Unlock remote pharma jobs in Argentina with Parexel’s Regulatory Affairs Associate role. Leverage your expertise in regulatory strategies for biopharma success. Apply now for flexible, impactful pharmaceutical careers.
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About the Company
Parexel is a leading biopharmaceutical services company founded in 1982, with over 21,000 employees across more than 50 countries. Specializing in accelerating drug development and delivery, it offers end-to-end solutions in clinical research, regulatory affairs, and consulting. Parexel’s global presence ensures innovative, data-driven strategies that navigate complex regulatory landscapes.
Committed to compliance, collaboration, and growth, the company empowers clients to bring therapies to market faster through strategic acquisitions and advanced technologies.
Job Details
- Company Name: Parexel
- Experience: 1-2 years in preparing regulatory dossiers for Argentina (Clinical Trials Applications and maintenance); initial years in industry-related environment
- Qualification: Minimum Bachelor’s Degree in a Scientific Discipline
- Location: Argentina, Remote
- Work Type: Remote (full-time)
Job Description
Parexel Consulting seeks a Regulatory Affairs Associate to support biopharmaceutical and medical device clients in regulatory navigation. This remote role in Argentina focuses on strategy development and compliance for faster market access. Join a team valuing innovation, diverse therapeutic areas, and professional growth in pharmaceutical careers.
Regulatory Affairs Associate
- Department: Regulatory Affairs
- Market: Global (Argentina-based, remote)
- Role: Execute projects, deliver consulting services, and manage client relationships under guidance
- Experience: 1-2 years in regulatory dossiers for Argentina; initial industry experience
- Education/Qualification: Minimum Bachelor’s Degree in a Scientific Discipline
Skills/Qualifications
- Project management knowledge and client-focused approach
- Results orientation and teamwork/collaboration skills
- Consulting skills with excellent interpersonal and intercultural communication (written and verbal)
- Critical thinking and problem-solving abilities
- Proficiency in local language and extensive English knowledge
- Basic understanding of consulting models and regulatory services
Key Responsibilities
- Work effectively in team environments within project guidelines
- Prioritize tasks to achieve project outcomes with SME guidance
- Produce quality work meeting client and lead expectations
- Serve as Project Lead for small projects or Work Stream Lead
- Manage project planning, financials, and client interactions
- Implement consulting methodologies under supervision
- Identify issues and needs to senior colleagues
- Network for business development and communicate leads
- Meet metrics, complete administrative tasks, and pursue self-development
Benefits/Perks
- Remote work flexibility for work-life balance
- Continuous learning through mentorship and challenging assignments
- Exposure to diverse clients and therapeutic areas
- Collaborative, innovative culture fostering growth
- Global opportunities in regulatory affairs and consulting
How to Apply
Apply directly for Job ID R0000036174 via Parexel’s career portal at Parexel Careers. Submit your resume and cover letter for a streamlined process.
Verified Work From Home Job Post
The post is released by the Parexel Career page. Click here to visit the post
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For more remote pharma jobs in Argentina, visit Pharma Recruiter. Seize this chance to advance your regulatory career—apply today!
Why You Should Join
Parexel cultivates a supportive, dynamic culture emphasizing collaboration, innovation, and continuous learning. As a remote team member, I enjoy long-term stability in a growing biopharma leader, with mentorship from experts and exposure to cutting-edge projects.
Thrive in a compliance-focused environment that rewards strategic thinkers, delivering real impact on global therapies while building lasting industry networks.
FAQs
What eligibility is required for this remote pharma job?
A Bachelor’s in a scientific discipline is minimum, plus 1-2 years in Argentina regulatory dossiers and initial industry experience. Strong English proficiency is essential for regulatory affairs roles.
How does Parexel’s application process work?
Apply online via the career portal with your resume and details. Expect a review focused on fit for consulting and regulatory expertise, ensuring transparency in your pharmaceutical career journey.
What growth opportunities are available?
Gain skills through project leadership, mentorship, and diverse assignments. Advance in regulatory strategy amid global expansion, ideal for QA jobs and consulting in pharma.
Are walk-in interviews offered for this position?
No walk-in options; all applications are remote via the portal. Explore Pharma Recruiter for other regulatory affairs jobs in Argentina.