Principal Regulatory Operations Publisher

Jobgether; Canada; Remote; CAD 120,000 - 180,000; Full time

Benefits offered by this job

Fully remote

Remote India eligible

Competitive salary

Bonus opportunities

Flexible time off

Medical insurance

Tuition reimbursement

Retirement plans

Global collaboration

Job summary

Jobgether is seeking a Principal Regulatory Operations Publisher in Canada to lead complex regulatory publishing projects and oversee electronic submission readiness. You will collaborate with Medical Writing, Biostatistics, Programming and Regulatory Affairs to ensure high-quality, compliant documents.

You will mentor colleagues, provide technical guidance, and support global submissions in a flexible, international team. Strong English communication and post-marketing experience are preferred.

Qualifications

• Bachelor's degree required in a scientific field.
• 8+ years of regulatory publishing experience in CRO/pharma/biotech settings.
• Proficiency with publishing software (eCTDmanager, DocuBridge, eCTDXpress).
• Strong Word formatting and template skills; English writing skills.

Responsibilities

• Lead regulatory publishing projects from planning to completion.
• Finalize and publish regulatory documents for electronic submissions.
• Coordinate with cross-functional teams for submission readiness.
• Manage major regulatory dossiers and submission amendments.
• Ensure compliance with publishing standards and guidelines.
• Mentor junior team members and drive process improvements.
• Support FDA/EMA submissions and post-marketing activities.

Skills

Regulatory publishing

Project leadership

Cross-functional collaboration

Attention to detail

Education

Bachelor's degree in a scientific discipline

Tools

eCTDmanager

DocuBridge

ISIToolbox

Adobe Acrobat

EndNote

Job description

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Principal Regulatory Operations Publisher based in Canada.

Take on a senior-level role within a global clinical research and regulatory environment, helping accelerate the development and approval of life-changing therapies. As a Principal Regulatory Operations Publisher, you will independently lead complex regulatory publishing projects and ensure the successful preparation and finalisation of electronic regulatory submissions. You will collaborate closely with Medical Writing, Biostatistics, Programming, and Regulatory Affairs teams to deliver high-quality, compliant documentation. Beyond project execution, you will provide technical guidance, mentor colleagues, and serve as a trusted expert for regulatory publishing challenges. This opportunity offers the chance to contribute to impactful clinical research programmes across therapeutic areas, including oncology and rare diseases. Join a collaborative, international team that values expertise, innovation, and flexible working arrangements.

Accountabilities

• Independently lead regulatory publishing projects from planning through completion, ensuring timely and successful delivery.
• Manage the finalisation, formatting, quality control, and publishing of regulatory documents for electronic submissions.
• Coordinate with Medical Writing, Biostatistics, Programming, Regulatory Affairs, and other cross-functional teams to ensure submission readiness.
• Independently manage major regulatory dossiers and submission amendments of varying complexity and scope.
• Ensure regulatory documents comply with applicable publishing standards, technical requirements, and submission guidelines.
• Represent the Regulatory Operations function in critical business activities and cross-functional project discussions.
• Serve as a technical escalation point for regulatory publishing questions, troubleshooting, and complex document-related challenges.
• Mentor and support junior team members, sharing technical expertise and promoting best practices.
• Contribute to continuous improvement initiatives within regulatory publishing workflows and operational processes.
• Support global regulatory submissions, including FDA and EMA submissions, as well as post-marketing regulatory activities.

Requirements

• Bachelor's degree, preferably in a scientific discipline.
• At least 8 years of relevant regulatory publishing experience within a contract research organisation (CRO), pharmaceutical company, biotechnology organization, or clinical research setting.
• Advanced proficiency in Adobe Acrobat, ISIToolbox, and regulatory publishing software such as eCTDmanager, DocuBridge, or eCTDXpress.
• Strong expertise in Microsoft Word formatting, including advanced use of styles and templates, as well as familiarity with EndNote.
• Proven ability to independently manage complex regulatory publishing projects and lead project teams effectively.
• Experience with global regulatory submissions, including FDA and EMA requirements, is highly desirable.
• Familiarity with post-marketing submissions is preferred.
• Strong understanding of medical and statistical terminology.
• Excellent written and verbal English communication skills, including writing, editing, and document review.
• Exceptional attention to detail and commitment to accuracy, consistency, and regulatory compliance.
• Strong interpersonal, organisational, and stakeholder-management skills.
• Ability to work collaboratively across multidisciplinary teams and act as a consultative regulatory publishing partner.
• Demonstrated leadership, mentoring, and problem-solving capabilities.

Benefits

• Fully remote working opportunities, including eligibility for remote work from India.
• Competitive compensation, with salary determined according to location, skills, experience, education, and relevant market conditions.
• Performance-based bonus opportunities, where applicable.
• Flexible time-off arrangements.
• Paid holidays.
• Medical insurance, depending on location.
• Tuition reimbursement and professional development support, where available.
• Retirement plans, depending on regional eligibility.
• Opportunity to contribute to global clinical research programmes and support the development of life-changing therapies.
• Collaborative and inclusive international working environment.
• Career development opportunities within a specialised regulatory operations and clinical research setting.