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Parexel

End-to-end clinical trials and regulatory consulting

Regulatory Affairs Consultant - Core Team

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeNorth Ryde, AustraliaNo salary listedRemote

About the Job

Requirements

  • Knowledge of regulatory affairs activities, focusing on Clinical Trial Applications (CTAs) across Phase I–IV and various therapeutic areas.
  • Proficiency in regulations, ideally including some knowledge of New Zealand regulations.
  • Knowledge of project management.
  • A client-focused approach to work.
  • Results orientation.
  • Teamwork and collaboration skills.
  • Consulting skills.
  • Excellent written and verbal interpersonal and intercultural communication skills.
  • Critical thinking and problem-solving skills.
  • Proficiency in the local language and extensive working knowledge of English.
  • Several years of experience in an industry-related environment.
  • A minimum of a bachelor’s degree in a scientific or technical discipline.

Responsibilities

  • Deliver services within the technical area of expertise, independently or in a team, and liaise with senior colleagues on issues and conflicts.
  • Prioritize work and define steps to achieve project outcomes; identify opportunities to improve individual performance and project efficiency.
  • Use information from previous projects, client work, and colleagues to complete assigned project activities and produce quality work meeting project lead and client expectations.
  • Serve as project lead for small-scale projects or work streams and lead larger projects when acting as project lead.
  • Plan and set up projects, and work with the assigned Project Specialist or Project Manager to control project setup, forecasting, financial entries, and invoicing.
  • Act as the main client contact and ensure accurate project reporting.
  • Ensure the project team delivers work that meets client expectations for quality and timeliness; establish risk identification and issue-escalation procedures and ensure project-specific training compliance.
  • Manage project financials, including accurate revenue forecasts; ensure the project team understands and follows contract scope.
  • Identify change-in-scope or add-on business opportunities, complete timely project close-out activities, and alert management and account managers to follow-on business or scope changes.
  • Implement the organization’s consulting models and methodologies and provide technical or business consulting within the area of expertise.
  • Complete assigned work within project scope and objectives while considering issues that may affect project profitability.
  • Collaborate with colleagues and clients to identify and resolve technical and process issues, seeking guidance from senior colleagues when appropriate.
  • Interact professionally with multiple levels within client organizations and the company; assess client needs and develop processes and solutions.
  • Deliver assigned work and services that satisfy clients; prepare or deliver presentations with senior colleague support and deliver training when appropriate.
  • Mentor junior staff.
  • Build an industry network through project relationships and other industry experience; communicate potential new business leads to management and account managers.
  • Participate in project scoping calls or proposal preparation with support from senior colleagues.
  • Meet annual scorecard metrics and complete job-related administrative responsibilities, including timesheets, expense reports, CV maintenance, training compliance, deliverable archiving, and internal initiatives or mentoring as requested.
  • Define self-development activities to stay current in the industry, such as maintaining membership in a relevant industry or scientific/technical association.

Desired Qualifications

  • Experience with Phase I or early-phase studies; studies involving medical devices, genetically modified organisms, radiopharmaceuticals, or biological drugs; or labeling for investigational medicinal products.
  • Experience in quality documentation and chemistry, manufacturing, and controls (CMC) for investigational medicinal products.
  • An advanced degree.

About the Company

Parexel

End-to-end clinical trials and regulatory consulting

Parexel provides end-to-end clinical development services for pharmaceutical, biotechnology, and medical device clients from Phase I to Phase IV. Its offerings include clinical trial management, regulatory consulting, and biostatistical analysis to support the design, execution, and analysis of clinical studies. The company operates as a CRO, partnering with sponsors to manage trials, ensure regulatory compliance, and generate robust data for drug development. What sets Parexel apart is its breadth of services across the trial lifecycle, emphasis on quality and reliability, and industry recognition, along with a focus on patient-centric approaches and leadership in gender partnership. The company’s goal is to help clients bring new therapies to market efficiently and safely by delivering high-quality, compliant trial outcomes and data that support regulatory submissions.

Company size
10,001+
Company stage
Acquired
Total funding
$8.5B
Headquarters
Durham, NC
Founded
1982

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