Looking for pharma jobs in clinical research? Explore this Regulatory Start-Up Associate role—ideal for professionals seeking pharmaceutical careers in India and global CRO opportunities.
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About the Company
This opportunity is with a global clinical research organization (CRO) known for delivering high-quality clinical trial services worldwide. The company emphasizes innovation, regulatory compliance, and operational excellence.
With a strong global presence, it supports pharmaceutical and biotechnology companies in bringing new therapies to market efficiently. Employees benefit from a collaborative environment, continuous learning, and exposure to international clinical research projects.
Job Details
- Company Name: Novotech
- Experience: Varies by role (Associate I/II level)
- Qualification: Life Sciences / Pharmacy or related field
- Location: Australia
Job Description
Novotech is hiring Regulatory Start-Up Associates to support clinical trial start-up activities. This role focuses on regulatory submissions, ethics approvals, and compliance with global clinical research standards.
Regulatory Start-Up Associate I/II
- Department: Clinical Research / Regulatory Affairs
- Market: Global Clinical Trials
- Role: Regulatory submission planning and execution
- Experience: Associate level (I/II)
- Education/Qualification: Life Sciences, Pharmacy, or related discipline
Skills/Qualifications
- Strong understanding of ICH-GCP guidelines
- Knowledge of regulatory authority submission processes
- Experience with ethics committees and IRB submissions
- Ability to manage timelines and multiple stakeholders
- Strong communication and coordination skills
- Knowledge of country-specific regulatory requirements
- Problem-solving and action-oriented mindset
Key Responsibilities
- Prepare and submit regulatory and ethics documents
- Ensure compliance with ICH-GCP and local regulations
- Manage submission timelines and approval tracking
- Coordinate with sites and project stakeholders
- Provide regulatory guidance to project teams
- Maintain accurate submission records and systems
- Track approvals and update project databases
- Act as primary contact for start-up activities
Benefits/Perks
- Competitive salary and global exposure
- Career growth in clinical research
- Learning and development opportunities
- Work with international regulatory teams
- Inclusive and collaborative work culture
- Exposure to global clinical trials
How to Apply
Verified Post
Verification: To confirm the legitimacy of this posting, you can view the original announcement on the Novotech career page.
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Interested candidates should apply through the official company careers portal. You can also explore similar opportunities on Pharma Recruiter: https://pharmarecruiter.in
Apply now to grow your career in clinical research and regulatory affairs.
Why You Should Join
This role offers excellent exposure to global clinical trial processes and regulatory systems. Employees gain hands-on experience with international submissions, regulatory compliance, and stakeholder management. It is an ideal opportunity for building a long-term career in clinical research and pharmaceutical development.
FAQs
Who can apply for this role?
Candidates with Life Sciences or Pharmacy backgrounds and regulatory knowledge can apply.
Is this a remote job?
The job location is Australia; work type is not specified.
How can I apply?
Apply via the official company careers portal or check Pharma Recruiter for updates.
What growth opportunities are available?
The role offers global exposure, skill development, and advancement in clinical research.
