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Location
In office (Melbourne)
Seniority
Senior · 3+ years exp
Employment
Full-Time

Confirmed on the employer's own hiring board on Nov 6, 2026. First seen by Alion on Nov 1, 2026.

Overview
Company
Impact
Profile match
Planet Pharma is a global, professional staffing and recruitment company specializing in strategic solutions for the pharmaceutical, biotechnology, device and related industries.

Senior Project Manager - Clinical Trials

About the Opportunity

Our client is a fast-growing clinical research organisation committed to advancing clinical trial delivery across Australia. Through innovative and patient-centric approaches, they partner with sponsors, CROs, investigators and healthcare providers to deliver high-quality clinical research programs.

Due to continued growth, an exciting opportunity has arisen for an experienced Senior Project Manager to lead a portfolio of clinical trials and provide leadership to a team of Project Managers and Associate Project Managers.

The Role

As a Senior Project Manager, you will be responsible for the successful delivery of multiple clinical trial projects, ensuring operational excellence, financial oversight, stakeholder satisfaction, and team leadership.

You will act as a key liaison between sponsors, CROs, vendors, investigators and internal teams, while driving project performance, quality outcomes and continuous improvement initiatives.

Key Responsibilities

Project Leadership & Delivery

  • Lead multiple clinical trial projects simultaneously, ensuring studies are delivered on time, within budget and in accordance with quality standards.
  • Develop and maintain detailed project plans, timelines and resource allocation plans.
  • Act as the primary escalation point for project-specific issues and study deliverables.
  • Review new study opportunities and provide operational feasibility input.
  • Support study start-up activities, including budget development and contract-related operational planning.
  • Ensure effective communication and collaboration across cross-functional teams and external stakeholders.

Financial & Portfolio Management

  • Maintain oversight of study budgets, forecasting and financial performance.
  • Monitor project expenditure against approved budgets and contracts.
  • Ensure accurate and timely study billing and invoicing processes.
  • Track portfolio performance and identify financial risks, implementing mitigation strategies where required.
  • Support revenue forecasting and reporting activities.

Stakeholder Management

  • Build and maintain strong relationships with sponsors, CROs, investigators, vendors and internal stakeholders.
  • Provide regular project updates and performance reporting.
  • Proactively manage stakeholder expectations and resolve issues in a timely manner.
  • Gather and act on sponsor feedback to drive service excellence and continuous improvement.

People Leadership

  • Lead, mentor and develop Project Managers and Associate Project Managers.
  • Drive performance, engagement and career development across the project management team.
  • Support workforce planning, succession planning and talent development initiatives.
  • Ensure new team members receive effective onboarding and role-specific training.

Quality & Compliance

  • Ensure projects are conducted in accordance with ICH-GCP, applicable regulations and internal procedures.
  • Support CAPA management, quality initiatives and continuous improvement activities.
  • Participate in the development and review of SOPs, guidelines and operational processes.
  • Conduct periodic project reviews and audits to ensure compliance and operational excellence.

Patient Recruitment & Retention

  • Support patient recruitment strategies across studies.
  • Monitor recruitment performance and identify risks to enrolment targets.
  • Collaborate with operational teams and external referral networks to optimise participant engagement and retention.
  • Ensure a positive participant experience throughout the clinical trial lifecycle.

What We’re Looking For

Essential Requirements

  • Tertiary qualification in Life Sciences, Health Sciences or a related discipline.
  • Strong knowledge of ICH-GCP and clinical research regulations.
  • Minimum 3 years’ experience in clinical trial project management or a similar leadership role.
  • Demonstrated experience managing multiple clinical trial projects concurrently.
  • Excellent organisational, communication and stakeholder management skills.
  • Strong financial acumen with experience managing study budgets and project profitability.
  • Proven ability to lead, mentor and develop high-performing teams.
  • Ability to work effectively in a fast-paced and evolving environment.

Desirable Requirements

  • Experience managing Phase I or First-in-Human clinical trials.
  • Previous experience within a pharmaceutical, biotechnology, CRO or clinical research environment.
  • Postgraduate qualifications in Business, Management or Project Management.
  • Experience working within TGA, FDA and/or EMA regulated environments.

Key Competencies

Successful candidates will demonstrate:

  • Strong leadership and team development capabilities.
  • Strategic thinking and commercial awareness.
  • Excellent relationship-building and influencing skills.
  • High levels of accountability and ownership.
  • Strong problem-solving and decision-making abilities.
  • Exceptional communication and stakeholder engagement skills.
  • A continuous improvement mindset with a focus on quality and operational excellence.
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