Research Regulatory Assistant
$41K - $68K/yr
This position will be assisting in the overseeing of clinical research regulatory requirements for the department. The Regulatory Assistant will provide support in managing clinical trials for the ...
$41K - $68K/yr
This position will be assisting in the overseeing of clinical research regulatory requirements for the department. The Regulatory Assistant will provide support in managing clinical trials for the ...
$41K - $68K/yr
This position will be assisting in the overseeing of clinical research regulatory requirements for the department. The Regulatory Assistant will provide support in managing clinical trials for the ...
Providence, RI · On-site
$41K - $68K/yr
This position will be assisting in the overseeing of clinical research regulatory requirements for the department. The Regulatory Assistant will provide support in managing clinical trials for the ...
Providence, RI · On-site
$41K - $68K/yr
This position will be assisting in the overseeing of clinical research regulatory requirements for the department. The Regulatory Assistant will provide support in managing clinical trials for the ...
$41K - $68K/yr
This position will be assisting in the overseeing of clinical research regulatory requirements for the department. The Regulatory Assistant will provide support in managing clinical trials for the ...
$41K - $68K/yr
This position will be assisting in the overseeing of clinical research regulatory requirements for the department. The Regulatory Assistant will provide support in managing clinical trials for the ...
$41K - $68K/yr
This position will be assisting in the overseeing of clinical research regulatory requirements for the department. The Regulatory Assistant will provide support in managing clinical trials for the ...
$41K - $68K/yr
This position will be assisting in the overseeing of clinical research regulatory requirements for the department. The Regulatory Assistant will provide support in managing clinical trials for the ...
$41K - $68K/yr
This position will be assisting in the overseeing of clinical research regulatory requirements for the department. The Regulatory Assistant will provide support in managing clinical trials for the ...
$41K - $68K/yr
This position will be assisting in the overseeing of clinical research regulatory requirements for the department. The Regulatory Assistant will provide support in managing clinical trials for the ...
The Clinical Research Regulatory Specialist will collaborate with OneR operations team and ... * Assist in the review of clinical trial protocols, informed consent forms, and other study ...
The Clinical Research Regulatory Specialist will collaborate with OneR operations team and ... * Assist in the review of clinical trial protocols, informed consent forms, and other study ...
Cortland, NY · On-site
$22 - $30/hr
The Clinical Research Regulatory Coordinator is responsible for preparing and maintaining ... Maintain document version control. * Assist sites with regulatory filing and document management ...
Quick apply
Cortland, NY · On-site
$22 - $30/hr
The Clinical Research Regulatory Coordinator is responsible for preparing and maintaining ... Maintain document version control. * Assist sites with regulatory filing and document management ...
Horseheads, NY · On-site
$22 - $30/hr
The Clinical Research Regulatory Coordinator is responsible for preparing and maintaining ... Maintain document version control. * Assist sites with regulatory filing and document management ...
Quick apply
Horseheads, NY · On-site
$22 - $30/hr
The Clinical Research Regulatory Coordinator is responsible for preparing and maintaining ... Maintain document version control. * Assist sites with regulatory filing and document management ...
... regulatory (eRegulatory) platform ... Reporting to the Assistant Director of Clinical Research Operations , this individual will serve as ...
... regulatory (eRegulatory) platform ... Reporting to the Assistant Director of Clinical Research Operations , this individual will serve as ...
... regulatory (eRegulatory) platform ... Reporting to the Assistant Director of Clinical Research Operations , this individual will serve as ...
... regulatory (eRegulatory) platform ... Reporting to the Assistant Director of Clinical Research Operations , this individual will serve as ...
Job Summary The Clinical Research Regulatory Specialist supports clinical research by developing protocol-specific documents and reports. This role focuses on developing, submitting, maintaining ...
Job Summary The Clinical Research Regulatory Specialist supports clinical research by developing protocol-specific documents and reports. This role focuses on developing, submitting, maintaining ...
... regulatory (eRegulatory) platform ... Reporting to the Assistant Director of Clinical Research Operations , this individual will serve as ...
... regulatory (eRegulatory) platform ... Reporting to the Assistant Director of Clinical Research Operations , this individual will serve as ...
