site able to use?
Local
Central (independent from your site, example WIRB)
Both Central and Local
What is your Practice/Research Organization Name:
What type of Practice/Research Organization is it? (Check all that apply):
Clinic
Clinical Trial Management Organization
Group Practice
Multi-Specialty
Primary Care Center
Private Practice
Research Center
Research Organization
Number of physicians in the Practice:
Number of investigators in the Practice:
What types of trials are you interested in conducting? (check all that apply):
Outpatient Trials
Inpatient Trials
Please feel free to provide any further information about your site, its experiences and/or interests in the space below:
Thank you for completing your profile with Aptiv Solutions. We will contact you when we have upcoming trials that match your experiences and interests based on this profile.
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