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Senior Regulatory Start Up Associate

Novotech
NovoTech
1-3 years
Not Disclosed
10 Jan. 22, 2026
Job Description
Job Type: Full Time Hybrid Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Senior Regulatory Start-Up Associate

Location: Sydney, New South Wales, Australia
Employment Type: Full-Time
Work Model: Hybrid (2 days onsite, 3 days remote)
Job ID: 3674
Industry: Clinical Research | Regulatory Affairs | CRO
Experience Required: 1–3 years
Posting Date: January 15, 2026

About the Company

Novotech is a global full-service Contract Research Organization (CRO) headquartered in Sydney, Australia, with operations across Asia-Pacific, North America, and Europe. With more than 3,000 employees, 34 offices, and over 5,000 site partnerships, Novotech provides comprehensive clinical development services across all trial phases and therapeutic areas. The organization operates under ISO 27001 and ISO 9001 certified quality management systems, ensuring the highest standards of regulatory compliance, data security, and operational excellence.

Position Overview

Novotech is seeking a Senior Regulatory Start-Up Associate to support clinical trial start-up activities in Australia. This role is responsible for planning, preparing, reviewing, and managing country- and site-level ethics and regulatory authority submissions to ensure timely clinical trial approvals. The position plays a critical role in aligning regulatory timelines with project deliverables while maintaining full compliance with ICH-GCP and local regulatory requirements.

This is a hybrid role based in Sydney, offering flexibility while enabling close collaboration with regulatory and project teams.

Key Responsibilities

  • Serve as the primary regulatory point of contact for the Regulatory Start-Up Manager (RSM) and/or Project Manager (PM) during study start-up activities.

  • Provide expert guidance on Australian regulatory requirements, ethics committee processes, and local clinical trial approval pathways.

  • Prepare, review, and manage regulatory and ethics submissions in accordance with ICH-GCP, applicable SOPs, and project plans.

  • Track submission timelines, approval metrics, and regulatory milestones for Regulatory Authorities, Ethics Committees, and Institutional Review Boards.

  • Ensure submission and approval timelines are met and accurately documented in internal tracking systems, including planned and actual dates.

  • Liaise with investigative sites and external regulatory bodies regarding regulatory and ethics-related activities as required.

  • Stay current with regulatory updates, guideline changes, and evolving local and international regulatory practices impacting clinical trial approvals.

Required Qualifications

Education:

  • Graduate degree in Clinical Research, Pharmacy, Life Sciences, or a related discipline.

Experience:

  • Minimum 1–3 years of regulatory start-up or clinical research experience within a CRO, pharmaceutical company, or clinical/hospital environment in Australia.

Skills & Competencies:

  • Strong working knowledge of ICH-GCP and Australian regulatory and ethics submission processes.

  • Excellent written and verbal English communication skills.

  • Ability to manage multiple regulatory submissions across concurrent projects.

  • Proficiency in working with multiple IT systems, clinical trial databases, and document management platforms.

  • Strong organizational, analytical, and stakeholder management skills.

Why Join Novotech

Novotech offers a collaborative, inclusive, and people-focused workplace culture. Employees benefit from hybrid working arrangements, paid parental leave for both parents, flexible leave entitlements, wellness initiatives, and continuous professional development programs. The organization actively promotes diversity, equity, and inclusion and encourages applications from individuals of all backgrounds, including those identifying as LGBTIQ+, individuals with disabilities, and those with caring responsibilities.

As a Circle Back Initiative Employer, Novotech is committed to responding to every applicant.

About the Team

Novotech’s regulatory teams combine deep therapeutic expertise with strong regional regulatory knowledge to support global clinical programs. Team members work in empowered, collaborative environments that value strategic thinking, proactive decision-making, and partnership-driven execution, supported by senior leadership.

Application Process

Interested candidates are encouraged to apply with an updated CV highlighting regulatory start-up experience, Australian regulatory expertise, and clinical trial submission exposure. Applications are reviewed on a rolling basis.