Job Summary The Clinical Research Regulatory Specialist supports clinical research by developing protocol-specific documents and reports. This role focuses on developing, submitting, maintaining ...
Job Summary The Clinical Research Regulatory Specialist supports clinical research by developing protocol-specific documents and reports. This role focuses on developing, submitting, maintaining ...
... regulatory (eRegulatory) platform ... Reporting to the Assistant Director of Clinical Research Operations , this individual will serve as ...
... regulatory (eRegulatory) platform ... Reporting to the Assistant Director of Clinical Research Operations , this individual will serve as ...
$75K - $81K/yr
Experience in clinical research compliance, regulatory research and/or operations in the academic or private sector. Experience with submissions to the Institutional Review Board and/or the Federal ...
$75K - $81K/yr
Experience in clinical research compliance, regulatory research and/or operations in the academic or private sector. Experience with submissions to the Institutional Review Board and/or the Federal ...
Los Angeles, CA · On-site
$75K - $81K/yr
Experience in clinical research compliance, regulatory research and/or operations in the academic or private sector. Experience with submissions to the Institutional Review Board and/or the Federal ...
Los Angeles, CA · On-site
$75K - $81K/yr
Experience in clinical research compliance, regulatory research and/or operations in the academic or private sector. Experience with submissions to the Institutional Review Board and/or the Federal ...
$75K - $81K/yr
Experience in clinical research compliance, regulatory research and/or operations in the academic or private sector. Experience with submissions to the Institutional Review Board and/or the Federal ...
$75K - $81K/yr
Experience in clinical research compliance, regulatory research and/or operations in the academic or private sector. Experience with submissions to the Institutional Review Board and/or the Federal ...
Brandon, FL · On-site
$22 - $29.25/hr
The Clinical Research Regulatory Coordinator is responsible for preparing and maintaining ... • Assist sites with regulatory filing and document management activities. • Support ...
Brandon, FL · On-site
$22 - $29.25/hr
The Clinical Research Regulatory Coordinator is responsible for preparing and maintaining ... • Assist sites with regulatory filing and document management activities. • Support ...
Brandon, FL · On-site
$22 - $29.25/hr
The Clinical Research Regulatory Coordinator is responsible for preparing and maintaining ... · Assist sites with regulatory filing and document management activities. · Support ...
Quick apply
Brandon, FL · On-site
$22 - $29.25/hr
The Clinical Research Regulatory Coordinator is responsible for preparing and maintaining ... · Assist sites with regulatory filing and document management activities. · Support ...
The Clinical Research Regulatory Coordinator ensures regulatory compliance and accurate documentation for all clinical research studies conducted at Cooper University Health Care. * This role ...
The Clinical Research Regulatory Coordinator ensures regulatory compliance and accurate documentation for all clinical research studies conducted at Cooper University Health Care. * This role ...
$8.17 - $11.63
7% of jobs
$11.63 - $15.08
2% of jobs
$17.07 is the 25th percentile. Wages below this are outliers.
$15.08 - $18.53
27% of jobs
The median wage is $20.33 / hr.
$18.53 - $21.98
26% of jobs
$24.75 is the 75th percentile. Wages above this are outliers.
$21.98 - $25.44
16% of jobs
$25.44 - $28.89
9% of jobs
$28.89 - $32.34
7% of jobs
$32.34 - $35.80
4% of jobs
$35.80 - $39.25
1% of jobs
$39.25 - $42.70
0% of jobs
$42.70 - $46.15
0% of jobs
$8
$22
$46
| Aspect | Clinical Research Regulatory Assistant | Clinical Research Coordinator |
|---|---|---|
| Credentials | Typically requires a bachelor's degree in health, life sciences, or related field; certifications like CCRP are a plus | Requires a bachelor's degree; certifications like CCRP or RAC are common |
| Work Environment | Supports regulatory documentation, compliance, and submissions; often works in offices or labs | Manages study participants, coordinates activities, and oversees daily trial operations |
| Employer & Industry Usage | Used by pharmaceutical companies, CROs, and research institutions for regulatory tasks | Employed by hospitals, research centers, and clinics to oversee clinical trial processes |
While both roles support clinical research, the Clinical Research Regulatory Assistant focuses on regulatory compliance and documentation, whereas the Clinical Research Coordinator manages study operations and participant interactions. Understanding these differences helps in choosing the right career path or job search focus.
