Tampa, FL · On-site
$60 - $80/hr
Basic knowledge of clinicaltrials.gov, consenting, protocol review, adverse and serious adverse event reporting. Ability to work independently, to make decisions, to interact with sponsors ...
Tampa, FL · On-site
$60 - $80/hr
Basic knowledge of clinicaltrials.gov, consenting, protocol review, adverse and serious adverse event reporting. Ability to work independently, to make decisions, to interact with sponsors ...
Birmingham, AL · On-site
$60 - $80/hr
Basic knowledge of clinicaltrials.gov, consenting, protocol review, adverse and serious adverse event reporting. Ability to work independently, to make decisions, to interact with sponsors ...
Birmingham, AL · On-site
$60 - $80/hr
Basic knowledge of clinicaltrials.gov, consenting, protocol review, adverse and serious adverse event reporting. Ability to work independently, to make decisions, to interact with sponsors ...
Boston, MA · Hybrid
$120K - $150K/yr
Help maintain timely and accurate study registration and updates on ClinicalTrials.gov and other applicable registries. Coordinate Clinical Trial Team meetings and drive action item follow-up. ...
Boston, MA · Hybrid
$120K - $150K/yr
Help maintain timely and accurate study registration and updates on ClinicalTrials.gov and other applicable registries. Coordinate Clinical Trial Team meetings and drive action item follow-up. ...
Bethesda, MD · On-site
$56.50 - $77.25/hr
For example, NCBI develops and delivers PubMed, an index of over 29 million biomedical research abstracts; and maintains ClinicalTrials.gov, a database of over 400,000 clinical studies around the ...
Bethesda, MD · On-site
$56.50 - $77.25/hr
For example, NCBI develops and delivers PubMed, an index of over 29 million biomedical research abstracts; and maintains ClinicalTrials.gov, a database of over 400,000 clinical studies around the ...
Bethesda, MD · On-site
Overview Black Canyon Consulting (BCC) is searching for a Quality Assurance Engineer to support the ClinicalTrials.gov (CTG) program at the National Institutes of Health (NIH) in Bethesda, MD. This ...
Bethesda, MD · On-site
Overview Black Canyon Consulting (BCC) is searching for a Quality Assurance Engineer to support the ClinicalTrials.gov (CTG) program at the National Institutes of Health (NIH) in Bethesda, MD. This ...
Bethesda, MD · On-site +1
$56.50 - $77.25/hr
For example, NCBI develops and delivers PubMed, an index of over 29 million biomedical research abstracts; and maintains ClinicalTrials.gov, a database of over 400,000 clinical studies around the ...
Bethesda, MD · On-site +1
$56.50 - $77.25/hr
For example, NCBI develops and delivers PubMed, an index of over 29 million biomedical research abstracts; and maintains ClinicalTrials.gov, a database of over 400,000 clinical studies around the ...
Enter information in ClinicalTrials.gov for clinical studies prior to study initiation. Provide quality assurance for the data and information entered, and ensure compliance with the current ...
Enter information in ClinicalTrials.gov for clinical studies prior to study initiation. Provide quality assurance for the data and information entered, and ensure compliance with the current ...
Gainesville, FL · On-site
$53K - $57K/yr
Aids in clinicaltrials.gov submissions. Prepares progress reports; periodically reviews study protocols and suggests changes as needed. Reviews research projects periodically to ensure all procedures ...
Gainesville, FL · On-site
$53K - $57K/yr
Aids in clinicaltrials.gov submissions. Prepares progress reports; periodically reviews study protocols and suggests changes as needed. Reviews research projects periodically to ensure all procedures ...
Manhattan, NY · On-site
Maintain all clinical trials information on clinicaltrials.gov. Additional related duties as assigned-5%. * Manage correspondence, generate materials, and execute administrative tasks for ...
Manhattan, NY · On-site
Maintain all clinical trials information on clinicaltrials.gov. Additional related duties as assigned-5%. * Manage correspondence, generate materials, and execute administrative tasks for ...
Lake Success, NY · On-site +1
$75K - $126K/yr
Familiarity with ClinicalTrials.gov registration and maintenance, preferred * Ability to manage multiple projects and collaborate across team, preferred * Experience in an academic medical center or ...
Lake Success, NY · On-site +1
$75K - $126K/yr
Familiarity with ClinicalTrials.gov registration and maintenance, preferred * Ability to manage multiple projects and collaborate across team, preferred * Experience in an academic medical center or ...
... Clinicaltrials.gov, the mandatory trial registration process, ongoing record maintenance and final results submissions. * Provide infrastructural support and clinical research expertise to the ...
