Regulatory Affairs Assistant Location: Fully onsite Join our client's clinical research team as a Regulatory Affairs Assistant, where you'll play a key role in keeping studies compliant, organized ...
Regulatory Affairs Assistant Location: Fully onsite Join our client's clinical research team as a Regulatory Affairs Assistant, where you'll play a key role in keeping studies compliant, organized ...
Regulatory Affairs Project Manager
Branchburg, NJ · On-site +1
$93K - $172K/yr
The Opportunity * Assist in activities associated with regulatory approval of in vitro diagnostic medical devices in global markets. * Provide support to currently marketed products, e.g., review ...
Regulatory Affairs Project Manager
Branchburg, NJ · On-site +1
$93K - $172K/yr
The Opportunity * Assist in activities associated with regulatory approval of in vitro diagnostic medical devices in global markets. * Provide support to currently marketed products, e.g., review ...
Regulatory Affairs Project Manager
Branchburg, NJ · On-site
$93 - $173/hr
The Opportunity * Assist in activities associated with regulatory approval of in vitro diagnostic medical devices in global markets. * Provide support to currently marketed products, e.g., review ...
Regulatory Affairs Project Manager
Branchburg, NJ · On-site
$93 - $173/hr
The Opportunity * Assist in activities associated with regulatory approval of in vitro diagnostic medical devices in global markets. * Provide support to currently marketed products, e.g., review ...
Regulatory Affairs Project Manager
Branchburg, NJ · On-site
$93K - $172K/yr
The Opportunity * Assist in activities associated with regulatory approval of in vitro diagnostic medical devices in global markets. * Provide support to currently marketed products, e.g., review ...
Regulatory Affairs Project Manager
Branchburg, NJ · On-site
$93K - $172K/yr
The Opportunity * Assist in activities associated with regulatory approval of in vitro diagnostic medical devices in global markets. * Provide support to currently marketed products, e.g., review ...
Regulatory Affairs Project Manager
Branchburg, NJ · On-site
$93 - $173/hr
The Opportunity Assist in activities associated with regulatory approval of in vitro diagnostic medical devices in global markets. Provide support to currently marketed products, e.g., review ...
Regulatory Affairs Project Manager
Branchburg, NJ · On-site
$93 - $173/hr
The Opportunity Assist in activities associated with regulatory approval of in vitro diagnostic medical devices in global markets. Provide support to currently marketed products, e.g., review ...
Review and Approve Chinese language artwork, ensure compliance with China cosmetic regulations * Assist with regulatory documentation and technical assistance to support pre-market registrations
Review and Approve Chinese language artwork, ensure compliance with China cosmetic regulations * Assist with regulatory documentation and technical assistance to support pre-market registrations
Review and Approve Chinese language artwork, ensure compliance with China cosmetic regulations * Assist with regulatory documentation and technical assistance to support pre-market registrations
Review and Approve Chinese language artwork, ensure compliance with China cosmetic regulations * Assist with regulatory documentation and technical assistance to support pre-market registrations
Manager, Regulatory Affairs - China
Jersey City, NJ · On-site
$100 - $140/hr
Review and Approve Chinese language artwork, ensure compliance with China cosmetic regulations * Assist with regulatory documentation and technical assistance to support pre-market registrations
Manager, Regulatory Affairs - China
Jersey City, NJ · On-site
$100 - $140/hr
Review and Approve Chinese language artwork, ensure compliance with China cosmetic regulations * Assist with regulatory documentation and technical assistance to support pre-market registrations
Review and Approve Chinese language artwork, ensure compliance with China cosmetic regulations * Assist with regulatory documentation and technical assistance to support pre-market registrations
Review and Approve Chinese language artwork, ensure compliance with China cosmetic regulations * Assist with regulatory documentation and technical assistance to support pre-market registrations
Manager, Regulatory Affairs - China
Jersey City, NJ · On-site
$100 - $140/hr
Review and Approve Chinese language artwork, ensure compliance with China cosmetic regulations * Assist with regulatory documentation and technical assistance to support pre‑market registrations
Manager, Regulatory Affairs - China
Jersey City, NJ · On-site
$100 - $140/hr
Review and Approve Chinese language artwork, ensure compliance with China cosmetic regulations * Assist with regulatory documentation and technical assistance to support pre‑market registrations
Regulatory Specialist
$28.36 - $42.20/hr
Along with the entire Regulatory team, assist with ourHACCP plan and communicate changes with appropriate parties. * Collaborate with all departments to implement best practices and execute ...