Cities with the most Clinical Research Regulatory Assistant job openings:
The most popular types of Clinical Research Regulatory jobs are:
States with the most job openings for Clinical Research Regulatory Assistant jobs include:
The top searched job categories for Clinical Research Regulatory Assistant jobs are:

$41K - $68K/yr
Full-time
Posted 23 days ago
6.8
Based on 71 frontline employees who took The Breakroom Quiz
493rd of 887 rated healthcare providers
SUMMARY The Regulatory Assistant performs multiple tasks in order to meet compliance requirements in research. This position will be assisting in the overseeing of clinical research regulatory requirements for the department. The Regulatory Assistant will provide support in managing clinical trials for the department.
The Regulatory Assistant supports the department and clinical studies through the regulatory portion of the trial submission process to maintaining the regulatory integrity of assigned clinical trials from approval to closure. The Regulatory Assistant works closely with other Regulatory Assistants and Regulatory Coordinators within the department. Brown University Health employees are expected to successfully role model the organization's values of Compassion, Accountability, Respect, and Excellence as these values guide our everyday actions with patients, customers, and one another.
In addition to our values, all employees are expected to demonstrate the core Success Factors which tell us how we work together and how we get things done. The core Success Factors include: Instill Trust and Value Differences Patient and Community Focus and Collaborate RESPONSIBILITIES The Regulatory Assistant supports clinical trials in an administrative manner and is responsible for the following duties: Assist with the preparation and/or collection of study related research required regulatory documents, including but not limited to: CVs MLs Financial Disclosure Forms Conflict of Interest Forms FDA 1572 Delegation of Authority/Staff Signature Logs May collect signatures to ensure accuracy of study documents Receives and processes clinical trial external safety reports, including SUSARs May process and file IRB and RDC approvals; may update the Clinical Trial Management System May complete minor revisions to clinical trials, such as personnel updates or continuing reviews May assist with the preparation and set-up of sponsor visits, such as Monitoring Visits, Site Initiation Visits, and Close-Out Visits Liaises with regulatory staff, sponsors, investigators, and research team members Participates in Study Initiation Visits and Interim Monitoring Visits Performs other duties as assigned MINIMUM QUALIFICATIONS BASIC KNOWLEDGE: Bachelor's degree in Applied or Life Sciences or related area, including courses in research methodologies and microcomputer systems. In lieu of a bachelor's degree, an additional 2-3 years of experience may be substituted.
Knowledge of theory and techniques of research methodology Must possess the following skills: Detail-oriented and excellent organizational skills Strong self-starter Interpersonal skills Team-oriented Excellent oral and written communication skills Proficient in Microsoft Office and in various database applications EXPERIENCE: 6 months - 1 year in direct clinical trial administration experience or relevant administrative experience preferred but not required. The Regulatory Assistant should develop a general understanding of compliance requirements with federal, state, and/or local programmatic regulations within three months of employment. WORK ENVIRONMENT AND PHYSICAL REQUIREMENTS This position is a sedentary position.
One must be able to transport paperwork to another building (sometimes up to 10 lbs.) at one time. Bending and stooping may also be requirements for filing of paperwork. Standing to copy may also be required
INDEPENDENT ACTION This position requires a quick thinker, who can independently make basic and sometimes complex decisions pertaining to the completion and transmission of required regulatory documentation to internal departments, as well as external agencies, including, but not limited to study sponsors, local and federal agencies. This person should also be able to work with outside monitors and work independently. He/she should be able to answer inquiries related to regulatory issues, and if not known, communicate with the correct person to determine the answer.
SUPERVISORY RESPONSIBILITY None Pay Range $41,537.60 - $68,556.80 Location Rhode Island Hospital - 593 Eddy Street Providence, Rhode Island 02903 Work Type M-F 8:00am - 4:30pm Work Shift Day Daily Hours 8 hours Driving Required No Brown University Health is committed to providing equal employment opportunities and maintaining a work environment free from all forms of unlawful discrimination and harassment. Apply
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