... Clinicaltrials.gov, the mandatory trial registration process, ongoing record maintenance and final results submissions. * Provide infrastructural support and clinical research expertise to the ...
Boston, MA · On-site
$120K - $150K/yr
... ClinicalTrials.gov and other applicable registries. ● Coordinate Clinical Trial Team meetings and drive action item follow-up. ● Maintain clinical operations trackers, databases, and document ...
Quick apply
Boston, MA · On-site
$120K - $150K/yr
... ClinicalTrials.gov and other applicable registries. ● Coordinate Clinical Trial Team meetings and drive action item follow-up. ● Maintain clinical operations trackers, databases, and document ...
Fort Detrick, MD · On-site
$78K - $81K/yr
Enter information in ClinicalTrials.gov for clinical studies prior to study initiation. Provide quality assurance for the data and information entered, and ensure compliance with the current ...
Fort Detrick, MD · On-site
$78K - $81K/yr
Enter information in ClinicalTrials.gov for clinical studies prior to study initiation. Provide quality assurance for the data and information entered, and ensure compliance with the current ...
... ClinicalTrials.gov registration and results reporting, aligning IRB determinations with federal and sponsor requirements. Education, Collaboration, and Special Projects • Develops, delivers, or ...
... ClinicalTrials.gov registration and results reporting, aligning IRB determinations with federal and sponsor requirements. Education, Collaboration, and Special Projects • Develops, delivers, or ...
Tempe, AZ · On-site
$80 - $100/hr
Proficiency with scientific and clinical resources including PubMed, NCCN guidelines, ClinVar, COSMIC, OncoKB, CIViC, and ClinicalTrials.gov.* Proficient in Microsoft Office Suite, including Word ...
Tempe, AZ · On-site
$80 - $100/hr
Proficiency with scientific and clinical resources including PubMed, NCCN guidelines, ClinVar, COSMIC, OncoKB, CIViC, and ClinicalTrials.gov.* Proficient in Microsoft Office Suite, including Word ...
Waltham, MA · On-site
$250/hr
Source, validate, and synthesize intelligence from clinical, competitive, and commercial databases to support decision-making (e.g., ClinicalTrials.gov, primary literature). * Cross-functional ...
Waltham, MA · On-site
$250/hr
Source, validate, and synthesize intelligence from clinical, competitive, and commercial databases to support decision-making (e.g., ClinicalTrials.gov, primary literature). * Cross-functional ...
Source, validate, and synthesize intelligence from clinical, competitive, and commercial databases to support decision-making (e.g., ClinicalTrials.gov, primary literature). * Cross-functional ...
Quick apply
Source, validate, and synthesize intelligence from clinical, competitive, and commercial databases to support decision-making (e.g., ClinicalTrials.gov, primary literature). * Cross-functional ...
Manage ClinicalTrials.gov postings as required. * Collaborate with Research Managers, Research Nurses, and Research Coordinators to identify and complete all regulatory needs for assigned protocols.
Manage ClinicalTrials.gov postings as required. * Collaborate with Research Managers, Research Nurses, and Research Coordinators to identify and complete all regulatory needs for assigned protocols.
Ann Arbor, MI · On-site
$80 - $100/hr
... at Clinicaltrials.gov.Working with Research Pharmacy, Investigational Product (IP) management and accountability * Supervision Received: This position reports directly to Faculty Principal ...
New
Ann Arbor, MI · On-site
$80 - $100/hr
... at Clinicaltrials.gov.Working with Research Pharmacy, Investigational Product (IP) management and accountability * Supervision Received: This position reports directly to Faculty Principal ...
New
Charleston, SC · On-site
Register and maintain applicable studies in ClinicalTrials.gov, including initial registration, record updates, and results reporting as required. * Prepare and maintain supporting documentation ...
Quick apply
Charleston, SC · On-site
Register and maintain applicable studies in ClinicalTrials.gov, including initial registration, record updates, and results reporting as required. * Prepare and maintain supporting documentation ...
$12.50 - $19.71
5% of jobs
$19.71 - $26.92
7% of jobs
$26.92 - $34.13
7% of jobs
$36.99 is the 25th percentile. Wages below this are outliers.
$34.13 - $41.35
13% of jobs
$41.35 - $48.56
9% of jobs
The median wage is $53.06 / hr.
$48.56 - $55.77
13% of jobs
$55.77 - $62.98
17% of jobs
$64.93 is the 75th percentile. Wages above this are outliers.
