- Location
- India-Bengaluru-Remote
- Workplace
- Remote
- Type
- full-time
- Department
- Healthcare
- Seniority
- Entry
- Experience
- 5+ years
- Education
- Bachelor
- Industry
- Healthcare
- Category
- Healthcare
- Role type
- Individual Contributor
- Environment
- Office
- Source
- Workday
Overview
As a Senior Regulatory Affairs Associate, you'll lead end-to-end planning, coordination, and execution of Clinical Trial Applications across EU CTR and Rest of the World regions. Your responsibilities include managing submission timelines, collaborating with cross-functional teams, applying regulatory expertise, and monitoring KPIs. You'll manage risks and complexities in global regulatory environments, build stakeholder relationships, and ensure high-quality, compliant submissions. The role requires a bachelor's degree in Life Sciences, Pharmacy, or related field, with minimum 5+ years of industry experience in pharmaceutical or CRO environments. You must have experience in Clinical Trial Application submissions and strong project management skills in a global/matrix environment.
Description
When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
Job Summary:
The Clinical Trial Submission Lead (CTSL) is responsible for end-to-end planning, coordination, and execution of Clinical Trial Applications (CTA) across EU CTR and Rest of the World (ROW) regions. This role ensures timely, high-quality, and compliant submissions through effective cross-functional collaboration, proactive risk management, and strong regulatory expertise.
Key Responsibilities:
- Lead end-to-end CTA project management across multiple studies and countries
- Plan, track, and deliver submissions aligned with timelines and regulatory requirements
- Manage risks, dependencies, and complexities in global regulatory environments
- Apply knowledge of EU CTR and ROW CTA requirements
- Manage core clinical and regulatory documentation
- Collaborate with cross-functional global teams
- Build and maintain stakeholder relationships and resolve conflicts
- Monitor KPIs related to timelines and deliverable quality
- Identify risks and lead quality investigations as needed
Qualifications & Experience:
- Bachelor’s degree in Life Sciences, Pharmacy, or related field
- Minimum 5+ years of industry experience in pharmaceutical, CRO, or similar
- Experience in Clinical Trial Application submissions (EU CTR & ROW)
- Strong project management experience in a global/matrix environment
- Familiarity with clinical trials and regulatory processes
Key Skills:
- Project Management & Execution
- Regulatory Knowledge (EU CTR & Global Submissions)
- Risk & Issue Management
- Stakeholder Engagement
- Strong communication and problem-solving skills
- Adaptability, resilience, and teamwork
Skills
Languages
Remote Scope
About Parexel
Parexel is a global clinical research organization dedicated to improving the world's health through clinical development solutions spanning clinical trials, regulatory, consulting, and market access.
