... submissions and renewals, regulatory compliance, data management, manuscript development ... Experience with scientific publishing, grant preparation, and regulatory compliance is preferred.
... submissions and renewals, regulatory compliance, data management, manuscript development ... Experience with scientific publishing, grant preparation, and regulatory compliance is preferred.
Regulatory Affairs Manager
Santa Ana, CA · On-site
$38 - $48/hr
Santa Ana, California, Orange County Schedule: Part-time, approximately 10 hours per week Work ... Lead or support FDA submissions and regulatory pathways, including New Dietary Ingredient ...
Quick apply
Regulatory Affairs Manager
Santa Ana, CA · On-site
$38 - $48/hr
Santa Ana, California, Orange County Schedule: Part-time, approximately 10 hours per week Work ... Lead or support FDA submissions and regulatory pathways, including New Dietary Ingredient ...
Clinical Affairs Manager (Part-Time)
$135 - $175/hr
About the Job As the Clinical Affairs Manager (Part-Time) , you will lead clinical affairs and ... Oversee clinical data collection and analysis for regulatory submissions * Hospital Partnerships ...
Clinical Affairs Manager (Part-Time)
$135 - $175/hr
About the Job As the Clinical Affairs Manager (Part-Time) , you will lead clinical affairs and ... Oversee clinical data collection and analysis for regulatory submissions * Hospital Partnerships ...
Part time (PRN) SDS Author (Remote)
Minneapolis, MN · Remote
$35 - $40/hr
Provide SDS authoring and regulatory compliance support as it applies to our client's products. Research, author, and review chemical hazard assessments, hazard profiles, product labels, safety data ...
Part time (PRN) SDS Author (Remote)
Minneapolis, MN · Remote
$35 - $40/hr
Provide SDS authoring and regulatory compliance support as it applies to our client's products. Research, author, and review chemical hazard assessments, hazard profiles, product labels, safety data ...
Biocon - Introduction to US FDA and European Laws and Regulations (Adjunct), Henry E. Riggs School o
Claremont, CA · On-site
$2.5K - $15K/mo
Emphasis will be placed on regulatory interactions - submissions, other communications and ... This is a part-time, exempt, adjunct faculty position and is not eligible for benefits. Schedules ...
Biocon - Introduction to US FDA and European Laws and Regulations (Adjunct), Henry E. Riggs School o
Claremont, CA · On-site
$2.5K - $15K/mo
Emphasis will be placed on regulatory interactions - submissions, other communications and ... This is a part-time, exempt, adjunct faculty position and is not eligible for benefits. Schedules ...
Document Specialist (Part-TIme)
$19 - $20/hr
Leading Pharmaceutical Manufacturer Requires a Part-Time 1st Shift Document Specialist at their ... regulatory submissions, standard operating procedures (SOPs), clinical trial documents, and other ...
Quick apply
Document Specialist (Part-TIme)
$19 - $20/hr
Leading Pharmaceutical Manufacturer Requires a Part-Time 1st Shift Document Specialist at their ... regulatory submissions, standard operating procedures (SOPs), clinical trial documents, and other ...
Part Time Clinical Research Coordinator
Monroeville, PA · On-site
$53K - $58K/yr
Job Type Part-time Description The Clinical Research Coordinator (CRC) at SerenaGroup plays a ... Familiarity with clinical trial start-up and regulatory submissions Salary Description $53,000-$58 ...
Part Time Clinical Research Coordinator
Monroeville, PA · On-site
$53K - $58K/yr
Job Type Part-time Description The Clinical Research Coordinator (CRC) at SerenaGroup plays a ... Familiarity with clinical trial start-up and regulatory submissions Salary Description $53,000-$58 ...
Director of Clinical Research (PT/FT)
Manhattan, NY · On-site
$150K - $228K/yr
... publish the work that makes precision mental health real. We're running clinical trials running ... You'll manage IRB submissions and regulatory compliance across our multi-site trial portfolio. And ...
Director of Clinical Research (PT/FT)
Manhattan, NY · On-site
$150K - $228K/yr
... publish the work that makes precision mental health real. We're running clinical trials running ... You'll manage IRB submissions and regulatory compliance across our multi-site trial portfolio. And ...
Clinical Research Associate-Regulatory
$22.83 - $34.51/hr
Varies (United States of America) Hours: 24 Salary range: $22.83 - $34.51 Schedule: Part Time Shift ... submission to the Eisenhower Human Research Protections Program (Eisenhower Medical Center ...
