Remote Clinical Trial Manager – Oncology & Rare Diseases

Precision Medicine Group, LLC.

Australia

Remote

AUD 130,000 - 170,000

Full time

22 hours ago
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Job summary

Precision for Medicine seeks a Clinical Trial Manager to lead the operational aspects of clinical studies across international sites. You will ensure adherence to protocols, SOPs, ICH-GCP, and regulatory requirements while serving as the primary point of contact for clients and study teams.

You will develop essential study documents, manage budgets, coordinate site feasibility, and train CRAs/vendor staff. This role requires strong communication, travel flexibility, and collaboration with

Qualifications

  • Bachelor's degree or equivalent in science/health; advanced degree preferred.
  • Minimum 5–8 years of clinical research experience with significant monitoring.
  • Experience with Microsoft Office products.
  • Excellent communication and interpersonal skills; ability to travel domestically and internationally.

Responsibilities

  • Serve as the clinical trial lead for planning, conduct and oversight of the operational portion of clinical studies.
  • Primary clinical point of contact with the client; collaborate on monthly invoicing and budget variance.
  • Develop study documents (clinical plans, ICF templates, CRF guidelines, study trackers).
  • Identify and develop training needs for CRAs and vendors; present at Investigator Meetings.
  • Drive site feasibility and develop country recruitment/retention strategy.
  • Oversee submissions to authorities and ethics committees; ensure regulatory compliance.

Skills

Clinical trial management
Budget management
Stakeholder management
Regulatory compliance
Cross-functional leadership

Education

Bachelor's degree in Life Sciences
Advanced degree preferred

Tools

CTMS
Microsoft Office

Job description

Precision for Medicine seeks a Clinical Trial Manager to lead the operational aspects of clinical studies across international sites. You will ensure adherence to protocols, SOPs, ICH-GCP, and regulatory requirements while serving as the primary point of contact for clients and study teams.

You will develop essential study documents, manage budgets, coordinate site feasibility, and train CRAs/vendor staff. This role requires strong communication, travel flexibility, and collaboration with

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