Clinical Trial Manager

TL;DR

Clinical Trial Manager (Oncology): Serves as the lead for planning, conducting, and overseeing operational aspects of clinical studies with an accent on protocol compliance, GCP standards, and regulatory requirements. Focus on developing site feasibility processes, enrollment strategies, clinical monitoring plans, and ensuring data quality and audit readiness.

Location: Remote, based in Australia or Singapore

Company

CRO integrating clinical trial execution with scientific knowledge, laboratory expertise, and advanced data sciences, with a strong focus on Oncology and Rare Disease.

What you will do

• Act as primary clinical point of contact with clients and lead internal clinical team meetings.
• Develop study documents, training materials, site feasibility lists, and recruitment/retention strategies.
• Oversee site start-up, enrollment, maintenance, close-out, submissions to authorities, and IP management.
• Implement eTMF, generate metrics reporting, and collaborate on CAPAs, audits, and data quality.
• Support business development, vendor management, and potentially assume project management responsibilities.

Requirements

• Based in Australia or Singapore with ability to travel domestically and internationally.
• Bachelor’s degree in science or health-related field (advanced degree preferred).
• 5-8 years of clinical research experience with significant clinical monitoring; Oncology (Phase I) in Australia preferred.
• Experience with Microsoft Office; excellent communication, organizational skills, and attention to detail.

Nice to have

• Line management experience.
• Proven competencies in clinical trial operations.

Culture & Benefits

• Equal Opportunity Employer committed to diversity and inclusion.
• Support for reasonable accommodations in application process.