Clinical Research Associate-Regulatory
$22.83 - $34.51/hr
Varies (United States of America) Hours: 24 Salary range: $22.83 - $34.51 Schedule: Part Time Shift ... submission to the Eisenhower Human Research Protections Program (Eisenhower Medical Center ...
Maintaining calendar to ensure timely submission of letters of inquiry, proposal deadlines, and ... Personal computer including financial, accounting, payroll, data base, scheduling, publishing ...
Quick apply
Maintaining calendar to ensure timely submission of letters of inquiry, proposal deadlines, and ... Personal computer including financial, accounting, payroll, data base, scheduling, publishing ...
(Part-Time) Grant Coordinator
Brighton, MI · On-site
$25 - $39/hr
Maintaining calendar to ensure timely submission of letters of inquiry, proposal deadlines, and ... Personal computer including financial, accounting, payroll, data base, scheduling, publishing ...
(Part-Time) Grant Coordinator
Brighton, MI · On-site
$25 - $39/hr
Maintaining calendar to ensure timely submission of letters of inquiry, proposal deadlines, and ... Personal computer including financial, accounting, payroll, data base, scheduling, publishing ...
Receptionist / Recreation Service Aide
Doral, FL · On-site
$15.76/hr
City of Doral, FL Job Type: Part-Time Job Number: 07272026 Department: Parks & Recreation Opening ... Enforces safety and other park rules and regulations; administers first aid as required. * Coaches ...
Receptionist / Recreation Service Aide
Doral, FL · On-site
$15.76/hr
City of Doral, FL Job Type: Part-Time Job Number: 07272026 Department: Parks & Recreation Opening ... Enforces safety and other park rules and regulations; administers first aid as required. * Coaches ...
... and other regulatory submissions, subject recruitment, trained research nurses and statistical ... By October 1 of each year, institutions must publish and distribute their Annual Campus Security ...
... and other regulatory submissions, subject recruitment, trained research nurses and statistical ... By October 1 of each year, institutions must publish and distribute their Annual Campus Security ...
Part-time Entry Level Accountant
Fort Lauderdale, FL · On-site
$25 - $30/hr
Review work for accuracy and completeness before submission; flag discrepancies * Support ... publishing, and other industries with annual budgets ranging from $175,000 to $6 million.
Quick apply
Part-time Entry Level Accountant
Fort Lauderdale, FL · On-site
$25 - $30/hr
Review work for accuracy and completeness before submission; flag discrepancies * Support ... publishing, and other industries with annual budgets ranging from $175,000 to $6 million.
Part-time Entry Level Accountant
Fort Lauderdale, FL · On-site
$25 - $30/hr
Review work for accuracy and completeness before submission; flag discrepancies * Support ... publishing, and other industries with annual budgets ranging from $175,000 to $6 million.
Quick apply
Part-time Entry Level Accountant
Fort Lauderdale, FL · On-site
$25 - $30/hr
Review work for accuracy and completeness before submission; flag discrepancies * Support ... publishing, and other industries with annual budgets ranging from $175,000 to $6 million.
Research Intern (Part-Time) - CalHeart
Beverly Hills, CA · On-site
$25 - $27.70/hr
... regulatory submissions and other study-related administrative activities. • Coordinate with internal and external research collaborators, including the Biomanufacturing team. • Perform other ...
Research Intern (Part-Time) - CalHeart
Beverly Hills, CA · On-site
$25 - $27.70/hr
... regulatory submissions and other study-related administrative activities. • Coordinate with internal and external research collaborators, including the Biomanufacturing team. • Perform other ...
Part Time - Athletics - Outside Events Support
Reading, PA · On-site
$14.50 - $19.25/hr
Enforce rules and regulations of athletic/recreational facilities and/or activities. * Monitor ... Penn State publishes a combined Annual Security and Annual Fire Safety Report (ASR). The ASR ...
Part Time - Athletics - Outside Events Support
Reading, PA · On-site
$14.50 - $19.25/hr
Enforce rules and regulations of athletic/recreational facilities and/or activities. * Monitor ... Penn State publishes a combined Annual Security and Annual Fire Safety Report (ASR). The ASR ...
... submission and support future grant proposals on this topic. BACKGROUND CHECKS/CLEARANCES ... Penn State publishes a combined Annual Security and Annual Fire Safety Report (ASR). The ASR ...
... submission and support future grant proposals on this topic. BACKGROUND CHECKS/CLEARANCES ... Penn State publishes a combined Annual Security and Annual Fire Safety Report (ASR). The ASR ...
