Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as a Senior Regulatory Publishing Specialist – Make an Impact at the Forefront of Innovation. We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.
As part of our expert team, you’ll have the opportunity to ensure operational excellence that makes a real difference in organizational performance. As a Senior Regulatory Publishing Specialist, you will provide experienced strategic, expedient, and efficient preparation of client electronic submission deliverables and dossiers that meet current local, regional, and ICH regulatory and technical requirements. You will ensure successful regulatory review outcomes for product milestones. Additionally, you will serve in a quality review role and be responsible for the thorough review of documents created within or outside of the company to ensure quality standards meet or exceed client expectations.

What You’ll Do:

• Provides expertise in client submission deliverables supporting regulatory compliance.

• Prepares components of electronic regulatory submissions that meet the electronic document requirements set by regulatory guidance, publishing documents and submissions that work with sponsor and/or regulatory agency software programs, and meeting consistency and security issues, under general supervision of the Manager, Electronic Publishing.

• Maintains document life cycle for submission documents.

• Leads the development and implementation of project-specific processes for sponsors with unique technology requirements.

• May act as the company's liaison for regulatory submission with the sponsor and assist the company's project teams in executing regulatory submission strategies.

• Provides leadership by participating in training, skill development, and mentoring of other electronic submission personnel, as needed.

• Uses professional judgment to evaluate the publishing needs in relationship to the overall project timelines, quality and delivery.

• Engages other project team members, functional units or publishing management as necessary to deliver final product and resolve/mitigate identified issues or barriers to delivery.

• Acts independently within a project team or as the project team lead to evaluate and deliver publishing tasks

Education and Experience Requirements:

• Bachelor's degree or equivalent and relevant formal academic / vocational qualification

• Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5+ years).

In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Knowledge, Skills and Abilities:

• Strong knowledge of regulatory requirements and guidances for document management and electronic submissions

• Advanced knowledge of Microsoft (MS) Word, MS Excel, Adobe Acrobat, electronic document management systems, document publishing tools, publishing systems, eCTD validation and viewing tools

• Advanced knowledge of electronic templates and skilled in formatting and troubleshooting templates

• Ability to manage several complex projects in parallel and adapt to changing priorities

• Ability to exercise independent judgment in developing methods, techniques and evaluation of criteria using defined procedures and practices

• Ability to independently assess sponsor needs and work with project team members in producing compliant deliverables

• Ability to independently learn new technologies

• Advanced organizational skills and effective interpersonal skills

• Advanced analytical ability and problem-solving capabilities

• Strong knowledge of medical terminology, statistical concepts, and guidelines and requirements of the FDA and other international regulatory agencies

• Advanced editorial/proofreading skills

• Detail-oriented, thorough, and methodical

• Ability to create and follow timelines and conduct long-range planning

• Ability to multi task performing numerous single or complex tasks without ignoring overall objectives

• Ability to judge when to initiate changes and make final determinations in the presentation of data in accordance with regulatory guidelines and reviewers’ comments

• Ability to concentrate on the detail in a document without losing sight of the document as a whole

Join our team and take advantage of these great benefits! Apply now to learn more about the full range of benefits we offer.

• Health & Wellbeing: Join a company that prioritizes your health & wellbeing with comprehensive benefits, wellness programs, and an Employee Assistance Program providing confidential support for personal and work-related issues.

• Flexibility: Balance your work and personal life with flexible arrangements.

• Extra Leave: Benefit from generous leave policies, including the option to purchase additional leave, paid birthday leave, and company paid parental leave.

• Charitable Giving & Volunteering: Make an impact with paid volunteer time to support non-profit organizations that matter to you.

• Learning & Development: Advance your career with access to online courses via Thermo Fisher Scientific University Plus and LinkedIn learning, workshops, and mentorship programs for continuous learning and skill development.

Thermo Fisher Scientific Australia WGEA Employer of Choice for Gender Equality