Regulatory Specialist
$28.36 - $42.20/hr
Along with the entire Regulatory team, assist with ourHACCP plan and communicate changes with appropriate parties. * Collaborate with all departments to implement best practices and execute ...
Regulatory Specialist
Carteret, NJ · On-site
$28.36 - $42.20/hr
Along with the entire Regulatory team, assist with ourHACCP plan and communicate changes with appropriate parties. * Collaborate with all departments to implement best practices and execute ...
New
Regulatory Specialist
Carteret, NJ · On-site
$28.36 - $42.20/hr
Along with the entire Regulatory team, assist with ourHACCP plan and communicate changes with appropriate parties. * Collaborate with all departments to implement best practices and execute ...
New
The Assistant Vice President (AVP), Capital & Regulatory Reporting is responsible for supporting the preparation, review, and governance of applicable U.S. and international regulatory capital and ...
The Assistant Vice President (AVP), Capital & Regulatory Reporting is responsible for supporting the preparation, review, and governance of applicable U.S. and international regulatory capital and ...
Regulatory Reporting AVP - Capital & Regulatory Reporting
Jersey City, NJ · On-site
$87 - $147/hr
The Assistant Vice President (AVP), Capital & Regulatory Reporting is responsible for supporting the preparation, review, and governance of applicable U.S. and international regulatory capital and ...
New
Regulatory Reporting AVP - Capital & Regulatory Reporting
Jersey City, NJ · On-site
$87 - $147/hr
The Assistant Vice President (AVP), Capital & Regulatory Reporting is responsible for supporting the preparation, review, and governance of applicable U.S. and international regulatory capital and ...
New
Regulatory Reporting AVP - Capital & Regulatory Reporting
Jersey City, NJ · On-site
$87 - $147/hr
The Assistant Vice President (AVP), Capital & Regulatory Reporting is responsible for supporting the preparation, review, and governance of applicable U.S. and international regulatory capital and ...
New
Regulatory Reporting AVP - Capital & Regulatory Reporting
Jersey City, NJ · On-site
$87 - $147/hr
The Assistant Vice President (AVP), Capital & Regulatory Reporting is responsible for supporting the preparation, review, and governance of applicable U.S. and international regulatory capital and ...
New
Interim, Specialist, Regulatory
New York, NY · Remote
$60K - $80K/yr
Beauty products * Assist with monitoring new regulations and amendments; participate in trade association committees. Requirements: * 1-3 years' experience in the cosmetic industry in a Regulatory ...
Quick apply
Interim, Specialist, Regulatory
New York, NY · Remote
$60K - $80K/yr
Beauty products * Assist with monitoring new regulations and amendments; participate in trade association committees. Requirements: * 1-3 years' experience in the cosmetic industry in a Regulatory ...
Interim, Specialist, Regulatory
New York, NY · Hybrid
$60K - $80K/yr
Beauty products * Assist with monitoring new regulations and amendments; participate in trade association committees. Requirements: * 1-3 years' experience in the cosmetic industry in a Regulatory ...
Interim, Specialist, Regulatory
New York, NY · Hybrid
$60K - $80K/yr
Beauty products * Assist with monitoring new regulations and amendments; participate in trade association committees. Requirements: * 1-3 years' experience in the cosmetic industry in a Regulatory ...
Interim, Specialist, Regulatory
New York, NY · Hybrid
$60K - $80K/yr
Beauty products * Assist with monitoring new regulations and amendments; participate in trade association committees. Requirements: * 1-3 years' experience in the cosmetic industry in a Regulatory ...
Interim, Specialist, Regulatory
New York, NY · Hybrid
$60K - $80K/yr
Beauty products * Assist with monitoring new regulations and amendments; participate in trade association committees. Requirements: * 1-3 years' experience in the cosmetic industry in a Regulatory ...
Regulatory Affairs Associate
Staten Island, NY · On-site
$20 - $28/hr
The Regulatory Affairs Assistant supports efforts to ensure regulatory submission targets are met. Completes all duties under the direction of the Regulatory Manager or Site Director. In executing ...
Quick apply
Regulatory Affairs Associate
Staten Island, NY · On-site
$20 - $28/hr
The Regulatory Affairs Assistant supports efforts to ensure regulatory submission targets are met. Completes all duties under the direction of the Regulatory Manager or Site Director. In executing ...
Regulatory Document Analyst
New York, NY · On-site
$75K - $85K/yr
You'll help ensure our products meet regulatory and customer compliance requirements by managing ... agencies Assist with compiling and submitting documentation for retailer compliance portals ...