$19 - $26/hr
... submission and support future grant proposals on this topic. BACKGROUND CHECKS/CLEARANCES ... Penn State publishes a combined Annual Security and Annual Fire Safety Report (ASR). The ASR ...
$19 - $26/hr
... submission and support future grant proposals on this topic. BACKGROUND CHECKS/CLEARANCES ... Penn State publishes a combined Annual Security and Annual Fire Safety Report (ASR). The ASR ...
$17.75 - $23.75/hr
Provide assistance to administrative team members in the preparation, processing, and submission of ... Penn State publishes a combined Annual Security and Annual Fire Safety Report (ASR). The ASR ...
$17.75 - $23.75/hr
Provide assistance to administrative team members in the preparation, processing, and submission of ... Penn State publishes a combined Annual Security and Annual Fire Safety Report (ASR). The ASR ...
Part Time Regulatory Submission Publisher information
See salary details
$19.04 is the 25th percentile. Wages below this are outliers.
$15.63 - $27.45
86% of jobs
$27.45 - $39.27
5% of jobs
$39.27 - $51.09
0% of jobs
$51.09 - $62.92
5% of jobs
$62.92 - $74.74
1% of jobs
$74.74 - $86.56
2% of jobs
$86.56 - $98.38
0% of jobs
$98.38 - $110.21
0% of jobs
$110.21 - $122.03
0% of jobs
$122.03 - $133.85
0% of jobs
$133.85 - $145.67
0% of jobs
$15
$34
$145
How much do part time regulatory submission publisher jobs pay per hour?
What is the difference between Part Time Regulatory Submission Publisher vs Part Time Regulatory Affairs Associate?
| Aspect | Part Time Regulatory Submission Publisher | Part Time Regulatory Affairs Associate |
|---|---|---|
| Credentials | Typically requires a degree in life sciences or related field, familiarity with submission software | Requires similar degrees, often with additional knowledge of regulatory processes |
| Work Environment | Primarily office-based, focused on document preparation and submission | Office-based, involved in broader regulatory activities and communication |
| Industry Usage | Common in pharmaceutical and biotech companies for submission tasks | Used across pharmaceutical, biotech, and medical device industries for regulatory support |
While both roles require knowledge of regulatory documentation, the Part Time Regulatory Submission Publisher mainly focuses on preparing and submitting documents, whereas the Part Time Regulatory Affairs Associate has broader responsibilities in regulatory strategy and compliance support.

Temple University rating
9.0
Based on 22 frontline employees who took The Breakroom Quiz
26th of 614 rated colleges and universities
Job description
Position Summary:
The Research Coordinator, at the Lewis Katz School of Medicine's Center for Asian Health (CAH), will work on several large-scale clinical, translational, and community-based research projects with clinical principal investigators and senior team staff at the CAH. This person will serve as the primary coordinator for multiple concurrent research projects, managing project coordination, project strategy development, study implementation, Institutional Review Board (IRB) submissions and renewals, regulatory compliance, data management, manuscript development, publication submission, grant preparation, and research timelines.
The Research Coordinator will proactively monitor project progress, identify barriers to completion, coordinate investigators, collaborators, trainees, and research personnel, and facilitate the timely completion of manuscripts, presentations, grant applications, regulatory submissions, and other scholarly activities. This individual will work with a high degree of independence while ensuring that research projects remain organized, productive, and aligned with strategic priorities and publication goals.
Job Details:
* This is a grant funded position
Required Education and Experience:
* Bachelor's degree in Health Sciences, Psychology, Public Health, Epidemiology, Biostatistics, Biology, or a related field required and at least two years' related research coordination experience. An equivalent combination of education and experience may be considered.
* Demonstrated knowledge of clinical and translational research methodology, study design, regulatory requirements, and research ethics is required.
Preferred Education and Experience:
* Master's degree in Public Health, Epidemiology, Clinical Research, Biostatistics, or a related discipline.
Required Skills and Abilities:
* Demonstrated computer skills and proficiency with the Microsoft Office Suite, including spreadsheet, database, and presentation software programs.
* Demonstrated data management, statistical analysis, interpretation, and data visualization skills.
* Excellent scientific writing, editing, and communication skills.
* Demonstrated organizational, project coordination, and problem-solving skills.
* Demonstrated ability to independently coordinate multiple concurrent research projects while maintaining competing priorities and deadlines.
* Ability to proactively identify barriers to research progress, facilitate solutions, and maintain accountability for project milestones and deliverables.