$62.98 - $70.19
13% of jobs
$70.19 - $77.40
9% of jobs
$77.40 - $84.62
4% of jobs
$84.62 - $91.83
2% of jobs
$12
$53
$91
Cities with the most Clinicaltrials Gov job openings:
The most popular types of Clinicaltrials Gov jobs are:
States with the most job openings for Clinicaltrials Gov jobs include:
The top searched job categories for Clinicaltrials Gov jobs are:
Tampa, FL • On-site
$60 - $80/hr
Other
Posted 6 days ago
7.7
Based on 44 frontline employees who took The Breakroom Quiz
265th of 631 rated colleges and universities
Job Description - CLINICAL RESEARCH REGULATORY COORDINATOR II (2) (T238047)
CLINICAL RESEARCH REGULATORY COORDINATOR II (2) - ( T238047 )
Description
The University of Alabama at Birmingham (UAB), O'Neal Comprehensive Cancer Center, is seeking a Clinical Research Regulatory Coordinator II.
The Clinical Research Regulatory Coordinator II will prepare, submit, and assist with multiple levels of research documentation, IRB submissions to UAB, WIRB, Advarra, and others. Maintain regulatory documentation, including ICF, protocol, 1572, CVs, ML, IB, recruitment materials, submission forms, and draft informed consents. Maintain/prepare FDA applications for Investigational New Drugs (INDs) and Investigational Device Exemptions (IDEs). To serve as a resource person or act as a consultant within the area of regulatory expertise.
The O'Neal Comprehensive Cancer Center is one of 51 NCI-designated comprehensive cancer centers in the United States and is the only one in Alabama and in the Deep South region. A comprehensive designation also means UAB Medicine patients have access to leading-edge treatments or clinical trials that they may not otherwise have at local community hospitals or smaller cancer centers. For many, an NCI designation can hold the key to survival. On campus and around Birmingham, the O'Neal Cancer Center is a significant part of our economic powerhouse. The O'Neal Cancer Center powers more than 400 scientists and physician-scientists, cares for 20,000 patients annually, and is home to more than 160 employees, plus all the physicians and clinical staff engaged in cancer patient care. The link to our website is: https://www.uab.edu/onealcancercenter/
General ResponsibilitiesTo prepare, submit, and assist with multiple levels of research documentation (i.e., IRB submissions, educational materials, reports, grant renewal reports, and study forms).
To maintain regulatory documentation, including consent forms, protocols, 1572s, CVs, licenses, investigator brochures, recruitment materials, safety reports, and submission forms.
To draft informed consents.
To prepare and maintain FDA applications for Investigational New Drugs (INDs) and Investigational Device Exemptions (IDEs).
To assist in drafting compliant advertisements.
To serve as resource person or act as consultant within area of regulatory expertise.
Performs other duties as assigned.
Annual Salary Range$47,665 - $77,455
Qualifications
Bachelor's degree in a related field and three (3) years of related experience required. Work experience may substitute for education requirement.
PreferencesAdvanced knowledge in regulatory matters related to clinical trials and retrospective IRBs.
Basic knowledge of clinicaltrials.gov, consenting, protocol review, adverse and serious adverse event reporting.
Ability to work independently, to make decisions, to interact with sponsors, regulatory authorities, and investigators.
Ability to communicate effectively with physicians, sponsors, and other collaborators.
UAB is an Equal Employment/Equal Educational Opportunity Institution dedicated to providing equal opportunities and equal access to all individuals regardless of race, color, religion, ethnic or national origin, sex (including pregnancy), genetic information, age, disability, and veteran's status. As required by Title IX, UAB prohibits sex discrimination in any education program or activity that it operates. Individuals may report concerns or questions to UAB's Assistant Vice President and Senior Title IX Coordinator. The Title IX notice of nondiscrimination is located at uab.edu/titleix.
Primary LocationUniversity
Job CategoryClinical Research
Employee StatusRegular
Shift : Day/1st Shift
Work Arrangement (final schedule to be determined by the department/hiring manager) : Remote/Hybrid Eligible
Get the full story on Breakroom
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The University of Alabama at Birmingham is the heartbeat of Birmingham and an integral medical leader in the Southeast. The Birmingham campus is within walking distance of some of the best parks, entertainment, and dining in the region. UAB's three regional campuses expand their academic reach and responsibilities in addition to educating physicians in rural and underserved areas of the state. UAB is experiencing major and sustained investment and growth, due both to its exceptional research faculty and its culture of collaboration. Through concerted and strategic investments in its clinical and research enterprise, UAB has undergone an amazing transformation in the past five years and has strengthened its status and reputation as a leader in medical training, biomedical discovery, innovation, and patient care.
Colleges, universities, and professional schools
10,000+ Employees
Birmingham, AL, US
1859
