Regulatory Affairs Job at Parexel | Apply Now
Regulatory affairs job opportunities are growing rapidly in the global pharmaceutical industry, and Parexel is currently hiring a Regulatory Affairs Associate Publishing professional for a remote role based in Argentina. This exciting life sciences job is ideal for candidates with experience in regulatory publishing, document management, and eCTD submissions. If you are looking for Parexel careers with strong growth potential in regulatory affairs, this opportunity could be the perfect fit.
- Job Position: Regulatory Affairs Associate Publishing
- Location: Argentina with a remote work setup
- Job ID:Â R0000039539
- Job Category:Â Regulatory Affairs
About the Company
Regulatory affairs job seekers looking for global pharmaceutical and clinical research opportunities can explore exciting openings at Paarexel. The company is a leading clinical research organization that provides regulatory, consulting, and clinical development services to the pharmaceutical and biotechnology industries worldwide. Parexel careers are known for offering flexible work opportunities, innovation-driven environments, and strong professional growth in the life sciences sector.
Regulatory Affairs Job Description
Regulatory affairs role responsibilities at Parexel include developing, publishing, and supporting the publishing of regulatory submissions to global health authorities in alignment with established standards, requirements, and organizational commitments. The selected candidate will ensure all submissions are prepared in high-quality, compliant formats while supporting both internal and external stakeholders. This life sciences job also involves performing related publishing activities as needed and maintaining compliance with electronic submission requirements for global regulatory agencies.
Qualifications
Regulatory affairs job candidates should meet the following requirements:
- 1–3 years of experience in regulatory publishing or document management within the pharmaceutical industry
- Experience working with XML or other structured document formats
- Foundational knowledge of eCTD structure and electronic submission requirements for global health authorities including FDA, EMA, and Health Canada
- Proficiency with regulatory publishing systems such as Veeva, Extedo, Insight, DXC, or comparable platforms
- Solid understanding of eCTD structure, submission standards, and regulatory guidelines
- Exceptional attention to detail with the ability to manage complex documentation and meet demanding timelines
Education Requirement
- Bachelor’s degree in Life Sciences, Regulatory Affairs, or a related field
- Equivalent work experience may also be considered
Preferred Qualifications
- Familiarity with end-to-end submission lifecycle maintenance processes
- In-depth knowledge of FDA and international regulatory agency requirements
- Experience with document control or compliance-driven workflows
- Strong background in document preparation and formatting
Required Skills
- Proficiency in Microsoft Word and Adobe Acrobat for document formatting, hyperlinking, and submission preparation
- Ability to work effectively in a cross-functional team environment
- Strong multitasking skills under tight deadlines
- Ability to quickly learn new software tools and systems
- Effective written and verbal communication skills
Key Responsibilities – Regulatory Affairs Job
Regulatory affairs job duties for this role include:
- Develop and publish regulatory submissions for global health authorities
- Support the publishing of compliant electronic submissions
- Ensure documentation aligns with organizational commitments and regulatory standards
- Prepare submissions in high-quality formats
- Collaborate with internal and external stakeholders
- Support regulatory publishing activities and submission maintenance processes
- Work with structured document formats including XML
- Manage complex documentation within strict timelines
Why Consider Parexel Careers?
Regulatory affairs role opportunities at Parexel provide professionals with exposure to global regulatory systems, innovative publishing technologies, and international healthcare projects. This life sciences job is ideal for candidates seeking remote jobs in Argentina while building expertise in regulatory submissions and pharmaceutical compliance.
