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Parexel
Parexel Regulatory Affairs Consultant – Core Team Recruitment 2026: Apply Online
Regulatory Affairs Consultant – Core Team
Experience Required
Several years in an industry-related environment
Salary / Package
Competitive & Industry Standard
Work Mode
Remote / Flexible
Openings
1
Job Overview
- As part of Parexel Consulting, help biopharmaceutical and medical device companies navigate complex regulatory landscapes.
- Develop and implement regulatory strategies leveraging scientific, technical, and regulatory expertise.
- Partner with a diverse group of clients across various therapeutic areas and product types.
- Ensure project execution aligns with quality standards, timelines, and contractual scope.
- Maintain compliance, prepare technical documentation, and support business development opportunities.
Key Job Details
| Company Name | Parexel |
| Job Role | Regulatory Affairs Consultant – Core Team |
| Experience | Several years in an industry-related environment |
| Salary Range | Competitive & Industry Standard |
| Job Type | Full-time / Remote |
| Work Mode | Remote / Flexible |
| Openings | 1 |
| Job Location | Australia – North Ryde / Remote |
Key Responsibilities
- Work within a team or independently to deliver technical consulting services within areas of expertise.
- Prioritize work and define steps needed to achieve specified project outcomes and milestones.
- Interact with clients professionally, managing project reporting, quality control, and risk identification.
- Ensure project financial tracking, forecasting, and proper resource utilization.
- Mentor junior staff and participate in internal initiatives or training compliances.
Requirements & Qualifications
- Solid knowledge in Regulatory Affairs Activities, focusing on CTAs (Phase I-IV) for various therapeutic areas.
- Proficient in relevant regulations and regional submission processes.
- Preferred experience in early phase studies, medical devices, GMOs, or biological drugs.
- Ability to work autonomously as well as collaboratively in a remote team structure.
Required Skills
- Project management knowledge and results-oriented mindset
- Client-focused approach with excellent consulting skills
- Exceptional interpersonal and intercultural communication skills (written and verbal)
- Critical thinking and advanced problem-solving capabilities
About Parexel
Parexel is a leading clinical research organization (CRO) providing biopharmaceutical and medical device clients worldwide with comprehensive clinical development and regulatory consulting services driven by a patient-first mission.
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Frequently Asked Questions
Q: What are the core educational requirements for the Regulatory Affairs Consultant role?
A: Candidates must hold at least a Bachelor’s Degree in a Scientific or Technical Discipline, with Advanced Degrees being preferred.
Q: Is remote work supported for this position?
A: Yes, this position offers flexible remote working options while remaining part of a dynamic global team.
Q: What experience is preferred for this role?
A: Experience with Clinical Trial Authorizations (CTAs Phase I-IV), regulatory activities, and familiarity with regional regulations (such as Australia/New Zealand) is preferred.
Q: How can I apply for this position?
A: You can apply directly online through the official Parexel Workday careers link provided in the job posting.
Q: What does Parexel do as an organization?
A: Parexel is a global clinical research organization that helps pharmaceutical and biotech companies accelerate the development and approval of life-changing medicines.
Disclaimer: This job post is prepared by collecting data from the official career page of Parexel. We are not direct recruiters or representatives. Candidates should carefully review the requirements and policies on the company’s portal before initiating an application.