* Excellent communication and interpersonal skills, along with the ability to interact with a diverse constituent population including faculty, trainees, clinicians, community partners, patients, funding agencies, and journal editors.
* Ability to work independently and as part of a multidisciplinary team.
* Ability to organize and prioritize the needs of multiple research endeavors.
* Ability to multitask and be detail-oriented in a dynamic work environment.
* Flexibility, resilience, initiative, and the ability to accomplish goals with minimal supervision.
* Patient-centered communication and relationship-building with the community
Preferred Skills and Abilities:
* Experience with scientific publishing, grant preparation, and regulatory compliance is preferred.
* Proficiency in a second language is preferred (both verbal and written).
* A strong statistical background with experience managing, analyzing, interpreting, and presenting research data using a variety of quantitative analytical methods is highly desirable. Experience using statistical software such as SPSS, SAS, R, Stata, or equivalent analytical programs is preferred.
* Experience with Institutional Review Board (IRB) submissions, research databases (e.g., REDCap), scientific writing, manuscript preparation, publication management, grant preparation, and project coordination is preferred.
Essential Duties:
Research Portfolio Management
* Work closely with the Principal Investigator to ensure that the research portfolio progresses efficiently and that scholarly goals are achieved on schedule.
* Maintain oversight of multiple concurrent research projects.
* Develop and update comprehensive project timelines and milestone trackers.
* Monitor progress toward manuscript, presentation, grant, and regulatory deadlines.
* Ensure research priorities remain aligned with the strategic goals of the Center.
Research Project Coordination
* Serve as the primary point of contact for assigned research projects.
* Coordinate activities among principal investigators, collaborators, trainees, students, statisticians, and research personnel.
* Develop and maintain project timelines, milestone trackers, and action plans.
* Monitor research progress and facilitate the timely completion of project deliverables.
* Coordinate meetings, prepare agendas, document action items, and communicate project updates.
Study Implementation
* Oversee the day-to-day implementation of active research studies and serves as a liaison between investigators, participants, clinical teams, and community partners.
* Coordinating participant recruitment, enrollment, and informed consent.
* Scheduling study visits and research activities.
* Coordinating community outreach, educational programs, and research interventions.
* Presenting project updates during research meetings.
* Maintaining study documentation and research records.
Regulatory Compliance
* Responsible for ensuring compliance with institutional, regulatory, and sponsor requirements throughout the lifecycle of each project.
* Preparing and submitting IRB applications, amendments, continuing reviews, and study closures.
* Maintaining regulatory documentation and study records.
* Monitoring compliance with institutional policies and sponsor requirements.
* Assisting with grant reporting and regulatory documentation.
Data Management and Statistical Analysis
* Oversees research data management activities and supports quantitative analyses necessary for scientific publication.
* Coordinating data collection, organization, quality assurance, and database management.
* Performing or coordinating statistical analyses using appropriate analytical methods.
* Preparing publication-quality tables, figures, and graphical data visualizations.
* Assisting investigators with interpretation and presentation of research findings.
Scientific Writing and Publication
* Supports all phases of scholarly dissemination.
* Conducting literature reviews.
* Drafting, editing, and reviewing manuscripts, abstracts, presentations, and reports.
* Coordinating manuscript development among multiple authors.
* Managing journal submissions and peer-review revisions.
* Communicating with journal editors and publishers throughout the publication process.
Grant Development
* Coordinating grant timelines and submission requirements.
* Preparing supporting documents and administrative materials.
* Assisting with investigator-initiated grant proposals and progress reports.
* Maintaining compliance with sponsor requirements.
Temple University is committed to a policy of equal opportunity for all in every aspect of its operations, including employment, service, and educational programs. The University has pledged not to discriminate on the basis of age, color, disability, marital status, national origin or ethnic origin, race, religion, sex (including pregnancy), sexual orientation, gender identity, genetic information or veteran status.
Compliance Statement: In the performance of their functions as detailed in the position description employees have an obligation to avoid ethical, legal, financial and other conflicts of interest to ensure that their actions and outside activities do not conflict with their primary employment responsibilities at the institution. Employees are also expected to understand and be in compliance with applicable laws, University and employment policies and regulations, including NCAA regulations for areas and departments which their essential functions cause them to interact.
Temple University's Annual Security and Fire Safety Report contains statistics, policies, and procedures related to campus safety. Go here to review: https://safety.temple.edu/reports-logs/annual-security-report
You may request a copy of the report by calling Temple University's Campus Safety Services at 215-204-7900.
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