Clinical Trial Manager - APAC - Onco

Worldwide; Australia; Remote; AUD 90,000 - 130,000; Full time

Job summary

Worldwide Clinical Trials is hiring a Clinical Trial Manager for APAC, remotely based in Australia. You will lead site management and monitoring across multiple studies from initiation through close-out, coordinating with project teams and sponsors to ensure quality and timelines.

The role requires 3+ years as CRA or 5+ years with a two-year degree, strong leadership, GCP/ICH knowledge, and proficiency with EDC/CTMS/eCRF/IxRS. English fluency is essential.

Qualifications

• Bachelor's degree or higher in life sciences or related field; clinical research experience preferred.
• Minimum three years as a Senior CRA or five years with a two-year degree; at least six months as a Trial Manager/Lead CRA.
• Strong leadership to guide remote clinical teams across studies.
• Deep knowledge of clinical research processes, GCP, ICH guidelines, FDA/EU regs, and local requirements.
• Experience developing monitoring strategies, site performance, and deliverables.
• Proficiency with MS Office and clinical systems (EDC/CTMS/eCRF/IvRS/IxRS).
• Excellent planning, organizational, presentation, communication, negotiation, and stakeholder skills.
• Fluent in English.

Responsibilities

• Lead site management and monitoring across studies from initiation to close-out.
• Partner with Project Management to set monitoring strategies and targets.
• Provide leadership and clinical guidance to CRAs and site teams.
• Act as primary site management representative to sponsors, investigators, and audits.
• Oversee monitoring quality, site performance, protocol compliance, and deliverables.
• Drive patient recruitment and monitor enrollment performance.
• Review study metrics to improve data quality and operations.
• Identify and mitigate study risks and site issues.
• Ensure Trial Master File readiness and regulatory compliance.

Skills

Leadership

Project management

Clinical trial oversight

Communication

Stakeholder management

Remote team leadership

GCP knowledge

English proficiency

Education

Bachelor's degree in life sciences or related field

Tools

EDC

CTMS

eCRF

IVRS

IxRS

Job description

Clinical Trial Manager - APAC - OncoWe use cookies to improve your browsing experience and help us improve our websites. We have carefully selected third parties that use cookies to achieve purposes illustrated in the cookie policy. For more information. Read more about online privacy statement. By closing this banner or continuing to browse our website, you agree to our use of such cookies.https://www.worldwide.com/privacy-statement-terms-of-use/online-privacy-statement/# Discover a world of difference at Worldwide.## Clinical Trial Manager - APAC - OncoApply: Remote: Virtual Australia: Full time: Posted Today: JR103259Join a global Contract Resource Organization (CRO) where innovation meets purpose. At **Worldwide Clinical Trials**, we're driven by a shared commitment to improving lives through high-quality clinical research. Our teams are empowered to think creatively, take ownership, and deliver meaningful work that helps bring life-changing therapies to patients around the world. With more than 4,000 professionals across the globe, we foster a collaborative and inclusive environment where diverse perspectives are valued, growth is encouraged, and every contribution makes an impact. Whether you're building your career or bringing years of experience, you'll have the opportunity to learn, grow, and help shape the future of clinical research. Make an Impact as a Clinical Trial Manager at Worldwide Play a pivotal role in delivering high-quality clinical research by leading site management activities across clinical studies from start-up through close-out. In this role, you'll guide and coordinate clinical monitoring teams, ensuring studies are executed efficiently, compliantly, and with a strong focus on quality and patient outcomes.You'll serve as a key partner to project teams, sponsors, and clinical research sites, driving monitoring strategy, overseeing operational performance, and proactively managing risks. Your leadership will help ensure studies remain on track, data quality is maintained, and sites receive the support needed to successfully deliver study objectives.Working across multiple stakeholders and geographic regions, you'll bring together clinical expertise, operational oversight, and team leadership to achieve timely and successful study delivery. Where You'll Work This is a REMOTE role open to candidates based in Australia. You will collaborate with global teams across multiple time zones.Travel will be required as part of this role. A valid passport and driver's license are required. What You'll Do * Lead and coordinate site management and monitoring activities across clinical studies from initiation through close-out.* Partner with Project Management to establish monitoring strategies, operational targets, and study execution plans aligned with project goals.* Provide leadership, guidance, and clinical expertise to Clinical Research Associates and site management team members throughout the study lifecycle.* Serve as the primary site management representative for sponsors, investigators, study teams, audits, inspections, and key project meetings.* Oversee monitoring quality, site performance, protocol compliance, and timely completion of monitoring deliverables.* Drive patient recruitment efforts, monitor enrollment performance, and support site-level strategies to keep recruitment on target.* Review study metrics, trends, and analytics to improve site performance, data quality, and operational effectiveness.* Identify, escalate, and help resolve study risks and site issues while implementing proactive mitigation strategies.* Ensure Trial Master File compliance, inspection readiness, and adherence to study protocols, SOPs, regulatory requirements, and quality standards.What You'll Bring * Bachelor's degree (or equivalent) in biological, physical, health, nursing, life sciences, or a related field, with relevant clinical research experience; alternatively, a two-year degree with extensive Senior Clinical Research Associate experience.* Minimum three years of experience as a Senior Clinical Research Associate (or equivalent), or five years with a two-year degree, and at least six months of experience supporting or functioning as a Clinical Trial Manager, Lead CRA, or equivalent role.* Strong leadership experience with the ability to guide, motivate, and support remote clinical teams.* Extensive knowledge of clinical research processes, monitoring practices, Good Clinical Practice (GCP), ICH Guidelines, FDA and/or EU regulations, and local regulatory requirements.* Experience developing and implementing monitoring strategies, overseeing site performance, and managing clinical operations deliverables.* Proficiency with Microsoft Office and clinical systems including EDC, CTMS, eCRF, IVRS, and IxRS platforms.* Excellent planning, organizational, presentation, communication, negotiation, problem-solving, and stakeholder management skills.* Proficiency in English.