Regulatory Document Analyst
New York, NY · On-site
$75K - $85K/yr
You'll help ensure our products meet regulatory and customer compliance requirements by managing ... agencies Assist with compiling and submitting documentation for retailer compliance portals ...
Regulatory Assistant information
See Basking Ridge, NJ salary details
$41.7K is the 25th percentile. Wages below this are outliers.
$35K - $42.6K
28% of jobs
The median wage is $48K / yr.
$42.6K - $50.1K
30% of jobs
$56.5K is the 75th percentile. Wages above this are outliers.
$50.1K - $57.7K
20% of jobs
$57.7K - $65.2K
0% of jobs
$65.2K - $72.7K
0% of jobs
$72.7K - $80.3K
7% of jobs
$80.3K - $87.8K
1% of jobs
$87.8K - $95.4K
0% of jobs
$95.4K - $102.9K
0% of jobs
$102.9K - $110.5K
6% of jobs
$110.5K - $118K
7% of jobs
$35K
$60.8K
$118K
How much do regulatory assistant jobs pay per year?
What is a regulatory assistant?
A regulatory assistant has a crucial job in any research lab, seeing that every step of a clinical study follows regulations. As a regulatory assistant, your duties include keeping up to date with regulations and ensuring that everyone in the lab follows the correct procedures. You may also collect and prepare lab samples and maintain various documents. You provide a valuable service, serving as a liaison between a laboratory and regulatory agencies. Qualifications typically include a bachelor’s degree in a relevant scientific field, although a master’s degree is sometimes preferred. To be successful in this career, you need strong communication and time-management skills, attention to detail, and prior office experience working with a team.
What are the key skills and qualifications needed to thrive as a regulatory assistant, and why are they important?
What are some common challenges faced by regulatory assistants during the document submission process?
What is the difference between Regulatory Assistant vs Compliance Coordinator?
| Aspect | Regulatory Assistant | Compliance Coordinator |
|---|---|---|
| Required Credentials | Associate's degree, certifications like RAC or RAPS often preferred | Bachelor's degree, certifications like RAC or RAPS common |
| Work Environment | Office setting, supporting regulatory teams in healthcare, pharmaceuticals, or medical devices | Office setting, overseeing compliance programs in similar industries |
| Employer & Industry Usage | Used by pharmaceutical, biotech, medical device companies | Used by healthcare, pharmaceutical, and medical device firms |
| Search & Comparison Intent | Often compared for entry-level regulatory roles | Related to regulatory roles but with broader compliance responsibilities |
The Regulatory Assistant primarily supports regulatory teams by preparing documentation and ensuring compliance with regulations. The Compliance Coordinator has a broader role, overseeing compliance programs and policies. While both roles require similar credentials and work in related industries, the Compliance Coordinator typically has more responsibility for overall compliance management.
Is regulatory assistant high paying?
What are the most commonly searched types of Regulatory jobs in Basking Ridge, NJ?
The most popular types of Regulatory jobs in Basking Ridge, NJ are:
What cities near Basking Ridge, NJ are hiring for Regulatory Assistant jobs?
Cities near Basking Ridge, NJ with the most Regulatory Assistant job openings:

Other
Posted 13 days ago
Job description
Regulatory Affairs Assistant
Location: Fully onsite
Join our client's clinical research team as a Regulatory Affairs Assistant, where you'll play a key role in keeping studies compliant, organized, and audit-ready. This is a fully onsite position and a great opportunity for a detail-oriented professional to grow within a fast-paced research environment - no prior clinical research experience required, just a strong work ethic and a sharp eye for accuracy.
What You'll Do
A general understanding of GCP/ICH guidelines is expected. Day to day, you will:
- Collect and prepare regulatory documents for submission to the sponsor and IRB
- Maintain current regulatory documents, including CVs, licenses, and required training records
- Set up the electronic Investigator Site File (ISF) for all awarded studies
- Obtain signatures on regulatory documents as needed
- Keep study logs up to date, such as Screening and Enrollment Logs and Training Logs
- File study-related correspondence (sponsor, IRB, etc.) in the Investigator Site File
- Support the resolution of regulatory items identified during monitoring visits
- Maintain current training on applicable SOPs/WIs, GCP, and related requirements
- Archive study documents following study closure
What You'll Bring
Education and Experience
- High school diploma or equivalent; two-year degree preferred
- Clinical research experience preferred but not required
Requirements
- Working knowledge of medical terminology and the clinical research process
- Strong attention to detail
- Solid organizational skills
- Strong computer skills, including proficiency across all Microsoft Office applications