Clinical Project Manager

Proclinical; Sydney; Presencial; AUD 120 000 - 150 000; Tempo integral

Resumo da oferta

Proclinical is seeking a Clinical Project Manager to oversee a portfolio of clinical trials, ensuring quality, compliance with GCP and NHMRC guidelines, and timely execution. You will lead a small team and collaborate with sponsors, CROs and study teams to deliver high-quality results.

The ideal candidate holds tertiary qualifications in health, social or biological sciences and has proven leadership, strong planning, stakeholder management, and proficiency in MS Office.

Qualificações

• Tertiary qualifications in health, social, or biological sciences.
• Knowledge of HREC and RGO processes, GCP, and NHMRC guidelines.
• Experience managing clinical studies, preferably in early-phase research.
• Team management experience in a clinical research setting.

Responsabilidades

• Plan, coordinate, and manage clinical trials to meet sponsor and protocol requirements within timelines.
• Develop project plans, track milestones, and ensure achievement of objectives.
• Ensure trial execution aligns with regulations, GCP, and SOPs.
• Facilitate communication between sponsors, CROs, and study teams.
• Define stakeholder responsibilities, study requirements, and key milestones.
• Lead, motivate, and develop a clinical trial team for high performance.
• Provide training and coaching to team members.

Conhecimentos

Leadership

Project mgmt

GCP knowledge

Stakeholder mgmt

Comms skills

MS Office

Formação académica

Tertiary qualification in health/sciences

Descrição da oferta de emprego

Ready to lead projects that bring life-changing treatments to the world? Join our client and assist in making a difference to clinical research.

Proclinical is seeking a Clinical Project Manager to oversee and deliver a portfolio of clinical trials with a focus on quality, compliance, and timely execution. In this role, you will lead a small team, ensuring adherence to protocol requirements, Good Clinical Practice (GCP), and standard operating procedures (SOPs). This position requires strong leadership, organizational, and communication skills to foster collaboration among stakeholders and drive successful trial outcomes.

Responsibilities:

• Plan, coordinate, and manage clinical trials to meet sponsor and protocol requirements within agreed timelines.
• Develop project plans, track milestones, and ensure the achievement of project objectives.
• Ensure clinical trial execution aligns with applicable regulations, GCP guidelines, and internal SOPs.
• Facilitate effective communication and collaboration between sponsors, CROs, and study teams.
• Clearly define stakeholder responsibilities, study requirements, and key milestones.
• Support the continuous improvement of clinical trial management processes and tools.
• Lead, motivate, and develop a clinical trial team to achieve high performance.
• Provide training and empower team members to take ownership of their responsibilities.
• Monitor team performance and provide coaching to ensure successful delivery of outcomes.
• Ensure team compliance with site-specific policies, procedures, and training requirements.
• Pursue personal development and maintain up-to-date training records.
• Perform additional responsibilities as discussed with the line manager or management.

Key Skills and Requirements:

• Strong organizational, planning, and time management skills with attention to detail.
• Ability to multitask and work effectively under pressure.
• Proactive problem-solving skills and confidence in decision-making.
• Excellent stakeholder management and relationship-building abilities.
• Strong written and verbal communication skills.
• High level of integrity, professionalism, and adaptability to changing environments.
• Proven leadership and team development skills.
• Proficiency in clinical assessment techniques and IT systems, including MS Office.
• Solid project management skills to handle multiple projects and resources.
• Tertiary qualifications in health, social, or biological sciences.
• Knowledge of HREC and RGO processes, GCP, and NHMRC guidelines.
• Experience managing clinical studies, preferably in early-phase research.
• Team management experience in a clinical research setting.
  

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