Remote Duration: 6-Month Contract Experience: 5-6 Years Job Overview We are seeking a Regulatory ... Familiarity with eCTD publishing solutions; eCTD 4.0 experience is a plus. I am actively connecting ...
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Remote Duration: 6-Month Contract Experience: 5-6 Years Job Overview We are seeking a Regulatory ... Familiarity with eCTD publishing solutions; eCTD 4.0 experience is a plus. I am actively connecting ...
Remote Ectd Publisher information
See Basking Ridge, NJ salary details
$13.13 - $17.84
8% of jobs
$17.84 - $22.54
10% of jobs
$23.27 is the 25th percentile. Wages below this are outliers.
$22.54 - $27.25
51% of jobs
$30.78 is the 75th percentile. Wages above this are outliers.
$27.25 - $31.96
10% of jobs
$31.96 - $36.66
9% of jobs
$36.66 - $41.37
4% of jobs
$41.37 - $46.08
3% of jobs
$46.08 - $50.79
1% of jobs
$50.79 - $55.49
2% of jobs
$55.49 - $60.20
2% of jobs
$60.20 - $64.91
1% of jobs
$13
$30
$64
How much do remote ectd publisher jobs pay per hour?
As of Aug 13, 2026, the average hourly pay for remote ectd publisher in Basking Ridge, NJ is $30.82, according to ZipRecruiter salary data. Most workers in this role earn between $23.80 and $35.43 per hour, depending on experience, location, and employer.
What is a Remote eCTD Publisher?
A Remote eCTD Publisher is a professional responsible for preparing, compiling, and submitting electronic Common Technical Document (eCTD) submissions to regulatory agencies, such as the FDA or EMA, from a remote location. They ensure all documents are formatted correctly, validated, and compliant with regulatory requirements. Their work supports pharmaceutical and biotechnology companies in getting approvals for drugs, biologics, or medical devices. Remote eCTD Publishers use specialized software to manage submissions and often collaborate with regulatory affairs and document management teams virtually.
What are the key skills and qualifications needed to thrive as a Remote eCTD Publisher?
To thrive as a Remote eCTD Publisher, you need a solid understanding of regulatory submission standards, document management, and eCTD structure, typically supported by a degree in life sciences or a related field. Familiarity with eCTD publishing software (like Lorenz docuBridge or Extedo), Adobe Acrobat, and regulatory portals is essential, and certifications in regulatory affairs are highly valued. Exceptional attention to detail, organizational skills, and the ability to communicate clearly with cross-functional teams are important soft skills. These competencies ensure accurate, compliant, and timely submissions to regulatory authorities, which are critical for drug approval processes.
Can you work in publishing remotely?
Remote Ectd Publisher roles are often available, allowing professionals to work from home or any location with internet access. These positions typically require familiarity with publishing software, document management, and attention to detail, and may involve flexible schedules. Remote work in publishing is common in companies that utilize digital tools and cloud-based collaboration platforms.
What is the difference between Remote Ectd Publisher vs Remote Regulatory Affairs Associate?
| Aspect | Remote Ectd Publisher | Remote Regulatory Affairs Associate |
|---|---|---|
| Required Credentials | Experience with eCTD publishing, life sciences or pharmaceutical background, familiarity with publishing tools | Regulatory knowledge, degree in life sciences, understanding of regulatory submissions |
| Work Environment | Primarily document publishing, review, and formatting tasks in a remote setting | Regulatory strategy, submission planning, and compliance activities often involving cross-functional teams |
| Employer & Industry Usage | Pharmaceutical, biotech, and CRO companies focusing on electronic submissions | Pharmaceutical companies, regulatory agencies, and consulting firms |
The main difference is that Remote Ectd Publishers focus on preparing and formatting electronic submissions, while Remote Regulatory Affairs Associates handle broader regulatory strategies and compliance. Both roles require industry-specific knowledge but differ in scope and responsibilities.
What are some common challenges Remote eCTD Publishers face, and how can they be managed effectively?
Remote eCTD Publishers often encounter challenges such as coordinating with cross-functional teams across time zones, ensuring version control, and managing tight regulatory submission deadlines. To address these, strong organizational skills, proactive communication, and familiarity with collaboration tools are essential. Leveraging secure document management systems and establishing clear workflows can also help maintain accuracy and compliance, while regular virtual check-ins with team members foster efficient information sharing and problem-solving.
What are popular job titles related to Remote Ectd Publisher jobs in Basking Ridge, NJ? For Remote Ectd Publisher jobs in Basking Ridge, NJ, the most frequently searched job titles are:
What job categories do people searching Remote Ectd Publisher jobs in Basking Ridge, NJ look for? The top searched job categories for Remote Ectd Publisher jobs in Basking Ridge, NJ are:
What cities near Basking Ridge, NJ are hiring for Remote Ectd Publisher jobs? Cities near Basking Ridge, NJ with the most Remote Ectd Publisher job openings:
Contractor
Posted 28 days ago
Job description
Hi,
My name is Karthik Mutyala, from Stark Pharma Solutions Inc, we are hiring talents for our client. I am working on Veeva Vault RIM Consultant position right now. Please send me your updated resume if you have relevant experience and interested in this position. The detailed job description is as follows
Position: Regulatory Business Analyst - Veeva Vault RIM
Location: Remote
Duration: 6-Month Contract
Experience: 5–6 Years
Job Overview
We are seeking a Regulatory Business Analyst with strong expertise in Veeva Vault RIM to support regulatory operations, data remediation, system enhancements, and business process optimization. The ideal candidate will have experience with regulatory information management, validation activities, and digital transformation initiatives within a regulated life sciences environment.
Key Responsibilities
- Support configuration, maintenance, and business processes within Veeva Vault RIM.
- Perform regulatory data remediation and ensure data quality and integrity.
- Support IDMP, eCTD, and regulatory submission processes.
- Manage integrations between Veeva Vault Quality and Veeva Vault RIM.
- Develop and monitor RIM reports, dashboards, and KPIs.
- Coordinate UAT, review test scripts, and support system validation activities.
- Create and maintain SOPs, training materials, and user documentation.
- Collaborate with cross-functional teams on AI/GenAI, automation, and digital transformation initiatives.
- Support continuous process improvements within regulatory systems.
Required Qualifications
- Bachelor's degree in Life Sciences, Information Systems, or a related field.
- 5+ years of experience as a Business Analyst supporting Regulatory Affairs systems.
- Strong hands-on experience with Veeva Vault RIM (configuration, data model, and business process support).
- Experience with data remediation, IDMP, eCTD, and SDLC.
- Knowledge of Veeva Vault Quality–RIM integrations.
- Experience supporting validation activities, including UAT and test script reviews.
- Strong documentation skills with experience creating SOPs and training materials.
- Exposure to AI/GenAI, automation, or digital transformation initiatives.
- Familiarity with eCTD publishing solutions; eCTD 4.0 experience is a plus.
I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.
Please follow Stark Pharma Solutions on LinkedIn for the latest job updates: https://www.linkedin.com/company/99455976/
Thank you,
Karthik Mutyala
Recruiting Manager
Stark Pharma Solutions Inc
Email: karthik@starkpharma.com
15 Corporate Place S, Suite 350,
Piscataway, New Jersey 08854
www.starkpharma.com